Clinical Trial Associate Candel TherapeuticsClinical 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. Our Science: Advancing Cancer Immunotherapies Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses.
Associate Director/Director, Pre-Clinical Program & Alliance Management Kiniksa Pharmaceuticals CorpAssociate Director/Director, Pre-Clinical Program & Alliance ManagementLexington, MA$191,000–$242,000 / yearThis individual will serve as the central operational hub for one or more pre-clinical assets, coordinating cross-functional activities across research, CMC, nonclinical safety/toxicology, translational, regulatory, and program leadership, while also managing day-to-day interactions with external partners, CROs, and collaborators. Kiniksa is seeking a highly organized and execution-oriented Associate Director / Director, Pre-Clinical Program and Alliance Management to drive the operational planning, integration, and delivery of pre-clinical programs from candidate nomination through successful IND filing and acceptance.
Associate Director, Clinical Program Quality and Excellence (Oncology) 3316 Takeda Development Center AmericasAssociate Director, Clinical Program Quality and Excellence (Oncology)MassachusettsProvides quality assurance oversight of the global clinical research programs in Research and Development (R&D), Plasma Derived Therapy (PDT), Vaccines Business Unit (VBU), Oncology Business Unit (OBU) and Global Medical Marketed Products Development (MPD) with the overall goal of inspection readiness. Lead investigations into significant quality issues, scientific misconduct and serious breach of GCP; facilitate identification of root cause and development of appropriate corrective and preventive actions; track actions and confirm effectiveness; ensure reporting of potential or confirmed violations to regulatory authorities.
Associate Director Clinical Scientist, Immunology Cell Therapy AstraZeneca PlcAssociate Director Clinical Scientist, Immunology Cell TherapyCambridge, MA$142,171.20–$213,256.80 / yearStudy level: Serving as the clinical science resource for assigned studies (and in some instances as the Study Clinical Lead); supporting/leading development of Clinical Study Protocols (CSPs), informed consent forms (ICFs), and electronic data capture (EDC) database specifications in line with the approved CDP and target product profile; supporting ongoing clinical data review and interpretation at study and program level with input from the study/program physician; contributing to development of quality metrics and data review plans for assigned studies; support and contribute to medical monitoring of trials; supporting the compilation and interpretation of data for dose‑escalation/safety review committees; supporting protocol amendments and other strategic documents; and supporting review of the Clinical Study Report. ESCR and external engagement: Co‑leading/supporting ESCR strategy and implementation for the program; serving as the interface between the GPT and external clinical research; supporting investigator/site relationships for site selection and study start‑up; co‑leading/supporting clinical proposal reviews, protocol reviews and scientific oversight for academic basket/umbrella and ESCR studies; identifying and managing ESCR portfolio risks and escalating quality issues through appropriate channels; supporting representation of the project internally and externally with key experts and partners and contributing to alliance development.
Associate Director Clinical Scientist Immunology Cell Therapy AstraZeneca PlcAssociate Director Clinical Scientist Immunology Cell TherapyCambridge, MA$142,171.20–$213,256.80 / yearStudy level: Serving as the clinical science resource for assigned studies (and in some instances as the Study Clinical Lead); supporting/leading development of Clinical Study Protocols (CSPs), informed consent forms (ICFs), and electronic data capture (EDC) database specifications in line with the approved CDP and target product profile; supporting ongoing clinical data review and interpretation at study and program level with input from the study/program physician; contributing to development of quality metrics and data review plans for assigned studies; support and contribute to medical monitoring of trials; supporting the compilation and interpretation of data for dose‑escalation/safety review committees; supporting protocol amendments and other strategic documents; and supporting review of the Clinical Study Report. ESCR and external engagement: Co‑leading/supporting ESCR strategy and implementation for the program; serving as the interface between the GPT and external clinical research; supporting investigator/site relationships for site selection and study start‑up; co‑leading/supporting clinical proposal reviews, protocol reviews and scientific oversight for academic basket/umbrella and ESCR studies; identifying and managing ESCR portfolio risks and escalating quality issues through appropriate channels; supporting representation of the project internally and externally with key experts and partners and contributing to alliance development.
