86 director of tax jobs found

job summary: The Real World Evidence Leads are part of the Medical Evidence Generation function comprised of subject matter experts in evidence planning, study design and data interpretation. The function works to drive excellence in evidence planning and implement novel study design approaches to generate robust evidence to enhance understanding of unmet medical need; support patient and endpoint selection for Clinical studies; and inform clinical practi

job summary: Sr. Pharmacovigilance (PV) Operations Manager | Remote | West Coast This critical role is responsible for managing and overseeing PV operations across clinical development programs, ensuring seamless collaboration with PV vendors. You will play a key role in preparing for the initiation of two global Phase 3 trials, ensuring all PV activities are in place. Your expertise in global trial management, study document review, and vendor oversight

job summary: We are seeking a Sr. Data Analyst to join the Clinical Systems Analytical & Reporting (CSAR)-Analytics team within Global Development Operations. This role will enhance our analytical reporting capabilities and support business continuity across multiple clinical system technology enhancement projects. Key responsibilities include contributing to analytics initiatives supporting critical business functions relying on data from eTMF, EDC, CTMS

job summary: This is a high level contract role, requiring Direct Global Regulatory Labeling Operations Project Management experience in the Pharma/Biotech industry, as deep knowledge of pharmaceutical labeling regulations, compliance, and processes are critical for this role. The Labeling Project Manager is responsible for all activities associated with the development, creation and execution of labeling for assigned product lines for domestic and/or i

job summary: The Senior Manager/Associate Director, Medical Communications Ad Promo, represents the Medical function in the Material Review Process to guarantee medical, clinical, and scientific data accuracy, relevance, objectivity, balance and alignment with product label. Functions as the lead medical reviewer and sign-off for all promotional materials in designated area(s) of responsibility. Provides proactive guidance as needed for brand concepts and

job summary: This position is for a major Pharmaceutical company whose purpose is to transform the practice of medicine through breakthrough science and make a positive impact on our people and the communities we serve. Chasing the miracles of science to improve people's lives, Join us to make a positive impact in health care!! KEY SKILLS: Upstream group - cell culture development experienceBio reactor operations - Ambr15, ambr250 etc.Bench-scale experi

job summary: We are seeking a highly skilled and experienced Senior QA Specialist to join our dynamic team. In this role, you will be responsible for overseeing the quality assurance process, supporting batch disposition of drug substance, ensuring that our products meet both Local and Global quality standards. location: Cambridge, Massachusetts job type: Contract salary: $59.00 - 61.63 per hour work hours: 9 to 5 education: Bachelors resp

job summary: The Global Regulatory Affairs and Drug Safety (GRADS) Alliance Management Summer Internship opportunity is designed to expose a selected individual to the roles and responsibilities of alliance and vendor management within the pharmaceutical industry setting. The selected individual will gain exposure to alliance and vendor management processes such as business partner agreements and commitment reporting, pharmacovigilance exhibits, and vendo

job summary: The Cell Culture Manufacturing Senior Technician position will directly enable the initial start-up phase of the Hopewell manufacturing facility and then shift focus to hands-on execution and support of cGMP manufacturing operations. location: Pennington, New Jersey job type: Contract salary: $45.13 - 53.10 per hour work hours: 9 to 5 education: High School responsibilities: Hands-On cGMP Operations: Focused on execution of c

job summary: Global Labeling Manager - Regulatory Affairs REMOTE | EST Hours Join a mission-driven team committed to ensuring the safe and effective use of pharmaceutical products worldwide. We're seeking a Global Labeling Manager with a passion for regulatory excellence, precision, and cross-functional collaboration. About the Role: As a Global Labeling Manager, you will drive global labeling strategy and ensure high-quality, compliant labeling documents

Onsite in Billerica, MA 9:00 AM-6:30 PM, with some weekend work. Provide oversight and technical guidance for daily Outbound Shipment operations ensuring the safe, legal tender of products to our carriers. Responsible to ensure compliance with all relevant distribution laws and regulations. Accountable for the accuracy and traceability for the products in preparation for the shipment process to the transportation carrier network. salary: $25 - &#

Onsite in Bedford, MA 3 days per week. Must have Order Management Systems experience. The Business Analyst for the Commercial Order Management Systems (OMS) plays a pivotal role in bridging the gap between business needs and technology solutions. This role involves gathering, analyzing, and documenting business requirements for the OMS, ensuring the system effectively supports the order management process for radio pharmaceutical products. The Business A

job summary: Are you a data-driven scientist looking to apply your coding and molecular biology expertise in the biotech industry? This Data Scientist I (Clinical) role offers an exciting opportunity to work hands-on with research scientists to develop automated workflows, manage raw data processing, and enhance digital tracking systems. You'll spend 25% of your time coding in Python, integrate cutting-edge data solutions, and play a key role in optimizin

