NewFamily Medicine Physician Needed for Locum Tenens Coverage in Massachusetts LocumTenens.comFamily Medicine Physician Needed for Locum Tenens Coverage in MassachusettsSpencer, MAThe facility is supported by a multidisciplinary team that includes RNs, LPNs, NPs, MDs, mental health clinicians, PMHNPs, dentistry, optometry, dialysis, physical therapy, nurse managers, discharge planners, medical assistants, phlebotomy, lab, and X-ray staff. About the Facility Location Massachusetts offers a range of regional attractions and year-round opportunities for outdoor recreation, cultural experiences, and exploration throughout its diverse towns and communities.
Clinical Trial Manager/Senior Clinical Trial Manager Oruka Therapeutics IncClinical Trial Manager/Senior Clinical Trial ManagerWaltham, MA$146,000–$161,000 / yearOruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Key Responsibilities: Clinical Trial Management: Lead and manage multiple clinical trials from initiation through to completion, ensuring adherence to study timelines and budgets.
Sr./Clinical Trial Manager - Clinical Operations Aktis Oncology IncSr./Clinical Trial Manager - Clinical OperationsBoston, MAAktis' most-advanced program, AKY-1189, is a miniprotein radioconjugate targeting Nectin-4, with multi-indication potential across multiple tumor types, including locally advanced or metastatic urothelial cancer, breast cancer, non-small cell lung cancer, colorectal cancer, cervical cancer, and head and neck cancer. Aktis Oncology, Inc. is a clinical-stage oncology company focused on expanding the breakthrough potential of targeted radiopharmaceuticals to large patient populations, including those not addressed by existing platform technologies.
Senior Clinical Trial Manager / Clinical Trial Manager Verastem IncSenior Clinical Trial Manager / Clinical Trial ManagerBoston, MA$115,000–$130,000 / yearLiaise with medical monitor and cross functional team members as necessary and in accordance with established SOPs to produce study deliverables (e.g., clinical protocols, CRFs, informed consent templates, project management plan, data management plan, safety management plan, medical monitoring plan, clinical monitoring plan, pharmacy/lab manuals, clinical study reports etc.). Company Profile: At Verastem Oncology, were advancing innovation and addressing the urgent needs of patients living with cancers driven by RAS/MAPK pathway mutations, a key driver of tumor growth and treatment resistance.
Clinical Trial Manager Kymera TherapeuticsClinical Trial ManagerWatertown, MA$115,000–$200,000 / yearHaving advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Work closely with translational medicine team to ensure appropriate incorporation of bioanalytical sampling plan into clinical protocols and relevant data output of the trial is provided to functional groups for review.
Clinical Trial Manager/Senior Clinical Trial Manager Oruka TherapeuticsClinical Trial Manager/Senior Clinical Trial ManagerWaltham, MassachusettsOruka’s mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Team Leadership: Drive the cross functional internal study team ensuring appropriate alignment, risk management and coordination across all participating functions.
NewSenior Clinical Trial Manager Actalent IncSenior Clinical Trial ManagerWaltham, MA$88–$103 / hourThe Senior Clinical Trial Manager serves as the Clinical Operations lead on cross-functional teams, driving operational excellence across study start-up, site activation, monitoring, and enrollment for a global Phase III trial in the rare disease and neuromuscular space. Collaborate closely with cross-functional teams, including Clinical Operations, Development, vendors, investigators, and study sites, to resolve issues and maintain operational momentum.
Clinical Trial Manager Care AccessClinical Trial ManagerBoston, MARemote$90,000–$110,000 / yearWith programs like Future of Medicine , which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers , which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The CTM is responsible to drive the successful execution of protocols or projects, including within the decentralized trial model when applicable, from strategic planning through close out within agreed upon timelines, budget, alignment with all applicable SOPs and regulatory requirements.
Clinical Trial Manager Kymera Therapeutics IncClinical Trial ManagerWatertown, MA$115,000–$200,000 / yearHaving advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Work closely with translational medicine team to ensure appropriate incorporation of bioanalytical sampling plan into clinical protocols and relevant data output of the trial is provided to functional groups for review.
Senior Clinical Trial Manager (Global) Bicara TherapeuticsSenior Clinical Trial Manager (Global)Boston, MassachusettsFICERA specifically addresses a key challenge in solid tumor treatment by enabling immune cell penetration into tumors, reducing fibrosis and immunosuppression while reversing TGF--driven resistance mechanisms - ultimately designed to drive the deep, durable responses that may translate into better outcomes and survival for patients. Founded in 2020, we've built a global team of over 100 employees headquartered in Boston, with a clear focus on advancing our lead asset, ficerafusp alfa, or FICERA - a potentially first-in-class bifunctional EGFR-directed antibody combined with a TGF- ligand trap.
