Clinical Operations Jobs in Pharma & Biotech

About the job Your skills could be critical in helping our teams accelerate progress. Join our Fitusiran Clinical Team as Senior Clinical Research Director and you will be the primary Clinical Lead for Phase 3 registrational studies and on-going NDA submissions. Qfitlia (fitusiran) is a first-in-class AT lowering therapy approved by the US FDA for prophylactic treatment of adults and pediatric patients We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&D to sales, our talented teams work together, revolutionizing treatment,...

Twist Bioscience is looking for an individual that is highly motivated, collaborative, takes pride in their work, and great attention to detail. This position will play a critical role in forming a best in class Shipping/Order Fulfillment team. This position will require interactions with Manufacturing, Customer Support, Receiving, Warehouse, and Supply Chain teams to ensure internal and external customer satisfaction while ensuring all orders are processed and shipped in a timely and required manner. The Shipping Coordinator II will perform all administrative and physical requirements of this position. What You’ll Be Doing ●Pick & Pull products in accordance to the...

Per Template 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 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...

POSITION SUMMARY The Logistics Coordinator will support operational activities related to the inbound and outbound transport of biological specimens and collection kit manufactured products. Responsibilities will include tracking specimens from the point of pickup through delivery. Employees will act as a liaison between Customer and both external and internal partners. Job assignments should be managed without immediate supervision and evaluated based on performance. Individuals must be able to perform each essential core function as well as monitor and maintain the department service levels. All work is subject to additional requests as assigned by Department Manager. Coordinates and consolidates domestic...

POSITION SUMMARY The role of Patient Coordinator will be central to the success of the Prospera product line. This position will be focused on growing the relationship between Natera and its patients to ensure timely management of testing. Core responsibilities include collaborating with Nurse Coordinators to increase revenue and drive market development through direct sales by being the key contact for patient needs. The Patient Coordinator will accomplish this by being the patient advocate within Natera. *Spanish strongly preferred* PRIMARY RESPONSIBILITIES Work with assigned Nurse Coordinator to maintain & support existing customers. Assess the needs of patients with a...

Clinical Associate In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. What You’ll Work On Working under general direction, provides engineering, sales, educational and technical support in response to field inquiries from physicians, health care professionals, patients, and field sales staff, involving EP products. Performs work that involves a high degree of independence. Identifies and routinely uses the most effective, cost efficient and best business practices to execute processes; continually evaluates their effectiveness and appropriateness. Exercises...

Prin Clinical Research Spec – Surgical Robotics Operating Unit The Principal Clinical Research Spec is responsible for developing strategies and driving processes to meet the milestones of complex clinical studies/projects in compliance with applicable clinical and regulatory standards and in alignment with Medtronic business needs. This role utilizes their broad range of experience in managing the technical execution of the trial and manages trials of a higher degree of complexity and global nature. This role works independently and under only general direction. Major deliverables are reviewed to ensure clinical and business requirements are met. The position provides work direction and...

The Sr. Clinical Director for Neuromodulation, Pain Therapies reports to the VP, Clinical Research and Medical Science NMPH. This position is responsible for directing all global clinical research activities and programs to generate clinical evidence in support of the business. The Sr. Clinical Director is responsible for supporting the clinical strategy in alignment with the business, R&D, regulatory and commercial strategies for the pain therapies business. The leader is also responsible for designing and driving the execution of pre-market and post-market clinical trials globally, including driving outcomes and results, and collaborating for the dissemination of the resulting evidence to internal...

Location Remote position within the United States Travel up to 25% (domestic and may include international travel). In this exciting role as a Clinical Research Manager (CRM) , you will have primary focus responsibility to oversee all clinical activities related to one or more clinical studies and performing/directing/managing the daily in-house activities associated with the studies. This is a people leadership role. The CRM will report to the US Sr. Clinical Research Manager and independently handle various clinical study assignments, have management responsibility, and oversees and directs the work of a team of Clinical Research Specialists at all levels, from...

Make a difference in patients' lives by applying your diagnostic and clinical test market expertise as a Precision Medicine Liaison! Key responsibilities include ensuring the timely, high quality in-market companion diagnostics / testing solutions are available to support optimal treatment. Engage collaborators before and after launch to provide approved information to proactively address barriers to testing at pre-specified region reference labs, pathology medical groups and a subset of academic/health system with well-developed diagnostic and molecular capabilities within assigned geography. Act as the regional expert to support oncology customers at the request of the cross functional team by providing more in-depth...

