Associate Director, PV Scientist — Safety & Signal Lead
Tango Therapeutics, Inc
Tango Therapeutics, Inc. is seeking an Associate Director, Pharmacovigilance Scientist to lead safety surveillance and deliver regulatory safety reporting across product lifecycles. You will partner with cross‑functional teams to assess benefit‑risk and ensure compliance with global PV standards. Responsibilities include DSUR/PSUR preparation, signal detection, and contributing to clinical trial documents, while advancing a scalable pharmacovigilance program for oncology assets. #J-18808-Ljbffr Tango Therapeutics, Inc
- Scorpion Therapeutics seeks an Associate Director, Pharmacovigilance Scientist to lead safety evaluation across clinical development... ...SAE review, safety analyses, signal management, regulatory documentation, and collaboration with PV vendors. #J-18808-Ljbffr Scorpion...Suggested
- Biogen is looking for an Associate Director for the Safety Surveillance and Aggregate Reports group in Cambridge... ..., MA. This hybrid role involves leading safety oversight and managing a team... ..., experience with safety signal management, and the ability to articulate...Suggested
$172k - $237k
About This Role As the Associate Director for the Safety Surveillance and Aggregate Reports group, you will... ....What You’ll Do Serve as the lead PV Scientist for a specific product or group of... ...direction and scientific oversight.Oversee signal detection and management activities...SuggestedFull timeTemporary workWork at officeLocal area- Tango Therapeutics in Boston seeks Associate Director, Pharmacovigilance Scientist to lead ongoing safety surveillance, oversee signal detection, author DSURs and PSURs, and manage regulatory... ...to ensure alignment with FDA, ICH and EU PV guidelines, maintain RSI accuracy, drive...Suggested
- AVEO is seeking a PV Scientist in Boston, Massachusetts to support clinical safety through safety surveillance and regulatory reporting. This role involves developing signal management tools and collaborating with cross-functional teams to ensure compliance with pharmacovigilance...SuggestedPart time3 days per week
$126k - $190k
The Associate Director, Safety Scientist plays a pivotal role within Global Patient Safety... ...will be responsible for:Leading safety data reviews and analyses... .../tracking of all signal analysis resultsLeading the... ...and reputational impact of PV actionsThe duties of this...Full timeTemporary workWork at officeLocal area$161.6k - $242.4k
..., Massachusetts.SummaryThe Associate Director, Pharmacovigilance Scientist, reporting to the Senior Director, Drug Safety, plays a pivotal role, partnering... ...data, manage adverse event signals and author regulatory... ...current FDA, ICH guidelines, EU PV regulations and other PV...Flexible hours- Position Summary: The Associate Director, Pharmacovigilance Scientist supports safety evaluation and pharmacovigilance activities... ...to safety topic reviews, signal evaluations, aggregate safety analyses... ...risk language. Collaborate with PV vendors/CROs for quality case processing...
$68 - $80 per hour
...on experiencePosition Summary The PV Aggregate Reports Scientist is part of the Safety Surveillance and Aggregate (SSA) Reports... ...Aggregate Report Management: Lead and conduct all aspects of... ...consistency in aggregate reporting, signal management, clinical trial safety...Local areaWorldwide- ...Job Description Job Description PV Scientist, Contractor, Safety Risk Management 6 Months Remote Summary... ...Responsibilities Works closely with the safety lead physician to analyze potential safety issues, including signal detection, signal evaluation and signal...Permanent employmentContract workFor contractorsRemote work
- IntelliPro seeks a PV Drug Safety Consultant to join our Hybrid Cambridge team. The role focuses on managing PSUR/DSUR/PADER and local reports across global safety programs, ensuring high-quality PV documentation. You will collaborate with Safety, Clinical Development,...Local area
$65 - $77 per hour
job summary: The PV Aggregate Reports Scientist is part of the Safety Surveillance and Aggregate (SSA) Reports team and... ...: Aggregate Report Management: Lead and conduct all aspects of... ...consistency in aggregate reporting, signal management, clinical trial safety...Hourly payContract workTemporary workWork experience placementLocal areaWorldwide$70 - $78 per hour
Pride Health is supporting a leading biotechnology organization with a hybrid contract opening for a PV Aggregate Reports Scientist within the Safety Surveillance and Aggregate (SSA) Reports... ...Quality, and external vendors. Support signal management, clinical trial safety...Contract workLocal area$184k - $200k
...Associate Director, Pharmacovigilance Scientist Location: Remote or, Hybrid, Needham... ...Phase 3 results for our lead candidate, it's an... ...support the ongoing safety evaluation and... ...implement a robust signal management process and... ...Collaborate with PV vendors and CROs to...Remote work- CRISPR Therapeutics is seeking a Senior Specialist, Drug Safety to support ICSR processing and maintain high-quality safety cases. Reporting to PV Ops, you will reconcile safety data and ensure timely submissions to regulators, CROs and partners. You will develop data entry...
