Clinical Research Nurse, Pediatrics Boston Medical CenterClinical Research Nurse, PediatricsBoston, MA$34.38–$50 / hourKey responsibilities include maintaining a leadership role in the prenatal, pediatric HIV and research activities of the section of pediatric infectious diseases integrating clinical care, patient education and access to research protocols appropriate for the BMC population. The major responsibilities of this position will be maintaining a leadership role in the prenatal, pediatric HIV and research activities of the section of pediatric infectious diseases integrating clinical care, patient education and access to research protocols appropriate for the BMC population.
Associate Director, Clinical Quality Compliance Stoke Therapeutics IncAssociate Director, Clinical Quality ComplianceBedford, MA$192,000–$215,000 / yearThis person will support Stoke's clinical study teams towards ensuring compliance with global regulations (e.g., FDA, EMA, etc.) and will be required to contribute to developing the right strategies for the design and execution of all Stoke clinical and bioanalytical studies. This person will be responsible for establishing Stokes inspections management program for GCP inspections and expected to be influential towards maturing Stoke's quality culture and help reach a sustained state of inspection readiness.
NewAssociate Director, Clinical Study Quality Lead (Hybrid) Vertex PharmaceuticalsAssociate Director, Clinical Study Quality Lead (Hybrid)Boston, MassachusettsOverall, the SQL is responsible for the development and execution of audit/quality plans, accurately identifying and communicating compliance risks and overseeing action plans to mitigate risks, real-time study inspection readiness oversight, and collaboratively identifying and driving inspection preparedness strategies and activities. Provides strategic, risk-based GCP quality compliance oversight of studies within assigned disease areas to drive compliance with regulatory requirements to ensure the protection of participants’ safety, rights, and well-being as well as the integrity and credibility of study data generated.
NewClinical Development Medical Director-Nephrology Vertex PharmaceuticalsClinical Development Medical Director-NephrologyBoston, MassachusettsParticipates in the preparation of regulatory documents in support of regulatory submissions, including clinical section of INDs and CTAs, IND safety reports and annual reports for assigned trials, responses to regulatory authorities and Ethics Committees/IRBs, and other documents as appropriate. Provides scientific and clinical input to study-related documents and analysis plans including informed consent forms, clinical research forms, statistical analysis plans, clinical pharmacology analysis plans, and clinical study reports.
Research Assistant I - Osterweil Lab Boston Children's HospitalResearch Assistant I - Osterweil LabBoston, MAThe candidate will contribute to projects using advanced molecular and cellular techniques (scRNA-seq, TRAP-seq), electrophysiology, and 2-photon GCAMP calcium imaging, and acquire the skills needed to perform and analyze experiments. The individual will join a fast-paced translational team that uses human brain slice and rodent models to study neurological disease ( www.osterlab.org/ ).
Staff Scientist Boston Children's HospitalStaff ScientistBrookline, MA$83,241.60–$133,192.80 / yearWorking with the Principal Investigator (PI) provides scientific expertise and leads and guides a research team in the development of original scientific research at BCH. May manage and/or advise lab personnel and have latitude in decision-making, including a role in the management of departmental or institutional cores.
Managing Consultant, Health & Safety (Biosafety Focus) ERM International Group LtdManaging Consultant, Health & Safety (Biosafety Focus)Boston, MA$103,872–$130,886 / yearThis is an opportunity to influence how leading biotechnology, pharmaceutical, research, and high-tech organizations design and run their biosafety and health & safety programs-moving beyond compliance toward resilient, high-performing systems that enable innovation while protecting people and operations. Who We Are: As the largest global pure play sustainability consultancy, we partner with the world's leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
NewAcademic Partnerships Director Beacon BiosignalsAcademic Partnerships DirectorBoston, MassachusettsRemoteBeacon Biosignals is seeking a scientifically and clinically credentialed, relationship-driven Academic Partnerships Director to grow adoption of the Beacon Platform, including the research use of its medical devices, within academic and research institutions. As such, we’re always seeking new contributors whose work demonstrates an avid curiosity, a bias towards simplicity, an eye for composability, a self-service mindset, and, most of all, a deep empathy towards colleagues, stakeholders, users, and patients.
Director, Drug Safety & Pharmacovigilance (Inflammation & Oncology) Monte Rosa Therapeutics, IncDirector, Drug Safety & Pharmacovigilance (Inflammation & Oncology)Boston, MassachusettsFull timeThis role is responsible for establishing and executing global safety strategy across early‑ and mid‑stage clinical programs, with particular focus on immune‑mediated toxicities, oncology risk management, and complex benefit–risk assessment. Overview: The Director of Drug Safety & Pharmacovigilance provides strategic and hands‑on leadership for pharmacovigilance activities supporting a clinical‑stage biotech pipeline in inflammatory and oncology diseases .
Clinical Development Senior Medical Director-Neurology Vertex Pharmaceuticals, IncClinical Development Senior Medical Director-NeurologyBoston, MA$280,600–$420,800 / yearGeneral Summary: The Senior Medical Director will define the clinical development strategy of an asset, work with cross-functional multidisciplinary teams to define overall asset strategy as well as clinical trials strategy, design and execution, and may serve as the Medical Lead for clinical trials that will be conducted with these compounds. Serves on cross-functional study teams for assigned trials, working with other team members to achieve efficient, high-quality study execution, and data analysis.