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowled

job summary: We are seeking a Clinical Site Contracts Specialist to manage end-to-end processes for clinical site contracts and consulting agreements, ensuring smooth study start-up and trial operations. If you're detail-oriented, proactive, and passionate about negotiation and collaboration, this is your chance to contribute to critical clinical research initiatives. Apply today to take the next step in your career-let's start the conversation! locati

job summary: Biologics Developability Screening and Automation The Biologics CMC Developability team is an integral part of the Biologics CMC Drug Product Development organization at Company. The Biologics CMC Developability team is responsible for- (1) the identification of biophysical- and chemical liabilities in discovery-stage biologic drug candidates to guide lead selection, and (2) for characterization of the key CMC attributes important for biologi

job summary: The Device Tracking Analyst will communicate with customers to obtain and/or verify device tracking information in compliance with device tracking regulations established by the FDA and international regulatory bodies. He/she will facilitate actions identified to improve customer experience and patient safety. He/she will participate and/or lead in the identification and implementation of device tracking management system improvements, includ

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines

job summary: This role provides site-wide support for clinical lab operations activities. Responsibilities will include the installation, maintenance, and sustained performance of cutting- edge laboratory equipment along with documenting activities in accordance with regulatory compliance guidelines. Laboratory equipment supported will range widely, but will include next- generation sequencing platforms and automated liquid handling robots. This position

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longti

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus

Join a leading biopharmaceutical company as a Research Associate supporting a fastpaced, highly automated genomics lab. You'll work with a large, collaborative team to support genotyping efforts critical to agricultural innovation and crop genome editing. This is an ideal role for those with strong attention to detail, a technical mindset, and a passion for lab operations.salary: $27 - $35 per hourshift: Firstwork hours: 2 PM - 10 PMeducation: As

job summary: Randstad Life Sciences is seeking a Process Engineer III to join one of our client's engineering teams within a growing, FDA-regulated pharmaceutical manufacturing environment. This individual will play a key role in the development, scale-up, and validation of novel drug delivery products, supporting both commercial and developmental production. location: York, Pennsylvania job type: Permanent salary: $95,000 - 110,000 per year w

job summary: Immediate opening for a QA Frontline Associate (Night Shift) to support the Technical Operations team at a leading, global pharmaceutical company specializing in rare diseases. The Technical Operations group is responsible for creating drugs for use in clinical trials and for scaling production of those drugs for the commercial market. The QA Frontline team is committed to providing real time QA support to the manufacturing facilities by perf

job summary: Title: Global Case Management Specialist Location: Remote Reports to: Sr. Manager, PV Operations Global Case Management The Global Case Management Specialist will be responsible for effective execution of the activities of triage, processing, and quality control of individual case safety reports (ICSR) from clinical trials to ensure timely and accurate assessment of adverse event reports. This role will focus on accurate case entry and w

job summary: The Process Engineer IV provides expert technical support to biologics downstream manufacturing, ensuring robust, compliant, and optimized processes. This role drives performance through data analysis, problem-solving, and cross-functional collaboration in a GMP environment. One - Year Contract 100% on-site in Framingham, MA location: Framingham, Massachusetts job type: Contract salary: $85 - 88 per hour work hours: 9 to 5 educa

job summary: Sr. Manager, Clinical Supplies (Oral Solid Dose) 6 Month Contract (may extend or convert) Remote (75%) + 1 week / month in South SF Looking for West Coast Based Candidates (travel reimbursed) Must Have: Experience with oral tablet dosage form Phase 1 & Small Biotech experience APAC logistics experience is a plus Strong MS Excel skills Seeking a talented, independent, and highly motivated Senior Manager, Clinical Supplies Planning

job summary: Shift: Monday-Friday, 7am-3pm. Fully onsite position location: Ridgefield, New Jersey job type: Contract work hours: 9 to 5 education: Bachelors responsibilities: Perform operations necessary for calibration of equipment that may include testing, adjusting, and maintaining measuring and indicating instruments to conform to set standards.Monitor and verify quality in accordance with statistical process or other control procedures

Join the team at MilliporeSigma, a global leader in life science innovation. Our Danvers facility specializes in the production of single-use bioprocessing assemblies used in the development of life-saving therapies and vaccines. We are currently hiring reliable and detail-oriented Assemblers to support our cleanroom manufacturing operations. Responsibilities: Assemble single-use components such as filters, tubing, and sterile bags Follow written in

job summary: Immediate opportunity for a Sr. Regulatory Affairs Associate, CMC to assist the technical team in preparing regulatory filing dossiers, assess changes for regulatory impact, and manage documentation systems. You will participate in Global Regulatory Product Team (GRPT) and Operations Brand Team meetings as needed. As a Senior Associate, RA CMC, you will work with internal and external partners in order to deliver products to patients. Prepare