Clinical Operations Jobs in Pharma & Biotech
56
Open Positions
7
Remote Jobs
50
With Salary Data
Clinical Operations professionals manage and execute clinical trials in pharmaceutical and biotech settings. These roles typically require experience in clinical research methodology and strong project management skills.
Key positions include:
- Clinical Research Associate (CRA)
- Clinical Trial Manager
- Clinical Operations Manager
- Clinical Study Coordinator
- Clinical Data Manager
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Senior Clinical Research Scientist - JJMT ElectrophysiologyFresh
Oct 17 $89,000 - $143,750 Irvine, California, United States of America Apply →Senior Clinical Research Scientist - JJMT ElectrophysiologyApply →Fresh
Oct 17 $89,000 - $143,750
Irvine, California, United States of AmericaJohnson and Johnson is currently seeking a Senior Clinical Research Scientist to support the external research and evidence generation strategy needs of the Electrophysiology business. This role is based in Irvine, CA and reports to the office on assigned days 2-3 times per week. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full... | |
Senior Manager, Audit Intelligence CoordinatorFresh
Oct 17 $152,530 - $184,834; $142,550 - $172,741 Lawrence Township - NJ - US Apply →Senior Manager, Audit Intelligence CoordinatorApply →Fresh
Oct 17 $152,530 - $184,834; $142,550 - $172,741
Lawrence Township - NJ - USReporting to the Senior Director, Operations & Performance, the Senior Manager, Audit Intelligence Coordinator, is responsible for planning audits in support of the BMS Competitive Compliance Audit Program. This includes coordinating audits for internal sites, global suppliers, and various entities such as CMOs, APIs, raw materials, and external labs. This role involves planning, organizing, and scheduling audit assignments in accordance with the global audit plan. It also supports clinical and commercial business developments through due diligence audits and communicates any changes in the global audit plan to stakeholders and audit outsourcing partners. Utilizing data-driven insights, this role aims to enhance... | |
Recruiting Coordinator, Technical Recruiting (Temporary)Fresh
Remote
Oct 17 $52,000 - $65,000 US Remote Apply →Recruiting Coordinator, Technical Recruiting (Temporary)Apply →Fresh
Remote
Oct 17 $52,000 - $65,000
US RemoteHims & Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results. By normalizing health & wellness challenges and innovating on their solutions, we’re making better health outcomes easier to achieve. Hims & Hers is a public company, traded on the NYSE under the ticker... | |
Clinical Project CoordinatorFresh
Oct 17 $72,100 - $114,700 United States - California - Alameda Apply →Clinical Project CoordinatorApply →Fresh
Oct 17 $72,100 - $114,700
United States - California - AlamedaClinical Project Coordinator Our clinical research team has an opportunity for a Clinical Project Coordinator that will be working from the Alameda, California location. This individual will contribute to the coordination and execution of externally sponsored research projects. The role bridges scientific and operational functions, ensuring that project deliverables align with organizational objectives while maintaining compliance with internal standards and external regulations, operational, and strategic objectives. What You’ll Work On Assist in planning, coordinating, and monitoring research project activities, including timelines, deliverables, and risk management. Support the preparation, review, and organization of scientific content such as study protocols, abstracts,... | |
Principal CoreValve Therapy Development SpecialistFresh
Oct 17 $140,000 - $150,000 Norwalk, Connecticut, United States of America Apply →Principal CoreValve Therapy Development SpecialistApply →Fresh
Oct 17 $140,000 - $150,000
Norwalk, Connecticut, United States of AmericaWe are seeking a committed professional to join our team. While this is a remote position not located at a physical Medtronic site, the candidate hired will be required to reside within the territory and drive to multiple accounts throughout the region. A valid driver's license is essential for this role. The CoreValve Principal Therapy Development Specialist (TDS) provides technical, clinical, educational and sales support to ensure safe adoption and growth of the Medtronic CoreValve System and future catheter-based therapy technologies. The CoreValve Therapy Development Specialist works closely with implanting teams and the Medtronic Catheter-Based Therapies (CBT) and CVG... | |
CoreValve Therapy Development Specialist - Eugene, ORFresh
Oct 17 $110,000 - $115,000 Eugene, Oregon, United States of America Apply →CoreValve Therapy Development Specialist - Eugene, ORApply →Fresh
Oct 17 $110,000 - $115,000
Eugene, Oregon, United States of AmericaWe are seeking a committed professional to join our team. While this is a remote position not located at a physical Medtronic site, the candidate hired will be required to reside within the territory and drive to multiple accounts throughout the region. A valid driver's license is essential for this role. The CoreValve Therapy Development Specialist provides technical, clinical, educational and sales support to ensure safe adoption and growth of the Medtronic CoreValve System and future catheter-based therapy technologies. The CoreValve Therapy Development Specialist works closely with implanting teams and the Medtronic Catheter-based Therapies (CBT) and CVG field organizations... | |