Accelerating the execution of our priority clinical trials is an imperative and a critical enabler of our Drug Development strategy to launch 10 new treatments in 30 new indications by 2030. At the center of our acceleration efforts is methodology and ability to assemble wide-ranging data - structured, tactical and ad hoc - into timely insights which then support precision actions. The Executive Director, Trial Analytics , Insights and Planning (TAIP) is accountable for driving end-to-end analytics excellence within Global Development Operations (GDO) and is a key function within the Trial Delivery Support team. In this steady-state model, the Executive...

POSITION SUMMARY The Logistics Coordinator will support operational activities related to the inbound and outbound transport of biological specimens and collection kit manufactured products. Responsibilities will include tracking specimens from the point of pickup through delivery. Employees will act as a liaison between Customer and both external and internal partners. Job assignments should be managed without immediate supervision and evaluated based on performance. Individuals must be able to perform each essential core function as well as monitor and maintain the department service levels. All work is subject to additional requests as assigned by Department Manager. Coordinates and consolidates domestic...

Johnson & Johnson is hiring for a Clinical Research Associate II - Shockwave Reducer (Remote) to join our team. The position is FULLY REMOTE and can sit anywhere in the US. 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 spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly...

In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. What You’ll Work On Working under general direction, provides engineering, sales, educational and technical support in response to field inquiries from physicians, health care professionals, patients, and field sales staff, involving EP products. Performs work that involves a high degree of independence. Identifies and routinely uses the most effective, cost efficient and best business practices to execute processes; continually evaluates their effectiveness and appropriateness. Exercises independent judgment in planning,...

Clinical Associate In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. What You’ll Work On Working under general direction, provides engineering, sales, educational and technical support in response to field inquiries from physicians, health care professionals, patients, and field sales staff, involving EP products. Performs work that involves a high degree of independence. Identifies and routinely uses the most effective, cost efficient and best business practices to execute processes; continually evaluates their effectiveness and appropriateness. Exercises...

Clinical Associate In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. What You’ll Work On Working under general direction, provides engineering, sales, educational and technical support in response to field inquiries from physicians, health care professionals, patients, and field sales staff, involving EP products. Performs work that involves a high degree of independence. Identifies and routinely uses the most effective, cost efficient and best business practices to execute processes; continually evaluates their effectiveness and appropriateness. Exercises...

Clinical Research Associate (CRA), Oncology, As a Field Based Clinical Research Associate , you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. In this role as an Oncology CRA , you will have the local responsibility for the delivery of the studies at allocated centers and are active participants in the local study team(s). You’ll work in close collaboration with other Monitors and the Local Study Delivery Team to ensure that quality and quantity commitments are achieved in a timely and efficient manner. You will also be responsible for...

ROLE SUMMARY Primary purpose is to serve as a Clinician for the Pneumococcal Vaccine Franchise to assist in the global clinical development of a Pneumococcal Conjugate vaccines. The team has responsibility for global clinical development and licensure of pneumococcal vaccines, including post licensure regulatory commitments. This role will serve as a clinical lead for one or more studies, within a clinical program, and work closely with the clinical program lead who is ultimately responsible for execution of the overall program. Importantly, this role will lead a matrix team in executing studies and medical monitoring and take a lead in study...

We are devoted to discovering and developing new medicines for those patients with unmet medical needs. AbbVie's clinical research operates with a collaborative model that seeks to build the pipeline of discoveries from inside and outside the company's own walls. AbbVie's current therapeutic areas of interest are Antiviral (HCV, HIV and RSV), Immunology, Men's Health, Neuroscience, Oncology, Pain, Renal, and Women’s Health. Within each of these therapeutic areas, we have various products in development. The products will change over time as compounds progress through our development program. A critical component of medicinal product development is clinical research, which involves conducting...

PRIMARY RESPONSIBILITIES Review select cases for accuracy of tissue request and escalate to PA’s when needed, complete accurate data entry. Assist other PSCs in resolving issues with their cases and provide feedback on the quality of their work. Ensure that necessary notes and holds are placed on cases for non-conforming samples, discrepancies and/or missing information so that timely follow-up by the Customer Care team is made. Compose professional emails/faxes using proper grammar and spelling to communicate with other departments for case escalation and/or case status updates. Perform outbound calls to pathology labs for specimen information (confirmation of accession numbers, specimen...