Clinical Development Medical Director- Pain Vertex Pharmaceuticals, IncClinical Development Medical Director- PainBoston, MA$240,000–$360,000 / yearGeneral Summary: The Clinical Development Medical Director will serve as the Medical Lead for Vertex clinical trials, working with cross-functional multidisciplinary study teams on clinical trial strategy, design and execution and serving as the Medical Monitor responsible for monitoring the safety of enrolled subjects on assigned trials. Provides scientific and clinical input to study-related documents and analysis plans including Informed consent forms (ICF), clinical research forms (CRF), statistical analysis plans (SAP), clinical pharmacology analysis plans (CPAP), and clinical study reports (CSR).
Senior Medical Science Liaison - Pain (Georgia) Vertex Pharmaceuticals IncSenior Medical Science Liaison - Pain (Georgia)Boston, MA$171,300–$256,900 / yearThe Sr MSL serves as a scientific liaison to the medical/academic community and is responsible for establishing and maintaining relationships with (Allied) Health Care Providers/Professionals (HCPs) and other key stakeholders involved in healthcare decision making to ensure the appropriate dissemination of clinical, scientific, and health economic data with respect to pain and Vertex's compounds in a timely, ethical, and stakeholder-focused manner. Develops and fosters effective and trusting relationships with Thought Leaders and identifies and engages other appropriate (allied) HCPs and other stakeholders involved in clinical practice decision making with regards to managing conditions associated with pain, resulting in scientific engagement with a large network of stakeholders involved in affecting care of patients experiencing pain.
Senior Medical Director, Clinical Development- POVE Vertex PharmaceuticalsSenior Medical Director, Clinical Development- POVEBoston, Massachusetts$280,600–$420,800 / yearThe Senior Medical Director will define the clinical development strategy of povetacicept in primary membranous nephropathy, work with cross-functional multidisciplinary teams to define overall asset strategy as well as clinical trials strategy, design and execution, and may serve as the Medical Lead for clinical trials that will be conducted with these compounds. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.
Senior Medical Director, Clinical Development- Pove Vertex Pharmaceuticals, IncSenior Medical Director, Clinical Development- PoveBoston, MA$280,600–$420,800 / yearGeneral Summary: The Senior Medical Director will define the clinical development strategy of povetacicept in primary membranous nephropathy, work with cross-functional multidisciplinary teams to define overall asset strategy as well as clinical trials strategy, design and execution, and may serve as the Medical Lead for clinical trials that will be conducted with these compounds. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.
Clinical Development Associate Medical Director- Pain Vertex Pharmaceuticals, IncClinical Development Associate Medical Director- PainBoston, MA$204,000–$306,000 / yearParticipates in the preparation of regulatory documents in support of regulatory submissions, including clinical section of INDs and CTAs, IND safety reports and annual reports for assigned trials, responses to regulatory authorities and Ethics Committees/IRBs, and other documents as appropriate. Provides scientific and clinical input to study-related documents and analysis plans including informed consent forms, clinical research forms, statistical analysis plans, clinical pharmacology analysis plans, and clinical study reports.
Senior Director, National Field Medical Lead Entrada Therapeutics Inc.Senior Director, National Field Medical LeadBoston, MARemote$277,000–$317,000 / 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. Proven experience in working collaboratively and cross functionally across the enterprise of field medical teams, clinical development, commercial, sales, market access and other key functions and demonstrated ability to inform and shape company/product strategy.
Writer/Editor Consultant - Institutional History Book Project ForsythWriter/Editor Consultant - Institutional History Book ProjectSomerville, MAThe consultant will collaborate with Institute leadership, Communications, and Senior Investigator to ensure the manuscript accurately reflects Forsyth's history, scientific contributions, and lasting impact on the field. The selected consultant will help synthesize, organize, write, and edit these materials into a compelling and cohesive narrative suitable for publication.
Clinical Study Quality Lead, Associate Director Vertex Pharmaceuticals, IncClinical Study Quality Lead, Associate DirectorBoston, MA$160,600–$240,800 / yearOverall, the SQL is responsible for the development and execution of audit/quality plans, accurately identifying and communicating compliance risks and overseeing action plans to mitigate risks, real-time study inspection readiness oversight, and collaboratively identifying and driving inspection preparedness strategies and activities. Provides strategic, risk-based GCP quality compliance oversight of studies within assigned disease areas to drive compliance with regulatory requirements to ensure the protection of participants' safety, rights, and well-being as well as the integrity and credibility of study data generated.
Medical Writing Science Senior Manager (Hybrid) Vertex PharmaceuticalsMedical Writing Science Senior Manager (Hybrid)Boston, Massachusetts$137,200–$205,800 / yearAuthors complex clinical regulatory documents (e.g., clinical study protocols, clinical study reports, investigator’s brochures, documents to support meetings with regulatory agencies, and sections of marketing authorization applications) in partnership with key stakeholders. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.
Medical Writing Manager (Hybrid) Vertex PharmaceuticalsMedical Writing Manager (Hybrid)Boston, Massachusetts$120,200–$180,400 / yearAuthors moderately complex clinical regulatory documents (e.g., including clinical study protocols, clinical study reports, investigator’s brochures, and sections of regulatory submissions) in partnership with key cross-functional stakeholders. The Medical Writing Science Manager is responsible for preparing moderately complex clinical and regulatory documents and represents Medical Writing Science as a cross-functional team member at clinical study level activities.