Principal CoreValve Therapy Development Specialist - Los AngelesFresh
Oct 17 $140,000 - $150,000 Los Angeles, California, United States of America Apply →Principal CoreValve Therapy Development Specialist - Los AngelesApply →Fresh
Oct 17 $140,000 - $150,000
Los Angeles, California, United States of AmericaThe CoreValve Principal Therapy Development Specialist (TDS) provides technical, clinical, educational and sales support to ensure safe adoption and growth of the Medtronic CoreValve System and future catheter-based therapy technologies. The CoreValve Therapy Development Specialist works closely with implanting teams and the Medtronic Catheter-Based Therapies (CBT) and CVG field organizations to drive procedural and practice success. Technical and Clinical Expertise Provide clinical expertise for TAVR implanting centers, including “scrubbing in” for TAVI implant procedures to assist with loading valves onto delivery catheter, and providing technical support in accordance with the instructions for use/trial protocol, and best -practices to facilitate procedural... | |
Director, Clinical Research, Cardiovascular and RespiratoryFresh
Oct 17 $250,800 - $394,800 USA - New Jersey - Rahway Apply →Director, Clinical Research, Cardiovascular and RespiratoryApply →Fresh
Oct 17 $250,800 - $394,800
USA - New Jersey - RahwayOur Clinical Research team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine. Summary, Focus and Purpose The Cardiovascular and Respiratory Clinical Research Director has primary responsibility for planning and directing clinical research activities involving new or marketed cardiovascular and respiratory medicines. Our Company's cardiovascular and respiratory medicines span all phases of clinical development (pre-clinical to post-licensure). The Director will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and... | |
Principal Scientist, Clinical Trial Biomarkers/Clinical GenomicsFresh
Oct 17 $153,800 - $242,200 USA - New Jersey - Rahway Apply →Principal Scientist, Clinical Trial Biomarkers/Clinical GenomicsApply →Fresh
Oct 17 $153,800 - $242,200
USA - New Jersey - RahwayTranslational Molecular Biomarkers (TMB) is responsible for translating preclinical molecular biomarkers into clinical development across all therapeutic areas and all phases of clinical development at our Research & Development Division . TMB laboratories leverage a diverse array of technologies to develop biomarker assays to help confirm engagement of therapeutic targets and understand mechanisms of drug action and patient response. The Genomics group within TMB is seeking a highly motivated and skilled candidate for a Principal Scientist position. This role is essential for developing, optimizing, and deploying biomarker assays to enable clinical development at our Company. Key responsibilities Serve as a... | |
Associate Director, Clinical Research Lead - Cardiometabolic Health (Texas, Georgia, Alabama, South Carolina)Fresh
Remote
Oct 16 $111,000 - $195,800 US, Remote Apply →Associate Director, Clinical Research Lead - Cardiometabolic Health (Texas, Georgia, Alabama, South Carolina)Apply →Fresh
Remote
Oct 16 $111,000 - $195,800
US, RemoteAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Purpose The Clinical Research Lead (CRL) is a strategic, field-based scientific... | |
Clinical Research Associate llFresh
Oct 16 $79,500 - $138,700 United States - California - Alameda Apply →Clinical Research Associate llApply →Fresh
Oct 16 $79,500 - $138,700
United States - California - AlamedaClinical Research Associate II The Clinical Research Associate II will assist in the clinical execution and management of all aspects of assigned clinical studies. This includes but not limited to planning and implementation of clinical studies from concept to clinical study report per timelines and quality standards. This position will be based out of our Abbott Diabetes Care in Alameda, CA and the individual will be expected to be onsite Monday-Friday. What You’ll Work On The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Conduct... | |
Senior Field Clinical Research Specialist - RDNFresh
Oct 15 $108,000 - $162,000 Denver, Colorado, United States of America Apply →Senior Field Clinical Research Specialist - RDNApply →Fresh
Oct 15 $108,000 - $162,000
Denver, Colorado, United States of AmericaTogether, we can change healthcare worldwide. You will be responsible for clinical trial site management, case coverage, and clinical trial data tracking. This is field based, customer – facing position. You will be the “front line” of Medtronic clinical study conduct at the site level, forming customer relationships that will ensure studies are conducted effectively and efficiently, in accordance with applicable laws and regulations. Responsibilities Responsibilities may include the following and other duties may be assigned. Provides field support for various clinical research studies by selecting sites, performing activation duties, setting up protocols, providing training, helping to enroll participants,... | |
Clinical Research Associate ll - Oncology (Remote - Oregon)Fresh
Remote
Oct 15 $82,500 - $157,500 Oregon City, OR, United States Apply →Clinical Research Associate ll - Oncology (Remote - Oregon)Apply →Fresh
Remote
Oct 15 $82,500 - $157,500
