Clinical Research Project Manager - Breast Oncology Dana-Farber Cancer Institute IncClinical Research Project Manager - Breast OncologyBOSTON, MARemote$76,910–$85,295 / yearReporting to faculty, research and/or disease group managers, and/or Clinical Trials Office (CTO) leadership, the Clinical Research Project Manager I identifies project plan variances and develops contingency plans to maintain project milestones. Administrative Support: Schedule research team meetings and conference calls, facilitate mailings, and perform other project-related administrative tasks to ensure effective communication and coordination among team members and external collaborators.
Senior Medical Director, Clinical Research Neurology Sumitomo Pharma America Holdings Inc (Inactive)Senior Medical Director, Clinical Research NeurologyMarlborough, MA$284,320–$355,400 / yearSumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. Provide clinical input for and participate in study set up and design including data collection tools, data analysis, eCRF design, edit checks, vendor database design plans, etc.
Clinical Research Coordinator II - Lowell General Hospital, Cancer Center - On-site Tufts MedicineClinical Research Coordinator II - Lowell General Hospital, Cancer Center - On-siteLowell, MassachusettsThe 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.
Senior Director, In-Vivo & Non-Clinical Pharmacology, Research Business Insights & Technology Bristol-Myers Squibb CoSenior Director, In-Vivo & Non-Clinical Pharmacology, Research Business Insights & TechnologyMA$252,640–$306,137 / yearThis leader will partner deeply with Research leadership and the Pharmacology, DMPK, Toxicology, and Translational Science units to deliver the applications, workflow capabilities, AI, and supporting data flows that enable non-clinical decisions across in-vivo biology, DMPK, ADME, non-clinical safety, toxicology, and bioanalytical science. Reporting to the Vice President, Research Business Insights & Technology, this leader will operate as part of a unified BI&T leadership team and act as a trusted partner to Research leadership, translating scientific needs into scalable, integrated technology solutions.
NewSr. Manager/Associate Director, Clinical Monitoring Oversight Aura Biosciences Inc.Sr. Manager/Associate Director, Clinical Monitoring OversightBoston, MA$150,000–$215,000 / yearThis role is responsible for the strategic oversight of Clinical Research Associates (CRAs) and/or monitoring vendors (CROs), driving site performance, data quality, patient safety, and inspection readiness across all regions in which the trial(s) are conducted. Minimum 7-10 years of clinical research experience, including significant on-site or remote monitoring experience (CRA/Senior CRA background strongly preferred); typically, 3+ years in a lead CRA, monitoring management, or comparable oversight role for AD-level.
Senior Manager, Clinical Operations - Cardiology Iterative Scopes Inc.Senior Manager, Clinical Operations - CardiologyCambridge, MAAs the Senior Manager, Clinical Operations- Cardiology at Iterative Health you will serve as a strategic advisor to sponsors, CROs, and research sites, translating operational challenges into scalable solutions that improve study execution, accelerate activation timelines, and drive patient recruitment performance. By combining deep clinical research expertise with a consultative approach, this individual will help strengthen sponsor relationships, elevate site performance across the network, and contribute directly to Iterative Health's mission of bringing innovative therapies to patients faster.
NewSr. Manager/Associate Director, Clinical Monitoring Oversight Aura Biosciences IncSr. Manager/Associate Director, Clinical Monitoring OversightBoston, MA$150,000–$215,000 / yearThis role is responsible for the strategic oversight of Clinical Research Associates (CRAs) and/or monitoring vendors (CROs), driving site performance, data quality, patient safety, and inspection readiness across all regions in which the trial(s) are conducted. Minimum 7-10 years of clinical research experience, including significant on-site or remote monitoring experience (CRA/Senior CRA background strongly preferred); typically, 3+ years in a lead CRA, monitoring management, or comparable oversight role for AD-level.
NewSr. Manager, Clinical Trial Liaison - Remote Kiniksa Pharmaceuticals CorpSr. Manager, Clinical Trial Liaison - RemoteBoston, MARemote$170,000–$190,000 / yearThis role focuses on building strong relationships with investigative sites, identifying barriers to screening and enrollment, supporting protocol and operational education, ensuring contemporaneous and accurate data entry, and escalating site-level risks that may impact study execution, participant retention, data quality, or documentation readiness. Build and maintain productive relationships with Principal Investigators, study coordinators, research nurses, site managers, and other relevant site personnel, and serve as a sponsor representative and primary site engagement contact for assigned sites.
Senior Manager, Clinical Operations - Cardiology Iterative Scopes IncSenior Manager, Clinical Operations - CardiologyCambridge, MA$140,000–$165,000 / yearAs the Senior Manager, Clinical Operations- Cardiology at Iterative Health you will serve as a strategic advisor to sponsors, CROs, and research sites, translating operational challenges into scalable solutions that improve study execution, accelerate activation timelines, and drive patient recruitment performance. By combining deep clinical research expertise with a consultative approach, this individual will help strengthen sponsor relationships, elevate site performance across the network, and contribute directly to Iterative Health''s mission of bringing innovative therapies to patients faster.
