Head Of Clinical Operations, Vaccines SanofiHead Of Clinical Operations, VaccinesWaltham, MA$293,250–$423,583.33 / yearSelected candidate will possess a proven track record of leading large, multifunctional clinical operations teams in the pharmaceutical or biopharmaceutical industry, including experience managing global clinical trials across multiple regions. Contribute to the Global Clinical Development Leadership Team, contributing to the GCD 2030 Roadmap, championing continuous improvement in processes and ways of working, and ensuring the function evolves to meet future scientific and operational demands.
Clinical Trial Associate Candel Therapeutics Inc.Clinical Trial AssociateNeedham, MA$88,000–$100,000 / yearThis role includes working on multiple protocols with the potential to cross-train across different oncology indications using a variety of clinical trial databases. Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses.
Director, Pharmaceutical Sciences Clinical Manufacturing Business Operations 3316 Takeda Development Center AmericasDirector, Pharmaceutical Sciences Clinical Manufacturing Business OperationsLexington, MassachusettsProvide team leadership to ensure 1) PharmSci business processes are operating smoothly (CapEx, OpEx, Governance), 2) partner with Procurement to deliver year-over-years savings targets, and 3) support PharmSci in the development of SOWs, contracts and any additional purchasing support. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.
Clinical Systems Business Analyst Integrated Resources, IncClinical Systems Business AnalystLexington, MassachusettsFull timeJob Title: Clinical Systems and Technologies Business AnalystDuration: 5+ MonthsLocation: Lexington, MAJob Description:• Provide support within Clinical and other groups as required relating to company's Clinical Trials Management System (CTMS) to support Clinical business process, including design of reports to meet organizational needs, serving as CTMS Administrator, super-user and technical support.• Experience in testing and validation system enhancements and bug fixes; responsible for associated documentation• Experience in identifying report issues and ability to troubleshoot and fix• Experience leading workgroups to gather business requirements.•
Senior Clinical Director, Medical Management (2026-50362) University of MassachusettsSenior Clinical Director, Medical Management (2026-50362)Worcester, MAAll Academic Accounting & Finance Administrative Professional Administrative Support Advancement Basic Science Biotechnology Clinical Research Environmental Health & Safety Executive Faculty Healthcare Human Resources Information Technology Interns Library Maintenance and Facilities Management Nursing Office Assistant Other Post Doc Professional Technician I Public Safety Research Residents Retail & Dining Services Staff Assistant Staff Associate Volunteer. All Bedford Boston Brockton Brockton Canton Charlestown Danvers Devens Fall River Fitchburg Holyoke Jamaica Plain Jamaica Plan Lincoln Mattapan North Hampton North Quincy Pocasset Shrewsbury Springfield Taunton Tewksbury Waltham Westborough Westfield Woburn Worcester Wrentham.
Clinical Research Coordinator II - Lowell General Hospital, Cancer Center - On-Site Tufts MedicineClinical Research Coordinator II - Lowell General Hospital, Cancer Center - On-SiteLowell, MA$47,924.24–$59,894.75 / yearJob Profile Summary: The Clinical Research Coordinator supports clinical trials by recruiting and screening participants, conducting informed consent, and coordinating all protocol‑required visits, procedures, and follow‑up. Responsible for assisting with Institutional Review Board (IRB) requirements for each study including meeting institutional educational requirements, submitting documents for review, adverse event reporting and annual reviews.
Sr Clinical Research Assistant Brown University HealthSr Clinical Research AssistantProvidence, RI$48,068.80–$79,372.80 / yearThe core Success Factors include: Instill Trust and Value Differences Patient and Community Focus and Collaborate RESPONSIBILITIES: Identifies patients meeting criteria for inclusion in clinical research studies, ensuring research protocol eligibility requirements are met. May provide functional guidance to subordinate research staff assigned to the project to provide clarification of protocol, resolve issues, ensure adherence to research protocol procedures and assist in developing their professional skills in reviewing and interpreting statistical trends and the like.
Clinical Pharmacist- Outpatient Prescription Center, Per Diem UMass Memorial Health Care IncClinical Pharmacist- Outpatient Prescription Center, Per DiemWorcester, MA$46.26–$83.26 / hourMajor Responsibilities: The following key performance areas (Clinical, Operations/Distribution, Financial, Safety and Regulatory, Research and Education) are performed by the clinical pharmacist: Clinical Performance: Provides medication management services in a collaborative manner that consist of the following: Review patient medication history, educate patients on drug therapy, establish desired outcomes, develop/modify therapeutic plans, determine alternatives for achieving outcomes, develop drug monitoring plans, monitor patient outcomes, document medication related issues in electronic health record, interpret laboratory data, review patient medication profiles, monitor pharmacokinetics of drug therapy, monitoring for potential adverse drug - drug, drug-lab, drug-disease state, and drug - food interactions. Precepts Intermediate Pharmacy Practice Experience (IPPE) rotation students, and Advanced Pharmacy Practice Experience (APPE) rotation students, and pharmacy residents consistent with academic credentials and clinical experience.