Oregon City, OR, United StatesThe CRA II advances AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for patients, and leveraging advanced capabilities to drive industry-leading performance. The CRA II partners with investigators and site staff to build meaningful, effective engagements that position AbbVie as the sponsor of choice in clinical trials. The role focuses on site clinical research by ensuring proper trial conduct, while continually working to improve data integrity, compliance, overall study performance, and the customer experience. Responsibilities Considered as the primary point of contact for the investigative site. High level of competency or experience in providing contextual... | |
POSITION SUMMARY Assists in analyzing specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES Assist in testing of patient samples according to standard operating procedure. Meet expected performance metrics within role as applicable. Responsible for maintaining updated understanding and knowledge of methods performed in the lab Provide guidance for new team members. Follows GLP (good laboratory practice) maintain clean and organized workspace Completes training and other deadlines on time. Recognizes, escalates, and troubleshoot equipment malfunctions and common processing errors according to the laboratory’s standard operating procedures Recognizes, documents, and escalates... | |
Clinical Lab Assoc III, Pre-AnalyticalFresh
Oct 15 $37,000 - $63,000 US - WI - Madison Apply →Clinical Lab Assoc III, Pre-AnalyticalApply →Fresh
Oct 15 $37,000 - $63,000
US - WI - MadisonHelp us change lives At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others. Position Overview The Clinical Lab Assoc III, Pre-Analytical is responsible for performing the day-to-day operations of the Specimen Processing Department; including, but not limited to, lab productivity and process line support, exception handling, lab maintenance, and lab logistics. Tasks may... | |
Clinical Research SpecialistFresh
Oct 15 $83,200 - $124,800 Minneapolis, Minnesota, United States of America Apply →Clinical Research SpecialistApply →Fresh
Oct 15 $83,200 - $124,800
Minneapolis, Minnesota, United States of AmericaIn this exciting role as a Clinical Research Specialist, you will have primary focus responsibility in preparing sites for data collection, relationship building with research coordinators, regulatory report writing, and data cleaning. The CRS works under the direction of a Clinical Study Manager and assists with numerous tasks associated with the execution of a clinical trial. The Study & Scientific Solutions (S&SS) is a function within Medtronic Core Clinical Solutions (MC2). S&SS is an internal service provider to all of Medtronic and assigns resources to assist Business Units execute on clinical trials and scientific projects when they have an increase... | |
Clinical Associate Our Abbott story is one of delivering bold solutions in the face of complex healthcare challenges. At Abbott Electrophysiology (EP), we’ve been a leader for over 20 years, pioneering one of the first mapping systems, introducing the first contact force ablation catheter and creating a portfolio of products trusted in millions of procedures around the world. We have and will continue to redefine what’s possible in an evolving and challenging EP landscape. When you join Abbott EP, you become part of a passionate group of individuals who are dedicated to driving the EP space forward and... | |
Director, Trial Management, Medical Affairs Delivery UnitOct 14 $160,000 - $276,000 Raritan, New Jersey, United States of America Apply →Director, Trial Management, Medical Affairs Delivery UnitApply →Oct 14 $160,000 - $276,000
Raritan, New Jersey, United States of AmericaAbout Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing... | |
Clinical Research Associate ll - Oncology (Remote - Nebraska)Remote
Oct 14 $82,500 - $157,500 Lincoln, NE, United States Apply →Clinical Research Associate ll - Oncology (Remote - Nebraska)Apply →Remote
Oct 14 $82,500 - $157,500
Lincoln, NE, United StatesThe CRA II advances AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for patients, and leveraging advanced capabilities to drive industry-leading performance. The CRA II partners with investigators and site staff to build meaningful, effective engagements that position AbbVie as the sponsor of choice in clinical trials. The role focuses on site clinical research by ensuring proper trial conduct, while continually working to improve data integrity, compliance, overall study performance, and the customer experience. Responsibilities Considered as the primary point of contact for the investigative site. High level of competency or experience in providing contextual... | |
Clinical Research Associate ll - Oncology (Remote - Philadelphia)Remote
Oct 14 $82,500 - $157,500 Philadelphia, PA, United States Apply →Clinical Research Associate ll - Oncology (Remote - Philadelphia)Apply →Remote
Oct 14 $82,500 - $157,500
Philadelphia, PA, United StatesThe CRA II advances AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for patients, and leveraging advanced capabilities to drive industry-leading performance. The CRA II partners with investigators and site staff to build meaningful, effective engagements that position AbbVie as the sponsor of choice in clinical trials. The role focuses on site clinical research by ensuring proper trial conduct, while continually working to improve data integrity, compliance, overall study performance, and the customer experience. Responsibilities Considered as the primary point of contact for the investigative site. High level of competency or experience in providing contextual... | |