Associate Director, Clinical Data Programmer Amylyx PharmaceuticalsAssociate Director, Clinical Data ProgrammerCambridge, MARemote$188,000–$211,000 / yearThis individual will work collaboratively cross-functionally to provide hands-on data management support, programming support and technical leadership to develop, maintain, validate the clinical database, and run computer programs that access, visualize, and report clinical trial data, in accordance with various clinical plans, ICH guidelines, and applicable regulatory requirements. You will be expected to travel to our corporate location in Cambridge, MA several times a year and attend other company-related events as necessary and requested, which may include travel by air, driving or public transportation.
NewAssociate Director, Clinical Development Project Manager - Oncology GSK plcAssociate Director, Clinical Development Project Manager - OncologyWaltham, MARemote$139,425–$232,375 / yearCommunication, Cross-Departmental Collaboration, Decision Making, Financial Acumen, Innovation, Leadership, Project Controls, Project Management, Project Management Governance, Project Planning, Project Tracking, Risk Management, Stakeholder Engagement, Stakeholder Management, Strategic Leadership. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success.
Associate Director, Clinical Data Management X4 Pharmaceuticals IncAssociate Director, Clinical Data ManagementBoston, MAThe Associate Director will oversee CRO partners and vendors, drive data quality and inspection readiness, support regulatory submissions, and ensure the timely delivery of high-quality clinical trial data. Does it excite you to be a part of a patient-focused company developing potential new treatments that could dramatically improve the lives of patients with limited to no current treatment options?
Senior Research Associate, Oligonucleotide Chemistry Tessera TherapeuticsSenior Research Associate, Oligonucleotide ChemistrySomerville, MA$90,000–$108,000 / yearCompany Summary: Tessera Therapeutics is pioneering Gene Writing- a new biotechnology designed to offer scientists and clinicians the ability to write small and large therapeutic messages into the genome, thereby curing diseases at their source. The submission of unsolicited resumes by recruitment or staffing agencies to Tessera Therapeutics or its employees is strictly prohibited unless contacted directly by Tessera Therapeutics' internal Talent Acquisition team.
NewResearch Associate II, NGS Flagship Pioneering, Inc.Research Associate II, NGSCambridge, MA USA$74,000–$94,500 / yearThe company’s initial therapeutic programs are designed to restore full-length protein production in diseases caused by premature termination codons (PTCs), collectively referred to as Stop Codon Disease, which affect approximately 10% of people with a rare genetic disease. Alltrna’s NGS pipeline is central to company initiatives, and this role will collaborate closely with a cross-functional team of scientists in molecular biology, computational biology, and lab automation.
Research Associate/Engineer I, CMC Development (2027 Rotation Program) Moderna IncResearch Associate/Engineer I, CMC Development (2027 Rotation Program)Norwood, MA$63,200–$100,900 / 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. Bachelors or Masters Degree in Chemical Engineering, Biochemical Engineering, Bioengineering, Biomolecular Engineering, Chemistry, Biochemistry, Biomedical Engineering, Biophysics, Biostatistics, Biotechnology, Mathematics, Molecular Biology, Pharmaceutical Science, Statistics, or a related field preferred.
Associate Director, Clinical Supplies Project Manager ModernaTXAssociate Director, Clinical Supplies Project ManagerCambridge, 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. The scope includes the operational planning and strategy required to execute end-to-end supply management, including demand planning, label development, packaging/labeling, distribution, IRT UAT/supply management, temperature excursions, and site activations.
Associate Director, Quantitative Clinical Pharmacology (QCP) Lead 3316 Takeda Development Center AmericasAssociate Director, Quantitative Clinical Pharmacology (QCP) LeadBoston, Massachusetts$154,400–$242,550 / yearAdvanced knowledge of pharmaceutical industry, overall drug development process with expertise in the cross-functional interfaces with key partners such as Pharmacometrics, Statistics, Drug Safety, Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/Device, and Global Regulatory Affairs. These scientists (from quantitative clinical pharmacology, statistics, programming, outcomes research and epidemiology, patient safety & pharmacovigilance, digital strategy, library sciences and data architecture/governance) bring their expertise to our global program teams and reimagine our disciplines.