The Executive Director, Head of Precision Medicine GU/GYN is accountable for driving and shaping the global Precision Medicine and Diagnostics Development Strategy for the tumour area. This includes guiding Precision Medicine and Companion Diagnostics plans, ensuring their alignment with the overall tumour strategy, and representing the Precision Medicine and Biosamples (PMB) function on the Tumour Council or strategy team. Key responsibilities include Providing strategic direction for Precision Medicine approaches and diagnostic development to the Tumour Councils and Therapeutic Area Leadership Team (TALT) and being the most senior point of reference for the PMB function in [tumour area] to governance, including...

At AstraZeneca we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. We're focused on the potential of science to address the unmet needs of patients around the world. We commit to those areas where we think we can really change the course of medicine and bring big new ideas to life. As a Precision Medicine Field Director (PMFD) you will provide inspirational leadership and prioritize to drive high performance through your regional Precision Medicine Manager team. As a role model, coach and a liaison you will...

Patent Coordinator - IP Litigation Administrative Coordinator What you will do In this vital role you will will provide administrative support to the Intellectual Property Litigation team. The successful candidate will provide support to the Intellectual Property Litigation team by assisting and supporting our litigation teams in the U.S. and global intellectual property litigations, including maintaining electronic databases. Candidate will also draft correspondence, e-mails, engagement letters with outside counsel; obtain references, case law, patents, file histories; organize materials, etc. The work assignments are sometimes complex in nature and require absolute discretion, as well as considerable tact, judgment, creativity, and...

We are searching for the best talent to join our Vision team as a Staff Clinical Research Scientist located in Jacksonville, FL Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges. Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for...

Translational Medicine is responsible for early clinical development of novel therapeutics, working in close collaboration with Discovery Sciences and late-stage Clinical Research across all therapeutic areas. Our team is focused on innovation and dedicated to translating breakthrough science into innovative medicines that extend and improve the lives of patients worldwide. Through clinical trials, we ensure the safety and efficacy of our pipeline and existing products to produce safe, effective, innovative medicine. The Early Clinical Scientist/ECS coordinates the design, planning and execution of early phase clinical trials with the Clinical Director and internal/external team members. Oversees trials within and/or across program(s)/therapeutic...

The Clinical Trial Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. Serves as a primary source of medical accountability and oversight for clinical trials Matrix management responsibilities across the internal and external network Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities Provides medical and scientific expertise to cross-functional BMS colleagues Medical Monitoring Contributes to and is a key member of a high performing Study Delivery Team (SDT) and may be a...

About Synchron Synchron is a clinical-stage endovascular brain computer interface (BCI) company. Since 2012, the company has been developing a BCI platform that avoids the need for open brain surgery by using a minimally-invasive procedure. The Synchron Switch ™ BCI received FDA Breakthrough Device Designation in 2020, and is currently in human clinical trials in the US and Australia. The company recently announced an oversubscribed $75 million Series C financing round led by ARCH Venture Partners, with participation from Gates Frontier, Bezos Expeditions and other top-tier investors. The funds will accelerate product development, facilitate commencement of a pivotal clinical...

Job Title Global Therapy Development Specialist We currently have an opportunity available for a Global Therapy Development Specialist to join our Vascular division. This is a fully Remote MAIN PURPOSE OF ROLE The Global Therapy Development Specialist champions issues that provide major implications for the company and may lead to accomplishing long-range objectives for US and OUS geographical areas. Provides broad, technical advice. Mentors sales trainers, marketing, and field sales personnel by sharing clinical and technical expertise and providing feedback and guidance. Acts as an advisor to management on specialized business projects (managerial, technical, leadership, clinical, training). Acts as...

Clinical Research Medical Director, Uplizna What you will do In this vital role you will serve as clinical expert to provide clinical/scientific knowledge into the development, delivery and communication of the global scientific/medical evidence plan for the indication(s). Provide oversight of LCM clinical development with input on global strategy Support cross-functional and global collaborations to integrate broad medical, regulatory, safety, scientific, and commercial access, and value input into the development program(s) Participate and provide clinical input into safety and regulatory interactions. Interpret and communicate clinical trial data. Author/review CSRs, publications, and regulatory submissions Develop key opinion leaders and make...