POSITION SUMMARY Natera is currently seeking a Clinical Laboratory Associate to analyze laboratory specimens following the standard methods and procedures while maintaining equipment and instruments in good operating condition by troubleshooting malfunctions as needed. PRIMARY RESPONSIBILITIES Assists in testing of patient samples according to standard operating procedure in an efficient manner with little to no errors Responsible for maintaining updated understanding and knowledge of methods performed in the lab Follows GLP (good laboratory practice) maintain cleans and organized work space Completes training and other deadlines on time. Recognizes and escalates equipment malfunctions; troubleshoots common errors on the lab floor Recognizes,... | |
Senior Director, Clinical Research, AtherosclerosisOct 14 $276,600 - $435,400 USA - New Jersey - Rahway Apply →Senior Director, Clinical Research, AtherosclerosisApply →Oct 14 $276,600 - $435,400
USA - New Jersey - RahwayThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical development and studies, including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. Specifically, the Senior Director May Be Responsible For Evaluating pre-clinical and translational work for the purpose of generating early clinical development plans and Investigational New... | |
VP Clinical Development, Clinical Research Head HepatologyOct 14 Salary N/A USA - Massachusetts - Waltham Apply →VP Clinical Development, Clinical Research Head HepatologyApply →Oct 14 Salary N/A
USA - Massachusetts - WalthamCLOSING DATE Tuesday 28th October 2025 Are you an exceptional clinical development leader in Hepatology, driven to advance cutting-edge science and deliver impactful medicines to patients? If so, this VP Clinical Development, Clinical Research Head Hepatology position offers a unique opportunity to lead and innovate within GSK’s advanced portfolio. GSK seeks an outstanding leader in clinical development to join as VP Clinical Development, Clinical Research Head Hepatology within the Advanced Portfolio. The Advanced Portfolio Unit works within the Respiratory, Immunology and Inflammation Research Unit (RIIRU). This represents a critical and senior role at GSK, with an opportunity to provide leadership... | |
International Logistics Coordinator - Nutrition- Columbus, OHOct 14 $24 - $49 United States - Ohio - Columbus Apply →International Logistics Coordinator - Nutrition- Columbus, OHApply →Oct 14 $24 - $49
United States - Ohio - ColumbusInternational Logistics Coordinator This position works out of our Columbus, OH location in the Nutrition Division . Provides focused expertise within a specific area in Export Logistics, or coordinates, in a lead capacity, a specific area of operations. WHAT YOU’LL DO Main Responsibilities Works with exports team and carrier to comply with all U.S. export regulations Works with affiliate and direct export customers so that all documentation is in accordance with countries import customs and regulations Perform all aspects of order process (such as order execution, invoicing, post shipment, etc.) Support Exports customs clearance and documentation Specific Functional responsibilities... | |
Senior Principal Scientist, Clinical Research, NeuroscienceOct 13 $276,600 - $435,400 USA - New Jersey - Rahway Apply →Senior Principal Scientist, Clinical Research, NeuroscienceApply →Oct 13 $276,600 - $435,400
USA - New Jersey - RahwayOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards. The Senior Director (Senior Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Neuroscience Medicines. Our company's Neuroscience Medicines span all phases of clinical development (pre-clinical to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical... | |
Help us change lives At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others. Position Overview The Workflow Coordinator (Wed - Sat 1100am - 930pm) manages the entire workflow of patient samples to ensure quality and turnaround times are met. This will include close partnership with laboratory staff and various functions on sample processing... | |
Clinical Associate Our Abbott story is one of delivering bold solutions in the face of complex healthcare challenges. At Abbott Electrophysiology (EP), we’ve been a leader for over 20 years, pioneering one of the first mapping systems, introducing the first contact force ablation catheter and creating a portfolio of products trusted in millions of procedures around the world. We have and will continue to redefine what’s possible in an evolving and challenging EP landscape. When you join Abbott EP, you become part of a passionate group of individuals who are dedicated to driving the EP space forward and... | |
POSITION SUMMARY Assists in analyzing specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES Assist in testing of patient samples according to standard operating procedure. Meet expected performance metrics within role as applicable. Responsible for maintaining updated understanding and knowledge of methods performed in the lab Provide guidance for new team members. Follows GLP (good laboratory practice) maintain clean and organized workspace Completes training and other deadlines on time. Recognizes, escalates, and troubleshoot equipment malfunctions and common processing errors according to the laboratory’s standard operating procedures Recognizes, documents, and escalates protocol... | |