Regional Clinical Trial Manager - East Coast, US PrileniaRegional Clinical Trial Manager - East Coast, USBoston, MassachusettsRemoteThis is a critical individual contributor role in a growing biotech company, suitable for a candidate who is equally comfortable working independently across multiple projects and while collaborating in a matrix global team environment. Ability to work across multiple projects with demonstrated ability to manage CROs (and other vendors) to meet or exceed KPIs tied to corporate goals and hold them accountable if they fall behind.
NewSenior Clinical Trial Manager Treeline Biosciences IncSenior Clinical Trial ManagerWatertown, MA$153,000–$197,600 / yearJob responsibilities include, but are not limited to, preparation of study related materials, enrollment tracking and reporting, relationship management with study sites and vendors (in particular CROs), supervision of study-related activities, identification of project risks and contingency planning. Unsolicited resumes sent to Treeline Biosciences from recruiters do not constitute any type of relationship between the recruiter and Treeline Biosciences and do not obligate Treeline Biosciences in any way to pay fees should we hire from those resumes.
Clinical Trial Manager Prometrika LLCClinical Trial ManagerCambridge, MAExperience working in cross-functional teams and direct involvement in protocol and CRF development is highly valued Proven track record of ensuring GCP/regulatory/protocol compliance, managing timelines and budgets, leading risk assessments, and implementing CAPAs and KPIs SKILLS Working knowledge of the clinical drug development process Strong knowledge of clinical research operations, including interpretation and implementation of FDA regulations/ICH guidelines Strong analytical and problem-solving skills Written, verbal communication and presentation skills in small and large group settings Must possess excellent interpersonal skills Mentoring/coaching Ability to effectively multi-task and prioritize Organizational skills and attention to detail required Solid computer skills requirement of MS applications including (but not limited to) MS Project, Word, Excel, PowerPoint Cross functional and cross-cultural awareness Ability to work in a matrix environment. RESPONSIBILITIES The Clinical Trial Manager (CTM) works closely with various sponsors, internal team members and vendors as well as clinical study sites to ensure that clinical trials are conducted in a timely fashion and in a manner compliant with SOPs, ICH/GCP/regulatory guidelines, study protocol, company goals, and budgets.
Senior Clinical Trial Manager - Boston, MA (M/F/X) Tissium SASenior Clinical Trial Manager - Boston, MA (M/F/X)Boston, MAAssumes overall responsibility for the development of protocols, clinical literature reviews, clinical trial reports, annual reports, risk/benefit analyses, informed consent templates, and other clinical documents. This individual will be responsible for study timelines and budgets, preparation of study-related materials, relationship management between study sites and CROs, supervision of study activities, identification of project risks, and contingency planning.
NewClinical Trial Manager Acrivon Therapeutics IncClinical Trial ManagerWatertown, MAThese distinctive capabilities enable the company to go beyond the limitations of traditional drug discovery, as well as current AI-based target-centric drug discovery and rapidly design highly differentiated compounds with desirable pathway effects through intracellular protein network analyses and advance these agents into the clinic for streamlined development. Minimum of 3+ years of Clinical Operations and Clinical Trial Management experience at a contract research organization, biotech or pharmaceutical company preferably in early to mid-phase oncology Proven leadership skills managing cross-functionally in a matrix environment.
Clinical Trial Manager Centessa Pharmaceuticals PlcClinical Trial ManagerBoston, MA$120,000–$150,000 / yearDrive critical study milestones, including site activation, enrollment progress, patient retention, data cleaning, and database lock, proactively addressing operational challenges common to CNS trials. Lead day‑to‑day clinical trial operations, coordinating cross‑functional partners (Clinical Development, Data Management, Biostatistics, Regulatory, Safety) to ensure efficient trial execution and alignment to program objectives.
Senior Clinical Trial Manager (Contract) TransMedics Group IncSenior Clinical Trial Manager (Contract)Andover, MA8-10 years experience in medical device (strongly preferred), pharmaceutical drug development, biotech or CRO industries monitoring and managing clinical trials (cardiovascular therapeutic indications preferred); or equivalent combination of education and experience. The Senior Clinical Trial Manager (Contract role) will be responsible for overseeing all operational phases of clinical research, from start-up to database lock, ensuring studies are completed on time, within budget and in compliance with ICH-GCP guidelines and regulations.