Clinical Trial Associate II Prometrika LLCClinical Trial Associate IICambridge, MACTA/CTM, develop study specific processes to ensure that necessary study supplies are available at sites as required, coordinating with appropriate vendors as needed (i.e., Case Report Forms, Study Manuals, lab kits, drug supplies, lab supplies, etc.). The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical research projects, working with the study team in the initiation, maintenance and closeout of clinical projects according to GCP, ICH, CFR and SOPs/WPDs.
Associate Director of Epidemiology & Outcomes Research CorronaAssociate Director of Epidemiology & Outcomes ResearchWaltham, MassachusettsServe in the role of Clinical Research Manager (when needed), working directly with subscribers on research queries, which includes planning and leading meetings, developing project timelines and budgets, and working with the research team on issues related to study design and conduct. Responsibilities include working with Subscribers, supervising and mentoring the Clinical Research Managers, ensuring all deliverables are developed on time, and working with internal stakeholders representing the Epi Dept on initiatives that are cross functional.
Research Data Specialist - Breast Oncology Translational Research Dana-Farber Cancer Institute IncResearch Data Specialist - Breast Oncology Translational ResearchBOSTON, MA$50,500–$56,700 / yearDuties may include but are not limited to: the examination, synthesis, and evaluation of medical records; the abstraction and recording of pertinent medical information; retrieves archival tissue samples at outside institutions when relevant for translational studies; coordinates the collection, processing, organization, and storage of biological specimens (including but not limited to blood, tissue, stool); and the organization and collation of biospecimens collected within Breast oncology cohort studies. The Research Data Specialist (RDS) will support the Breast Oncology Cohort Studies clinical research program under the auspices of the Principal Investigator(s) and Associate Director of Translational Research, in the areas of identification, and collation of biospecimens associated with our departmental clinical data for studies.
Principal Carelon Research Biostatistician Elevance HealthPrincipal Carelon Research BiostatisticianNewton, Massachusetts$136,000–$234,600 / yearThis researcher partners with investigators, research sponsors, academic institutions, and cross-functional project teams to design studies, develop statistical methodologies, oversee analytical execution, and communicate scientific findings that advance externally funded clinical research programs. Experience designing clinical research studies, developing sample size calculations, statistical analysis plans, outcome measures, and advanced statistical methodologies including survival analysis, causal inference, and experimental design preferred.
NewResearch Nurse - Cancer Center South Shore HealthResearch Nurse - Cancer CenterWeymouth, MA$38.20–$77.39 / hourIn addition, the Research Nurse utilizes evidence-based nursing practice and has expertise in developing and coordinating a plan of care designed to meet the physical, psychological, and social needs of those cancer patients and their families undergoing therapy in a clinical research trial. Participates in Division of Nursing / Institute committees at the main DFCI Longwood campus, including, but not limited to, the monthly Research Nurse Practice Committee meeting.
Research Nurse - Cancer Center South Shore Health Systems IncResearch Nurse - Cancer CenterWeymouth, MA$38.20–$77.39 / hourIn addition, the Research Nurse utilizes evidence-based nursing practice and has expertise in developing and coordinating a plan of care designed to meet the physical, psychological, and social needs of those cancer patients and their families undergoing therapy in a clinical research trial. Participates in Division of Nursing / Institute committees at the main DFCI Longwood campus, including, but not limited to, the monthly Research Nurse Practice Committee meeting.
VP, Non-Interventional Research - Collections Research Iterative Scopes IncVP, Non-Interventional Research - Collections ResearchBoston, MAWork cross-functionally with site operations leaders and executive leadership to identify and onboard the right sites and networks network to stand up and support collections studies across different therapeutic areas and specialty networks. We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology.
Research Data Specialist - Center of Cancer Therapeutic Innovation Dana-Farber Cancer Institute IncResearch Data Specialist - Center of Cancer Therapeutic InnovationBOSTON, MARemote$50,500–$56,700 / yearWe strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. The Research Data Specialists will support the Center of Cancer Therapeutic Innovation (CCTI) clinical research program in the areas of data collection, computing, and database organization.
Research Nurse Float Dana-Farber Cancer Institute IncResearch Nurse FloatBOSTON, MA$42.65–$105.81 / hourIn addition, the CRN utilizes evidence-based nursing practice and has expertise in developing and coordinating a plan of care designed to meet the physical, psychological, and social needs of those cancer patients and their families undergoing therapy in a clinical research trial. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations.
Clinical Documentation Specialist Integrated Resources, IncClinical Documentation SpecialistLexington, MassachusettsFull timeJOB REQUIREMENTS: • Processing, filing and tracking of Trial Master File (TMF) documents (paper and/or electronic) in accordance with study-specific TMF Roadmaps. JOB SUMMARY: • Manages the Trial Master Files (all of the documents that support the clinical trials-everything that the FDA and regulatory agencies review).
Research Data Specialist - Breast Oncology Cohort Studies Program Dana-Farber Cancer Institute IncResearch Data Specialist - Breast Oncology Cohort Studies ProgramBOSTON, MARemote$50,500–$56,700 / yearWe strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. The Research Data Specialist (RDS) will support the Breast Oncology Cohort Studies clinical research program in the areas of data collection, computing, and database organization.