Clinical Lab Associate I, Specimen Processing Tuesday-Friday 6am-4:30pmOct 13 $34,000 - $54,000 US - WI - Madison Apply →Clinical Lab Associate I, Specimen Processing Tuesday-Friday 6am-4:30pmApply →Oct 13 $34,000 - $54,000
US - WI - MadisonHelp us change lives At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others. Position Overview The Clinical Lab Associate I, Specimen Processing is responsible for performing the day-to-day operations of the Specimen Processing Department including, but not limited to, lab productivity and process line support, such as accessioning, processing, automation usage, sample racking,... | |
Senior Principal Scientist, Clinical Research, ImmunologyOct 13 $276,600 - $435,400 USA - New Jersey - Rahway Apply →Senior Principal Scientist, Clinical Research, ImmunologyApply →Oct 13 $276,600 - $435,400
USA - New Jersey - RahwayThe Senior Director (Sr. Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical development, including determination of appropriate disease indications to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. Specifically, The Senior Director May Be Responsible For Evaluating pre-clinical and translational work for the purpose of generating the early clinical development plan and Investigational New Drug applications. Providing clinical development support of business development assessments of external opportunities... | |
Clinical Associate Our Abbott story is one of delivering bold solutions in the face of complex healthcare challenges. At Abbott Electrophysiology (EP), we’ve been a leader for over 20 years, pioneering one of the first mapping systems, introducing the first contact force ablation catheter and creating a portfolio of products trusted in millions of procedures around the world. We have and will continue to redefine what’s possible in an evolving and challenging EP landscape. When you join Abbott EP, you become part of a passionate group of individuals who are dedicated to driving the EP space forward and... | |
Clinical Associate Our Abbott story is one of delivering bold solutions in the face of complex healthcare challenges. At Abbott Electrophysiology (EP), we’ve been a leader for over 20 years, pioneering one of the first mapping systems, introducing the first contact force ablation catheter and creating a portfolio of products trusted in millions of procedures around the world. We have and will continue to redefine what’s possible in an evolving and challenging EP landscape. When you join Abbott EP, you become part of a passionate group of individuals who are dedicated to driving the EP space forward and... | |
Project Coordinator IIIOct 13 $54,400 - $81,600 Mounds View, Minnesota, United States of America Apply →Project Coordinator IIIApply →Oct 13 $54,400 - $81,600
Mounds View, Minnesota, United States of AmericaWe are excited to be hiring a Clinical Studies Project Coordinator III to join our Medtronic Structural Heart and Aortic (SH&A) Operating Unit. In this role, you will be providing support to the Mitral and Tricuspid (M&T) clinical teams and studies. The Clinical Studies Project Coordinator III will independently perform diverse administrative and project duties. The Structural Heart and Aortic integrated operating unit offers minimally invasive approaches to restore proper structure and function of the heart and the aorta. We focus on the transcatheter replacement or repair of the four heart valves—aortic, pulmonic, mitral, tricuspid—and the placement of stent grafts... | |
Project Coordinator IVOct 13 $62,400 - $93,600 Fridley, Minnesota, United States of America Apply →Project Coordinator IVApply →Oct 13 $62,400 - $93,600
Fridley, Minnesota, United States of AmericaUse your passion, organizational skills, and proactive nature to support leaders within our Operations Innovation group. Your skills and positive attitude will be essential to help accelerate our ability to meet our goals and delight our business partners. If you have strong communication skills and are highly organized with an ability to prioritize, this winning team would love to have you join them! The position’s primary focus is to provide elevated project and program support to the Operations Innovation team as well as expert executive-level administrative support to the leader of the Operations Innovation team. In this role, you will... | |
POSITION SUMMARY The Natera Test Coordinator plays a vital role in ensuring a seamless testing experience for patients. This position is responsible for scheduling and determining the most effective method for blood collection, preparing specimens for laboratory testing, and managing all necessary paperwork to ensure compliance. In this role, you will work closely with customers and the sales team to facilitate an efficient ordering process and timely reporting of results. The ideal candidate thrives in an independent work environment, excels at multitasking, and demonstrates strong critical thinking skills to resolve issues promptly. *This is an onsite position in Carmel,... | |