Clinical Pharmacist, Ambulatory (Family Medicine & Pediatrics), 32hr, Day UMass Memorial Health Care IncClinical Pharmacist, Ambulatory (Family Medicine & Pediatrics), 32hr, DayWorcester, MA$96,220.80–$173,180.80 / yearProvides medication management services in a collaborative manner that consist of the following: Review patient medication history, educate patients on drug therapy, establish desired outcomes, develop/modify therapeutic plans, determine alternatives for achieving outcomes, develop drug monitoring plans, monitor patient outcomes, document medication related issues in electronic health record, interpret laboratory data, review patient medication profiles, monitor pharmacokinetics of drug therapy, monitoring for potential adverse drug - drug, drug-lab, drug-disease state, and drug - food interactions. Precepts Intermediate Pharmacy Practice Experience (IPPE) rotation students, and Advanced Pharmacy Practice Experience (APPE) rotation students, and pharmacy residents consistent with academic credentials and clinical experience.
Clinical Pharmacist Decentralized, Internal Medicine, 40hr, Day UMass Memorial Health Care IncClinical Pharmacist Decentralized, Internal Medicine, 40hr, DayWorcester, MA$96,220.80–$173,180.80 / yearProvides medication management services in a collaborative manner that consist of the following: Review patient medication history, educate patients on drug therapy, establish desired outcomes, develop/modify therapeutic plans, determine alternatives for achieving outcomes, develop drug monitoring plans, monitor patient outcomes, document medication related issues in electronic health record, interpret laboratory data, review patient medication profiles, monitor pharmacokinetics of drug therapy, monitoring for potential adverse drug - drug, drug-lab, drug-disease state, and drug - food interactions. Precepts Intermediate Pharmacy Practice Experience (IPPE) rotation students, and Advanced Pharmacy Practice Experience (APPE) rotation students, and pharmacy residents consistent with academic credentials and clinical experience.
Oncology Clinical Pharmacist, Outpatient Infusion Center, 40hr, Day UMass Memorial Health Care IncOncology Clinical Pharmacist, Outpatient Infusion Center, 40hr, DayWorcester, MA$96,220.80–$173,180.80 / yearProvides medication management services in a collaborative manner that consist of the following: Review patient medication history, educate patients on drug therapy, establish desired outcomes, develop/modify therapeutic plans, determine alternatives for achieving outcomes, develop drug monitoring plans, monitor patient outcomes, document medication related issues in electronic health record, interpret laboratory data, review patient medication profiles, monitor pharmacokinetics of drug therapy, monitoring for potential adverse drug - drug, drug-lab, drug-disease state, and drug - food interactions. Precepts Intermediate Pharmacy Practice Experience (IPPE) rotation students, and Advanced Pharmacy Practice Experience (APPE) rotation students, and pharmacy residents consistent with academic credentials and clinical experience.
Clinical Pharmacist, Inpatient Pharmacy, Per Diem UMass Memorial Health Care IncClinical Pharmacist, Inpatient Pharmacy, Per DiemWorcester, MA$46.26–$83.26 / hourMajor Responsibilities: The following key performance areas (Clinical, Operations/Distribution, Financial, Safety and Regulatory, Research and Education) are performed by the clinical pharmacist: Clinical Performance provides medication management services in a collaborative manner that consist of the following: Review patient medication history, educate patients on drug therapy, establish desired outcomes, develop/modify therapeutic plans, determine alternatives for achieving outcomes, develop drug monitoring plans, monitor patient outcomes, document medication related issues in electronic health record, interpret laboratory data, review patient medication profiles, monitor pharmacokinetics of drug therapy, monitoring for potential adverse drug - drug, drug-lab, drug-disease state, and drug - food interactions. Research and Education Performance Precepts Intermediate Pharmacy Practice Experience (IPPE) rotation students, and Advanced Pharmacy Practice Experience (APPE) rotation students, and pharmacy residents consistent with academic credentials and clinical experience.