Principal Clinical Trial Manager TransMedicsPrincipal Clinical Trial ManagerAndover, MassachusettsThis position is responsible for, but not limited to, the following: Leading the process of pre and post market clinical trials for FDA by employing effective organizational strategies and reviewing and presenting the results using rigorous clinical procedures . Experience in medical device (strongly preferred), Outstanding track record leading large complex global clinical trials for medical device products in different phases of the product cycle .
Assistant Clinical Research Manager - Breast Oncology Clinical Trials Dana-Farber Cancer Institute IncAssistant Clinical Research Manager - Breast Oncology Clinical TrialsBOSTON, MA$70,000–$85,300 / yearThese positions, in collaboration with the program's Clinical research Managers physicians and research nursing staff, are responsible for assisting with the design, implementation and evaluation of their program's clinical research activities, related regulatory oversight, and will provide day to day supervision of their program's clinical research staff as needed. This Assistant Clinical Research Manager (ACRM) position will work within the Breast Oncology clinical research program and assist in the management of the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator.
Assistant Clinical Research Manager - Center of Early Detection & Intervention Blood Cancers Interventional Clinical Trials Dana-Farber Cancer Institute IncAssistant Clinical Research Manager - Center of Early Detection & Intervention Blood Cancers Interventional Clinical TrialsBOSTON, MARemote$70,000–$85,300 / yearThe Assistant Clinical Research Manager (ACRM) position will work within the Center of Early Detection & Intervention Blood Cancers (CEDI BC) Interventional Clinical Trials clinical research program and assist in the management of the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. These positions, in collaboration with the program's Clinical research Managers physicians and research nursing staff, are responsible for assisting with the design, implementation and evaluation of their program's clinical research activities, related regulatory oversight, and will provide day to day supervision of their program's clinical research staff as needed.
Senior Clinical Trial Manager Eight Sleep IncSenior Clinical Trial ManagerBoston, MA$140,000–$175,000 / yearThis is a hands-on, operationally intense position for someone who knows how to stand up a study from scratch, manage third-party clinical sites, write IRB and informed consent documents, oversee data management, and drive studies to completion on time and on budget. Collaborate cross-functionally with regulatory affairs, product, engineering, data science, and legal teams to ensure clinical strategies align with product development and submission timelines.
Principal Clinical Trial Manager TransMedics Group IncPrincipal Clinical Trial ManagerAndover, MA$137,100–$193,700 / yearThis position is responsible for, but not limited to, the following: Leading the process of pre and post market clinical trials for FDA by employing effective organizational strategies and reviewing and presenting the results using rigorous clinical procedures. Experience in medical device (strongly preferred), Outstanding track record leading large complex global clinical trials for medical device products in different phases of the product cycle.
Senior Clinical Trial Manager Entrada TherapeuticsSenior Clinical Trial ManagerBoston, MassachusettsRemote$160,000–$185,000 / yearWe are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51).
Senior Clinical Trial Manager Eight SleepSenior Clinical Trial ManagerBoston, MassachusettsThis is a hands-on, operationally intense position for someone who knows how to stand up a study from scratch, manage third-party clinical sites, write IRB and informed consent documents, oversee data management, and drive studies to completion on time and on budget. Collaborate cross-functionally with regulatory affairs, product, engineering, data science, and legal teams to ensure clinical strategies align with product development and submission timelines.
Senior Clinical Trial Manager Entrada Therapeutics IncSenior Clinical Trial ManagerBoston, MARemote$160,000–$185,000 / yearWe are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51).
Sr. Clinical Trial Manager, Therapeutics and Oncology ModernaTXSr. Clinical Trial Manager, Therapeutics and OncologyPrinceton, MassachusettsWe are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. Review and provide clinical operations input into relevant clinical documents such as the protocol, investigator brochure, regulatory documents, clinical study reports and other documents and plans as appropriate.
Sr. Manager - Clinical Trial Lead Biogen IncSr. Manager - Clinical Trial LeadMA$141,000–$188,000 / yearThe Senior Manager, CTL, leverages their phase, indication and operational expertise to independently manage and ensure delivery of one or more clinical studies, including: Partnering with cross-functional representatives to drive the development of operationally feasible and robust protocol designs, ensuring that principles of patient focus, risk management, quality and scientific integrity are applied, exercising appropriate budget responsibility and focused, endpoint-driven cost consideration. As required, collaborates strategically with the core SMT (study MD, biostatistics, etc.) and other key program team members to provide direction on phase, disease, or therapeutic area to support study design in alignment with the Integrated Asset Plan (IAP) and Program Operational Plan (POP), enabling protocol concept development and driving forward studies through governance approval.