POSITION SUMMARY The Natera Test Coordinator plays a vital role in ensuring a seamless testing experience for patients. This position is responsible for scheduling and determining the most effective method for blood collection, preparing specimens for laboratory testing, and managing all necessary paperwork to ensure compliance. In this role, you will work closely with customers and the sales team to facilitate an efficient ordering process and timely reporting of results. The ideal candidate thrives in an independent work environment, excels at multitasking, and demonstrates strong critical thinking skills to resolve issues promptly. *This is an onsite position in Houston,... | |
Purpose Responsible for day to day inbound, outbound and third party domestic shipment requests. Accountable for the settings within SAP which control the selection of the carrier for shipments from the AbbVie DCs located in Lake County, IL. The Coordinator will work with the carriers to ensure established turn by turn directions are established for outbound truckload shipments are out of the AbbVie Lake County DC. This individual will use systems to plan and communicate bookings each week, and will keep the stakeholders informed of last minute changes. As the main interface on day to day bookings, this individual will... | |
Coordinator, Regulatory Affairs US Advertising and Promotion (Office-based)Oct 9 $58,656 - $100,500 Mettawa, IL, United States Apply →Coordinator, Regulatory Affairs US Advertising and Promotion (Office-based)Apply →Oct 9 $58,656 - $100,500
Mettawa, IL, United StatesThe US Advertising and Promotion Coordinator combines knowledge of the pharmaceutical business landscape to drive the aims and purpose of the U.S. Advertising and Promotion (USAP) department including the Regulatory review of non-promotional materials, providing operational guidance and development of USAP metrics and trends, as well as, creation and maintenance of sharepoint sites and other business platforms. The contribution from this role will directly benefit the USAP area, as well as cross-functional stakeholders including U.S. Commercial and Research and Development areas Global Medical Affairs, Clinical, and HEOR. Responsibilities Functions independently in evaluation and negotiation of R&D (MedComms) project related topics... | |
POSITION SUMMARY Temp to Perm position located in Las Vegas, NV The Natera Test Coordinator plays a vital role in ensuring a seamless testing experience for patients. This position is responsible for scheduling and determining the most effective method for blood collection, preparing specimens for laboratory testing, and managing all necessary paperwork to ensure compliance. In this role, you will work closely with customers and the sales team to facilitate an efficient ordering process and timely reporting of results. The ideal candidate thrives in an independent work environment, excels at multitasking, and demonstrates strong critical thinking skills to resolve issues... | |
The Clinical Trial Manager (CTM) is accountable for end-to-end study operational oversight and delivery at country level, ensuring adherence to timelines, budget and quality standards. Acts as the primary point of contact at a country level for both internal and external stakeholders, ensuring clear communication, effective coordination, and successful project execution. Key Responsibilities Acts as the main point of contact for a country with global study team members and accountable for the coordination with local country cross functional teams. Implements the local country and site feasibility process, including proposal and validation of country study targets, as endorsed by country leadership.... | |
Lead Professional Education CoordinatorOct 9 $28 - $43 USA - GA - Social Circle - Hwy 278 Apply →Lead Professional Education CoordinatorApply →Oct 9 $28 - $43
USA - GA - Social Circle - Hwy 278About the Role The Manufacturing Trainer position is responsible for developing trainees into qualified associates following company procedures. The trainer role will execute production activities in addition to other facility production training support, as needed. This position has sufficient technical and administrative competence to organize and lead production activities, including demonstrating leadership in state-of-the-art cGMP compliance, and environmental health and safety skills. How you will contribute Provide on the job training and assisting with e-learning requirements. Analyze training needs, monitor training compliance Provide constructive feedback and coaching to associates. Perform hands-on execution of manufacturing operations to support production schedule as... | |
Clinical Lab Associate I, Pre-Analytical - Tuesday-Friday 12:30pm-11:00pmOct 9 $31,000 - $52,000 US - WI - Madison Apply →Clinical Lab Associate I, Pre-Analytical - Tuesday-Friday 12:30pm-11:00pmApply →Oct 9 $31,000 - $52,000
US - WI - MadisonHelp us change lives At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others. Position Overview The Clinical Lab Associate I, Specimen Processing is responsible for performing the day-to-day operations of the Specimen Processing Department including, but not limited to, lab productivity and process line support, such as accessioning, processing, automation usage, sample racking,... | |
Associate Principal Scientist, Clinical Research (Animal Health)Oct 8 $139,600 - $219,700 USA - New Jersey - Rahway Apply →Associate Principal Scientist, Clinical Research (Animal Health)Apply →Oct 8 $139,600 - $219,700