- ...Therapeutics, Inc. is seeking an Associate Director, Pharmacovigilance Scientist to advance safety evaluation across clinical... ...will oversee SAE reviews, support signal management, and collaborate with... ...teams. The role requires extensive PV experience, strong regulatory knowledge...Remote job
$142k - $213k
Are you a scientist with a passion for clinical drug development and... ...by patient outcomes. The Associate Director, Clinical Scientist is a member... ...the Global Clinical Program Lead (GCPL), who leads the... ...tables, laboratory and other safety parameters, and coded terms...Full timeTemporary work- About the Opportunity A biotechnology organization focused on developing innovative therapeutic solutions is seeking an experienced Clinical Science professional to support the advancement of its clinical development programs. This individual will play a key role in guiding...
- ...Department at Alnylam is seeking a passionate and creative physician-scientist to join the Translational Research Group to play a key role in... ..., and Clinical Research teams to drive programs from lead target identification through early-stage (Ph1/2) clinical trials...Full timeTemporary workLocal areaFlexible hours
$160k - $275k
...focused on building an industry-leading pipeline of oral small... ...as the study level Clinical Scientist in immunology, with a focus on... ...meetings, vendor meetings, and data/safety monitoring committees.Support... ..., collaborating with medical directors, regulatory affairs,...- Pride Health is seeking a PV Aggregate Reports Scientist for a hybrid contract in Cambridge, MA. The role focuses on leading the preparation of PSURs, DSURs, PADERs, and other aggregate safety reports within the SSA team. The candidate should have at least 5 years of Pharmacovigilance...Contract work
$135k - $205k
...is seeking a tenured, equity-minded leader who can advance our college mission, in leading the Institute for Community Inclusion (ICI). The Director will also hold a qualified Associate/Full Professor position in an academic unit within the College of Education and Human...Contract workWork at officeLocal area- ...based biotech recruitment partner, is seeking a Senior Scientist in Toxicology to shape the preclinical safety strategy for oligonucleotide programs across... ...collaborating with cross-functional teams. The role requires leading GLP/non-GLP toxicology studies, directing CROs, and...
$184k - $200k
...Title: Associate Director, Pharmacovigilance Scientist Location: Remote or, Hybrid,... ...Phase 3 results for our lead candidate, it’s an... ...support the ongoing safety evaluation and pharmacovigilance... ...implement a robust signal management process... ...• Collaborate with PV vendors and CROs to...Full timeRemote work- A leading biotechnology company in Cambridge, MA is seeking an Associate Director for the Safety Surveillance and Aggregate Reports group. The role involves overseeing product safety, leading signal management activities, and collaborating with various teams. Candidates...
- ...decade ago, CRISPR Therapeutics is a leading biopharmaceutical company focused on... ...Therapeutics is searching for an Associate Director, Clinical Scientist to provide scientific input for early... ...initial review of clinical trial data (safety and efficacy), including assessing...Remote work
- ...Associate Director, Clinical Scientist How you'll make an impact: Serve as the study lead Clinical Scientist in immunology, actively participating in program team meetings, scientific advisory boards, and data/safety monitoring committees. Support the design...
$75 - $80 per hour
Job Title : Drug Safety Consultant II/Pharmacovigilance Scientist Location : Cambridge, MA — Hybrid... ...reports Experience with safety signal detection, evaluation,... ...Knowledge of global PV regulations and clinical/... ...sets us apart. We continue leading global talent solutions with...Work experience placementLocal area$187k - $281k
...The Director, Safety Scientist serves as a key leader within Global Patient Safety... ...the portfolio through: Leading the scientific evaluation and... ...compliance and adherence to PV regulations for the assigned... ...documentation/tracking of all signal analysis results Leading...Temporary workLocal area$131.2k - $196.8k
...Job Title: Associate Principal Scientist Location: Waltham, MA The Rare Cancer... ...Scientist /Associate Director will provide scientific leadership... ...Key Responsibilities ~ Lead and contribute to... ...assess efficacy, potency, and safety signals, and inform go/no-go program...Hourly payTemporary work
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