Senior Category Manager - FSP & Clinical Trial Enablement Biogen IncSenior Category Manager - FSP & Clinical Trial EnablementCambridge, MA$129,000–$173,000 / yearIn this pivotal role, you will oversee global spend in key clinical and development areas such as Study Management & Monitoring (SM&M), Functional Service Provider (FSP) models, site enablement, patient-facing services, and ancillary support. Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
Senior Category Manager – FSP & Clinical Trial Enablement BiogenSenior Category Manager – FSP & Clinical Trial EnablementCambridge, MassachusettsIn this pivotal role, you will oversee global spend in key clinical and development areas such as Study Management & Monitoring (SM&M), Functional Service Provider (FSP) models, site enablement, patient-facing services, and ancillary support. Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
Senior Clinical Trial Manager ArtbioSenior Clinical Trial ManagerCambridge, MassachusettsThe successful candidate will manage members of the clinical operations team, including those at CROs and study vendors, work collaboratively with clinical trial sites, and partner with key internal stakeholders to ensure clinical trial deliverables are completed on time, within budget, and in line with regulatory requirements. Lead the oversight of CROs and vendors in partnership with the rest of the Clinical Operations team to assure the integrity of clinical data with respect to accuracy, accountability, and documentation through review of case report forms, source documents, medical records, etc.
Sr Manager, Case Mgmt, Clinical Trial Safety BiogenSr Manager, Case Mgmt, Clinical Trial SafetyCambridge, MassachusettsRegular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. The Sr Manager Case Management, Clinical Trial Safety will be responsible for managing the in-house case processing of clinical trial safety reports (and some post-market reports) in Biogen’s safety database.
(Sr.) Clinical Trial Manager Third Rock Ventures LLC(Sr.) Clinical Trial ManagerCambridge, MAfor more information visit urlhttps://recruiting.paylocity.com/Recruiting/Jobs/Details/4260950.
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.
Senior Clinical Trial Manager Kailera TherapeuticsSenior Clinical Trial ManagerWaltham, MassachusettsServe as the primary operational lead for assigned clinical trials, accountable for end-to-end trial execution, including oversight of CROs and vendors from study start-up through close-out. This role requires a proactive, solution-oriented professional who can collaborate cross-functionally and manage external partners with minimal oversight.
Clinical Trial Associate, Clinical Operations, Infectious Disease ModernaTXClinical Trial Associate, Clinical Operations, Infectious DiseaseCambridge, MassachusettsWe are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. Assist the Clinical Operations Lead(s) (COL) and/or Clinical Trial Manager(s) (CTM) in the day-to-day operational activities of assigned trials to ensure study objectives and timelines are met with quality, in compliance with applicable SOPs and regulatory guidelines.
Clinical Trial Associate, Clinical Operations, Therapeutics and Oncology ModernaTXClinical Trial Associate, Clinical Operations, Therapeutics and OncologyCambridge, MassachusettsThe Clinical Trial Associate (CTA) provides clinical trial coordination support to Project Teams for assigned clinical trial(s).This support includes tracking a wide range of key operational activities and maintenance of essential study documentation, including the electronic Trial Master File (eTMF). We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Clinical Trial Associate, Clinical Operations, Therapeutics and Oncology Moderna IncClinical Trial Associate, Clinical Operations, Therapeutics and OncologyCambridge, MA$74,000–$118,400 / yearThe Clinical Trial Associate (CTA) provides clinical trial coordination support to Project Teams for assigned clinical trial(s).This support includes tracking a wide range of key operational activities and maintenance of essential study documentation, including the electronic Trial Master File (eTMF). We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Clinical Trial Associate, Clinical Operations, Infectious Disease Moderna IncClinical Trial Associate, Clinical Operations, Infectious DiseaseCambridge, MA$74,000–$118,400 / yearWe are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. Assist the Clinical Operations Lead(s) (COL) and/or Clinical Trial Manager(s) (CTM) in the day-to-day operational activities of assigned trials to ensure study objectives and timelines are met with quality, in compliance with applicable SOPs and regulatory guidelines.
Global Head of Clinical Trial Management GaldermaGlobal Head of Clinical Trial ManagementBoston, MassachusettsLead a global team of internal/external Clinical Trial Managers (CTMs) responsible for the conduct of global, clinical trials across development phases and the Galderma pipeline. Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else.
Clinical Trial Associate Candel TherapeuticsClinical Trial AssociateNeedham, MAFull timeThis 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.