USA - New Jersey - RahwayPrimary activities include but are not limited to The Associate Principal Scientist is a DVM and/or PhD whose primary function is to design, coordinate, monitor, and report clinical laboratory and field studies that will support the regulatory approval of new companion animal and livestock products. The position requires the candidate be responsible for the conduct of Good Clinical Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study team leader and has overall responsibility for a study. The Associate Principal Scientist can also be responsible for several effectiveness studies within a... | |
Clinical Associate Our Abbott story is one of delivering bold solutions in the face of complex healthcare challenges. At Abbott Electrophysiology (EP), we’ve been a leader for over 20 years, pioneering one of the first mapping systems, introducing the first contact force ablation catheter and creating a portfolio of products trusted in millions of procedures around the world. We have and will continue to redefine what’s possible in an evolving and challenging EP landscape. When you join Abbott EP, you become part of a passionate group of individuals who are dedicated to driving the EP space forward and... | |
Summer 2026 - Undergraduate Precision Medicine, BioAnalytical and Translational Sciences InternshipOct 8 $27 - $29 Princeton - NJ - US Apply →Summer 2026 - Undergraduate Precision Medicine, BioAnalytical and Translational Sciences InternshipApply →Oct 8 $27 - $29
Princeton - NJ - USPrecision Medicine, BioAnalytical, and Translational Sciences (PMBATS) has multiple internships for qualified candidates to work alongside PMBATS teams by contributing to development and execution of biomarker/BA process, laboratory experiments, enable our mission of providing technology solutions for BMS development assets. We have opportunities in Translational Pathology and Immunohistochemistry (TP-IHC) team seeks a motivated, inquisitive intern to join a collaborative team translating tissue-based data into clinical insights that guide delivery of therapies to patients most likely to benefit. You will support biomarker discovery and translational research through assay development, image analysis, and supervised experimentation using cutting-edge technologies, while learning in a... | |
Sr. Inventory Coordinator -Based in PittsburghOct 8 $83,200 - $124,800 Pittsburgh, Pennsylvania, United States of America Apply →Sr. Inventory Coordinator -Based in PittsburghApply →Oct 8 $83,200 - $124,800
Pittsburgh, Pennsylvania, United States of AmericaCareers that Change Lives The Sr. Inventory Coordinator role is an on-site/office position that is responsible for managing the Spinal inventory dedicated to the specified sales area. This position will be responsible for tracking inventory and logistically securing the inventory for spine cases at hospitals and surgery centers in the local area surrounding the office. The Sr. Inventory Coordinator works closely with local sales managers and sales reps in managing the assigned inventory and ensuring top utilization of the systems. This role acts as an “air traffic controller”, dictating where the inventory needs to be going, utilizing local Medtronic drivers,... | |
Associate Clinical Research Medical Director CRMRemote
Oct 7 $204,400 - $379,600 Remote Position (USA) Apply →Associate Clinical Research Medical Director CRMApply →Remote
Oct 7 $204,400 - $379,600
Remote Position (USA)Accountable for all country clinical/medical aspects associated with Development and prioritized research programs/trials by providing clinical strategic and tactical leadership as the Country Clinical Development representative. Gathers, informs, and acts on clinical/medical/scientific insights for clinical trial concept sheets/protocols, Informed Consent Forms (ICFs) and other relevant clinical documents to optimize clinical trial implementation. Drives the identification and involvement of qualified investigators with greatest recruitment potential, identifies clinical recruitment hurdles and drives clinical recruitment activities to overcome these hurdles. Accountable for adherence to safety standards and clinical data quality in the country by providing general clinical/medical support for trial... | |
Director, Clinical Trial MaterialsOct 7 $177,000 - $221,700 Princeton, New Jersey, United States; San Diego, California, United States Apply →Director, Clinical Trial MaterialsApply →Oct 7 $177,000 - $221,700
Princeton, New Jersey, United States; San Diego, California, United StatesIn support of clinical development programs, the Director of Clinical Trial Materials role supports the Sr. Director Clinical Trial Material (CTM) in planning and execution activities, supporting Phase 1-IV and IIS trials. Includes defining short and long term goals for the Team, demand forecasting and budget management, setting production schedules, protocol review, ensures label development and works cross functionally to align compliance with applicable regulations, establishes optimal packaging & distribution strategies, tracks and reconciles drug supplies and monitors product re-test dates. Interface with internal departments and contract research organizations (CROs) and Contract Manufacturing Organizations (CMOs) as necessary to coordinate the... | |