Associate Director, Scientific Communications Lead, Solid Tumors, Global Medical Affairs Oncology 3312 Takeda Pharmaceuticals AmericaAssociate Director, Scientific Communications Lead, Solid Tumors, Global Medical Affairs OncologyCambridge, Massachusetts$169,400–$266,200 / yearYou will develop and implement strategic publications and scientific communications plans in coordination with relevant cross-functional teams (including members of medical affairs, clinical development, and outcomes research; global, regional, or local); leads the publications planning team; manages the development of scientific publications for external audiences and scientific communications materials such as slide decks, NCCN or pathway submissions, animations, and digital amplification of data; manages vendors, freelancers, and available contractors, writers, and editors in the execution of publication and scientific communications tactics; and manages annual budget planning for each assigned program(s). This individual will work closely with the Scientific Communications Group Lead, Solid Tumors to optimize department resources and evaluate trends in medical publications, and lead and/or participate in the development and review of publications SOPs and Work Practices, where appropriate, to ensure delivery of high-quality medical publications in a timely and compliant manner across programs.
Statistics Leader / Associate Director of Statistics GSK plcStatistics Leader / Associate Director of StatisticsWaltham, MA$150,150–$250,250 / yearThe Oncology Clinical Development Statistics group is seeking exceptionally talented Statisticians to provide end-to-end statistical leadership across oncology evidence generation-from early development through registration and lifecycle support-using innovative trial designs and modern statistical methods (including simulation, interim strategies, Bayesian approaches, and external/real-world data) to inform key development decisions. Offers are typically made within the advertised range based on the candidate's skills, experience and qualifications, with the upper end generally reserved for highly experienced candidates or other exceptional circumstances aligned with these criteria.
Associate Director or Director, Biostatistics Kymera TherapeuticsAssociate Director or Director, BiostatisticsWatertown, MA$160,000–$275,000 / 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. As the Study/Program Lead Statistician, you will spearhead the statistical efforts of a clinical study/program playing a key role in the clinical development plan, regulatory submissions, and overall data strategy.
Registered Nurse (RN) - Oncology Clinical Research, 40 hours/week, day shift Lahey Hospital and Medical CenterRegistered Nurse (RN) - Oncology Clinical Research, 40 hours/week, day shiftBeverly, MA$37–$84.71 / hourCollaborates with local hematology/oncology physicians, nurses, pharmacy, office support staff as well as other research members across the BILH network t stay up to date with new and ongoing oncology research and operations. Provides both supportive and direct patient care to those who enroll to a trial including scheduling collaboration, symptom monitoring and maintenance, and follow up care/monitoring.
Associate Director, Data Architect Amylyx Pharmaceuticals IncAssociate Director, Data ArchitectCambridge, MARemote$190,000–$206,000 / yearThis individual will play a key role in building a scalable, modern data ecosystem centered on Snowflake, enabling trusted, high-quality data across Commercial, Medical Affairs, Patient Services, Finance, R&D, Quality, and Corporate functions. Design and oversee integration of key commercial data sources including: CRM, Specialty Pharmacy, Specialty Distributor, Patient Services, Claims and Prescription Data, Formulary and Market Access Data, Customer Master Data, etc.
Associate Director, International GVP Compliance 3316 Takeda Development Center AmericasAssociate Director, International GVP ComplianceBoston, Massachusetts$154,400–$242,550 / yearThe role is responsible for strengthening GVP Quality System execution, driving inspection readiness, leading compliance investigations and CAPA activities, identifying emerging compliance risks, and supporting continuous improvement initiatives that protect patient safety and maintain regulatory integrity. 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.
Associate Director, U.S. Communications, Rare Blood Disorders SanofiAssociate Director, U.S. Communications, Rare Blood DisordersCambridge, MA$123.75–$178.75 / hourThe Lead is responsible for planning and managing external and internal communications for the RBD franchise in the U.S. by driving communications for marketed products treating serious rare blood disorders such as hemophilia, acquired thrombotic thrombocytopenic purpura (aTTP)/immune-mediated thrombotic thrombocytopenic purpura (iTTP), and immune thrombocytopenia (ITP), as well as a potential assets in late-stage clinical development. Provide communications counsel and strategic input to support the RBD business, including currently marketed products for hemophilia, aTTP/iTTP, and ITP, as well as late-stage pipeline assets in clinical development; drive execution of communications programs that deliver measurable business results.