At 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. Through the application of scientific and medical training, clinical expertise, and...

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,...

This Director, Clinical Trial Physician (CTP), Oncology, Medical Evidence Generation (MEG) role in Medical Affairs manages set of studies within the evidence generation Oncology/Hematology portfolio (including Medical Affairs Sponsored studies [MAST], Clinical Research Collaborations (CRCs), and Investigator Sponsored Research (ISRs) – and provides clinical support for other studies in the MEG book of work (BOW). In this role, he/she will serve as the primary source of medical/clinical accountability and oversight for studies in alignment with the Integrated Evidence Plans (IEP) for specified assets. He/she will work closely with Worldwide Medical (WWM) Therapy Asset Lead, the MEG Oncology Lead, and other...

The Material Coordinator reports to the Supply Chain Operations Supervisor and/or Manager. Manages cold chain and patient material receipt, release, dispensing, inventory, and shipping for CAR-T production per Standard Operating Procedures (SOPs) in controlled and/or classified environments under the supervision of Supply Chain Operations Management. The position must adhere to regulatory requirements while performing job functions. Job duties are performed in alignment with CAR-T production schedules, may require weekend work. Communication and initiation of production deviations and assistance with quality investigations are required, as applicable. Key Responsibilities Records patient material handling / operations data and information in a clear, concise,...

The Director (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 Director will manage the entire cycle of clinical development for late-stage studies, including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. Specifically, The Director May Be Responsible For Planning clinical trials (design, operational plans, settings) based on these clinical development strategies Monitoring and managing the conduct of ongoing or new clinical...

This position works out of our Sturgis, MI location in the Abbott Nutrition division. Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® – to help them get the nutrients they need to live their healthiest lives. For over 70 years, Abbott’s Sturgis, Mich. , has been impacting its community while producing products that provide essential nutrition to millions of families around the world. Working...

*** This is an in-clinic position in Englewood, NJ *** A Natera Test Coordinator Phlebotomist serves patients by scheduling and identifying the best method for retrieving blood; preparing specimens for laboratory testing; and reconciling paperwork requirements as needed. PRIMARY RESPONSIBILITIES Split clinical and administrative duties Patient communications, including draw and timing requirements. Administrative duties, such as accessing patient information and reports in Electronic Medical Record (EMR), scheduling patients, aligning available blood draw times to clinic requirements, etc. Work from home time to be noted on timecard, submitted weekly Requires tracking and data entry for each drawcompleted, including billing information when...

Make a difference in patients' lives by applying your diagnostic and clinical test market expertise as a Precision Medicine Liaison! Key responsibilities include ensuring the timely, high quality in-market companion diagnostics / testing solutions are available to support optimal treatment. Engage collaborators before and after launch to provide approved information to proactively address barriers to testing at pre-specified region reference labs, pathology medical groups and a subset of academic/health system with well-developed diagnostic and molecular capabilities within assigned geography. Act as the regional expert to support oncology customers at the request of the cross functional team by providing more in-depth...

The 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...

This is a Remote Based position and will be covering a Southeast area (may not be limited to). Candidate must be located near an airport (Florida/Georgia/Alabama area -highly desirable locations). The successful candidate will be required to travel up to 80% of the time. The Senior CRA performs monitoring activities related to initiation, conduct (recruitment, quality data collection) and timely completion of Phase I-IV Pharma clinical trials within the country. The Senior CRA is responsible to deliver data within timelines and required quality standard, and adherence to monitoring procedures in accordance with ICH/GCP and US CFR and company SOPs. LI-#Remote...

Job Overview We are seeking a very experienced and highly motivated individual to join us as an Administrative Assistant to support the Site Head of our Manufacturing Operations as well as his team in La Verne, California. Provide administrative leadership and support to a large, highly matrixed Functional group requiring proactive coordination across the site while also working collaboratively with other site administrative staff. You may be asked to assist in areas outside of your primary responsibilities. The ideal candidate will be customer service oriented, flexible, proactive, a critical thinker and resourceful with a high level of professionalism, confidentiality, and...