POSITION SUMMARY This is a temporary position for 6 months located in Austin, TX. ** Available Shift Schedules 6 am - 230 pm OR 2 pm - 1030 pm (with 10% shift differential). Assists in analyzing specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES Assist in testing of patient samples according to standard operating procedure. Meet expected performance metrics within role as applicable. Responsible for maintaining updated understanding and knowledge of methods performed in the lab Provide guidance for new team members. Follows GLP (good laboratory practice) maintain clean and... | |
Associate Director, Above Brand & Digital Lead, US Precision MedicineOct 7 $180,875 - $271,312 US - Gaithersburg - MD Apply →Associate Director, Above Brand & Digital Lead, US Precision MedicineApply →Oct 7 $180,875 - $271,312
US - Gaithersburg - MDAssociate Director, Above Brand & Digital Lead, US Precision Medicine Are you ready to make a significant impact in the world of precision medicine? As the Associate Director, Above Brand & Digital Lead for Precision Medicine Marketing, you'll be at the forefront of shaping the commercialization of AstraZeneca’s precision-enabled therapies. Your mission? To design and implement a robust above brand strategy with a focus on digital and non-personal promotion execution. Collaborate with Precision Medicine Marketing Indication Leads and take ownership of above brand content and deployment. This exciting role is based at our Gaithersburg, MD campus, the hub for US... | |
Senior Clinical Trial SpecialistOct 7 $105,000 - $169,050; $121,000 - $194,350 Cincinnati, Ohio, United States of America Apply →Senior Clinical Trial SpecialistApply →Oct 7 $105,000 - $169,050; $121,000 - $194,350
Cincinnati, Ohio, United States of AmericaAbout MedTech Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at Clinical Affairs of Robotics and Digital Solutions, Johnson & Johnson MedTech, is recruiting a Senior Clinical Trial Specialist. This role is responsible for managing all operational activities of assigned clinical trials well as fostering strong, productive relationships with colleagues across the organization. The Senior Clinical Trial Specialist ensures inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOPs),... | |
The AbbVie EXCEL Externship is a two-day, unpaid, immersive experience for 2nd year undergraduate (sophomore) students interested in future internships with AbbVie. Students will join us at AbbVie's Headquarters in Lake County, IL during August 2026 to Get immersed in AbbVie’s culture Gain hands-on experience in a variety of key business areas Build an extended network of AbbVie representatives, senior leaders, and students from across the country Participate in cross-functional professional development opportunities Learn more about AbbVie’s career opportunities Be considered for an internship for the following summer AbbVie will provide travel, transportation, and lodging for eligible students. Clinical Trial... | |
Manager, Trial Master File (TMF) OperationsOct 6 $122,000 - $133,000 Millbrae, CA; Jersey City, NJ Apply →Manager, Trial Master File (TMF) OperationsApply →Oct 6 $122,000 - $133,000
Millbrae, CA; Jersey City, NJPosition The Manager, TMF Operations role ensures a complete, accurate and high-quality Trial Master File (TMF) as the subject matter expert through proper, consistent documentation and proactive partner relationship with the clinical study teams. This role will work directly with all functions (internal and external) who contribute to the TMF to ensure regulatory inspection readiness for clinical trials. In addition to ensuring TMF Quality, this role will assist in TMF set-up, document collection and filing, monitoring quality, timeliness, and completeness, and following-up with study teams to resolve TMF-related issues. This role will require a minimum of 3 days a week... | |
The Environmental Health & Safety (EHS) Coordinator supports day-to-day safety operations and helps maintain compliance with company policies and applicable regulations. This entry-level role works closely with Lab Operations, Research & Development, Facilities, and Quality Assurance teams to promote a safe and healthy workplace. The coordinator will gain hands-on experience in EHS program support and will assist senior EHS staff in ensuring workplace safety and environmental compliance. · Assist with day-to-day safety operations, including · Helping deliver or coordinate safety training for employees. · Supporting compliance with safety policies and regulatory requirements. · Assisting with... | |
Help us change lives At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others. Position Overview The Sr Clinical Lab Quality Data Engineer plays a critical role in ensuring accuracy, consistency, and integrity of laboratory data with a strong focus on molecular and next-generation sequencing (NGS) quality control processes. This role integrates advanced data... | |
Senior Clinical Research Scientist (Irvine, CA) Johnson and Johnson, MedTech ElectrophysiologyOct 6 $89,000 - $143,750 Irvine, California, United States of America Apply →Senior Clinical Research Scientist (Irvine, CA) Johnson and Johnson, MedTech ElectrophysiologyApply →Oct 6 $89,000 - $143,750
Irvine, California, United States of AmericaJohnson and Johnson is currently seeking a Senior Clinical Research Scientist to support the real-world evidence and evidence generation strategy needs of the Electrophysiology business. This role is based in Irvine, CA and reports to the office on assigned days 2-3 times per week. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full... |