Clinical Trial Associate II Kailera TherapeuticsClinical Trial Associate IIWaltham, MassachusettsManages and regularly updates clinical trial tracking tools and systems that provide metrics and tracking of a clinical trial's progress, including participant recruitment, trial supplies, lab samples, and participant disposition. The Clinical Trial Associate II will provide support to the Director of Clinical Operations in the conduct of trials and may be responsible for managing startup activities, vendor communication, internal meetings, or other project activities, as assigned.
Clinical Trial Associate Treeline Biosciences IncClinical Trial AssociateWatertown, MA$68,883–$94,945 / yearUnsolicited resumes sent to Treeline Biosciences from recruiters do not constitute any type of relationship between the recruiter and Treeline Biosciences and do not obligate Treeline Biosciences in any way to pay fees should we hire from those resumes. To protect the interests of all parties involved, Treeline Biosciences will only accept resumes from a recruiter if an executed search agreement directed to the particular position or positions is in place at the start of the recruitment effort.
Clinical Trial Associate Candel Therapeutics IncClinical 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.
Clinical Trials Specialist - Surgery FIRST Program Lahey Hospital and Medical CenterClinical Trials Specialist - Surgery FIRST ProgramBoston, MA$60,000–$95,000 / yearThe FIRST program is an expansion of the existing research support infrastructure, facilitating the use of existing resources and assisting with tasks associated with study implementation, data collection and storage, biostatistics, and regulation guiding the conduct of research with human research participants. Implements process of protocol for various clinical trials; coordinates sponsor conducted initiated visit(s); assists in the execution of new IRB applications and processes annual reviews for the IRB committee with regard to consents.
Clinical Trials Specialist Lahey Hospital and Medical CenterClinical Trials SpecialistBoston, MA$60,000–$95,000 / yearThe Clinical Trials Specialist will help manage research projects including study coordination for an ongoing multicenter randomized controlled trial and managing multiple research projects using observational or real world datasets. The Cardio-Oncology and Heart Failure section combines the use of randomized clinical trials and real-world data with advanced statistical and epidemiological methods to answer questions related to the intersection between cancer and heart disease.
Clinical Trial Associate Verastem IncClinical Trial AssociateBoston, MA$86,000–$100,000 / yearCompany Profile: At Verastem Oncology, were advancing innovation and addressing the urgent needs of patients living with cancers driven by RAS/MAPK pathway mutations, a key driver of tumor growth and treatment resistance. The FDA approval of AVMAPKI FAKZYNJA CO-PACK delivered the first therapy specifically for women living with recurrent KRAS-mutated low-grade serous ovarian cancer, a rare cancer with significant unmet need.
Clinical Trials Monitor Lahey Hospital and Medical CenterClinical Trials MonitorBoston, MA$58,240–$90,002 / yearIncreases external and internal lab engagement by managing the lab''s social media following institutional guidelines, including the center website by creating content, updating news, publications, lab staff profiles, marketing of activities and events. Customer Service: Ability to provide a high level of customer service to patients, visitors, staff and external customers in a professional, service-oriented, respectful manner using skills in active listening and problem solving.
Clinical Trials Specialist Beth Israel Lahey HealthClinical Trials SpecialistBoston, MassachusettsThe Clinical Trials Specialist will help manage research projects including study coordination for an ongoing multicenter randomized controlled trial and managing multiple research projects using observational or real world datasets. The Cardio-Oncology and Heart Failure section combines the use of randomized clinical trials and real-world data with advanced statistical and epidemiological methods to answer questions related to the intersection between cancer and heart disease.
NewClinical Trial Associate Actalent IncClinical Trial AssociateWaltham, MA$40–$50 / hourThe Clinical Trial Assistant maintains high-quality documentation, supports site and vendor management, and helps ensure that all clinical trial activities align with regulatory requirements, internal procedures, and project timelines. The position involves frequent collaboration with internal cross-functional teams, external CROs, vendors, and investigational sites through virtual meetings, email, and other communication tools.
Senior Director, Clinical Trials Management Sumitomo Pharma America Holdings Inc (Inactive)Senior Director, Clinical Trials ManagementMarlborough, MA$236,400–$295,500 / yearThe Senior Director, Clinical Trials Management is responsible for operational leadership and oversight for vaccine clinical programs including operational strategy, clinical trial conduct, project planning, budget management, timelines, resource management, site management, monitoring, study management, vendor management, and project operational support. In collaboration with Clinical Operations Study Lead (as applicable), cross-functional teams and vendors on quality and compliance activities, ensuring continuous improvement in study conduct, proactively identifying and mitigating risks/issues to the study to ensure successful study conduct and reporting of study data.