Senior Therapy Development Specialist This position will work out of our Central Territory; Houston and/or Dallas region in the SH division. Structural Heart Business Mission Why We Exist Our business purpose is to restore health and improve quality of life by designing and providing device and management solutions for treating structural heart disease. As the Senior Therapy Development Specialist, you'll have the chance to work closely within the clinical study team including the medical director, program and project management, and other clinical study personnel as well as the commercial team. This position will have significant interaction with investigators, research...

Field Compliance Monitor - Manager/Sr. Manager (Healthcare Compliance Office) GLOBAL GRADE SE7 The Field Compliance Monitor leads and manages compliance monitoring activities across Genentech, with a focus on live (in-person and virtual) field-based activities (e.g., speaker programs and field ride-alongs) and field- related processes (e.g., account plans and call notes). The Field Compliance Monitor will travel Nationwide to monitor in-person field activities. CORE RESPONSIBILITIES Monitor in-person and virtual live events and activities, including but not limited to speaker programs, advisory boards, and field-based interactions with healthcare professionals, customers, and patients. Strategic planner in selecting, managing, and scheduling travel and appointments...

About Generate Biomedicines GenerateBiomedicines is a new kind of therapeutics company – existing at the intersection of machine learning, biological engineering, and medicine – pioneering Generative Biology™ to create breakthrough medicines where novel therapeutics are computationally generated, instead of being discovered. The Company has built a machine learning-powered biomedicines platform with the potential to generate new drugs across a wide range of biologic modalities. This platform represents a potentially fundamental shift in what is possible in the field of biotherapeutic development. We pursue this audacious vision because we believe in the unique and revolutionary power of generative biology to radically...

Clinical Research Medical Director What you will do In this vital role you will serve as clinical guide to provide clinical/scientific knowledge into the development, delivery and communication of the global scientific/medical evidence plan for the indication(s), primarily Thyroid Eye Disease (TED). Provide oversight of LCM clinical development with input on global strategy Medical monitoring for assigned clinical studies, including direct communication with Principal Investigators Support cross-functional and global collaborations to integrate broad medical, regulatory, safety, scientific, research, and commercial access, and value input into the development program(s) Participate and provide clinical input into safety and regulatory interactions. Review,...

Director, Clinical Research Our business purpose is to lead and shape the treatment of patients with structural heart disease via driving innovation, prioritizing clinical research, and championing product and procedural excellence. What You’ll Work On The Director of Clinical Programs will lead the portfolio of clinical trials including clinical trial strategy development and execution to support evidence generation for Abbott’s transcatheter mitral and tricuspid interventions (TMTI) portfolio. The individual will interact with multiple internal cross-functional teams, including R&D, medical affairs, regulatory affairs and finance to set the overall direction for the TMTI portfolio, and create/manage budgets, priorities and timelines. The...

Legend Biotech is seeking an Expert Clinical Research Scientist as part of the Clinical Development team based in Somerset, NJ. Role Overview The Clinical Research Scientist (CS) in Clinical Development is an important role in the company supporting the development and life cycle of drug development projects. The Clinical Research Scientist will work closely with the Clinical Trial Lead/Medical Lead and Clinical Operations Lead to design and implement clinical trial protocols and manage sites, CROs and other associated work. In addition, the CS will support their manager to ensure program consistency & alignment across studies, working closely with cross-functional teams...

About 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 We are searching for the best talent for a Senior Trial Supply Lead to be located in Titusville, NJ or Horsham, PA. Purpose Clinical Supply Chain (CSC) holds the responsibility of global clinical supplies of the Innovative Medicine Research...

At Caris, we understand that cancer is an ugly word—a word no one wants to hear, but one that connects us all. That’s why we’re not just transforming cancer care—we’re changing lives. We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day “What would I do if this patient were my mom?” That question drives everything we do. But our mission doesn’t stop with cancer. We're pushing the frontiers of medicine and leading a...

This position works out of our Plymouth, MN location in the EP division. In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. As the Senior Contract Coordinator, you'll have the chance to w ork cross-functionally to facilitate contracting with health care providers (HCP) to support the organization's operational needs. Perform a variety of specialized contract management activities to ensure the organization's agreements are legally sound, protect its business interests, and comply with all relevant laws and regulations. What...

Are you looking for a patient-focused, innovation-driven company to inspire you and empower you to shine? Join us as the Director, Clinical Trial Reporting based remotely reporting to the VP, Clinical Data Operations & Standards. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to work towards their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, and work toward excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by...