RN Clinical Coordinator (2026-50386) University of MassachusettsRN Clinical Coordinator (2026-50386)Worcester, MAAll Academic Accounting & Finance Administrative Professional Administrative Support Advancement Basic Science Biotechnology Clinical Research Environmental Health & Safety Executive Faculty Healthcare Human Resources Information Technology Interns Library Maintenance and Facilities Management Nursing Office Assistant Other Post Doc Professional Technician I Public Safety Research Residents Retail & Dining Services Staff Assistant Staff Associate Volunteer. Under the general direction of the Associate Director, or designee, the Clinical Coordinator is responsible to develop, prioritize, and oversee staff activities specifically designed to promote the coordination of care for those MassHealth members who have medically complex, chronic or catastrophic illnesses that require a customized approach to how, when, and where they receive medically necessary health care services.
Clinical Documentation Specialist Integrated Resources, IncClinical Documentation SpecialistLexington, MassachusettsTemporaryJob DescriptionTitle: Clinical Documentation SpecialistLocation: Lexington, MADuration: 6 months (possible extension)JOB SUMMARY:• Manages the Trial Master Files (all of the documents that support the clinical trials-everything that the FDA and regulatory agencies review)• Support group for clinical, data managing, medical writing, safety, clinical supplies (Global Clinical Development Operations)JOB REQUIREMENTS:• Processing, filing and tracking of Trial Master File (TMF) documents (paper and/or electronic) in accordance with study-specific TMF Roadmaps• Performing quality checks of TMF documents as needed• Providing oversight of TMF quality checks performed by functional areas and/or CRO's• Assisting with audit and inspection preparation as applicableMUST HAVE:• 2 years minimum experience doing anything associated with TMF (Trial Master Files) or Clinical Documentation• GCP Experience preferred• clinical experience• CTA/CRA experience OK• Experience with using an electronic document management system and proficient in excel necessaryQualifications• 2 years minimum experience doing anything associated with TMF (Trial Master Files) or Clinical Documentation• GCP Experience preferred• clinical experience• CTA/CRA experience OK• Experience with using an electronic document management system and proficient in excel necessary Clinical Documentation SpecialistA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Clinical Information Analyst Integrated Resources, IncClinical Information AnalystLexington, MassachusettsContractorThe role will work closely with Subject Matter Experts to define requirements, analyze and compare multiple systems for usability, strategize and implement data migration from legacy systems to new systems. Job DescriptionDuration: 10 months + ContractPOSITION RESPONSIBILITIES:Clinical Information Analyst will be responsible for supporting disposition of legacy clinical systems and data integration to new Client clinical systems.
Clinical Supply Associate Integrated Resources, IncClinical Supply AssociateLexington, MassachusettsFull timeEnsure that goals and objectives of projects are accomplished within established time frames and budget guidelines.• Ensure compliance with Good Manufacturing Practices and applicable state and federal regulatory authorities• Participate in protocol review to identify clinical issues; establish time frames; develop budget projections; identify procedural and administrative issues; recommend amendments to study protocols as appropriate.• Manage clinical supply activities including labeling, packaging, distribution of clinical trial supplies, randomization, development and maintenance of clinical trial database and drug accountability systems control.•
Associate Director, Clinical Research Scientist (Neurology) Alkermes PlcAssociate Director, Clinical Research Scientist (Neurology)Waltham, MAIn 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts' Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.
Clinical Research Assistant UMass Chan Medical SchoolClinical Research AssistantWorcester, MAGENERAL SUMMARY OF POSITION: Under the direction of the Principal Investigator or designee, the Clinical Research Assistant is responsible for performing delegated tasks and procedures involving human subjects in support of clinical research protocols. Maintain appropriate operations as needed including to stock, inventory, store, and order samples/supplies.
NewClinical Study Specialist IREClinical Study SpecialistWarren, MassachusettsCompiles study manuals including but not limited to: study reference binders and manuals and maintains versioning of study reference materials (e.g., regulatory, pharmacy, and laboratory binders. Tracks and monitors close out activities – study close-out documents (1572s, Investigational Product reconciliation, Financial Disclosures, etc.) and CRA close-out visits.
Director, Clinical Operations, Oncology 3316 Takeda Development Center AmericasDirector, Clinical Operations, OncologyMassachusettsOversight of Strategic Partners/CRO/vendor selection, budget and contract negotiation, and proper supervision of performance for all activities assigned to a Strategic Partner/CRO/vendor for assigned program(s), including escalation of issues to and participation in governance committees; accountable for operational risk management strategy in collaboration with Strategic Partners. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.