Senior Drug Safety Specialist

1 week ago


Cambridge, United States Integrated Resources, Inc Full time

Job Title: Senior Drug Safety Specialist

Location: Cambridge, MA

Duration: 8+ Months

Job Description:

Duties:

· Reporting to the Associate Director, Drug Safety and Pharmacovigilance Compliance and Operations, you will play a pivotal role in drug safety activities, supporting records management and compliance across the clinical development and marketing programs. You will be a key contributor to the day-to-day operational activities of the department, ensuring that performed tasks comply with DSPV SOP’s, policies, industry standards, and applicable regulations.

· What will you do?

· Identifies and supports the DSPV team with document management activities (e.g., electronic Trial Master File, Veeva), including maintaining electronic files internally, and collaborate cross- functionally with Client teams, CRO’s and vendors.

· Contribute to the quality management Drug Safety system including: ensuring department standards are met, training requirements, monitoring performance, implementing continuous improvement actions and documentation practices.

· Participates in the daily management and execution of compliance activities.

· Assists with document development requirements are identified and aligned to overall strategic objects.

· Assists with monitoring DSPV compliance with regulations, PV agreements and internal SOPs.

· Function on supporting teams for projects in support of DSPV results.

· Supports sponsor oversight of AE/SAE processing by outsourced vendors, including the review and monitoring of compliance through various monitoring reports and other oversight activities and ensures the implementation of effective corrective and preventative action plans.

· Assist with working with DSPV and QA departments to maintain a state of high PV inspection readiness across all regions/countries.

· Participates in regulatory inspections and company audits including FDA/MHRA/EMA PV inspections; assists with prepares responses to audit findings that concern the DSPV department.

Education:

· Bachelor’s degree in nursing, pharmacy, or other health care related field.

Languages:

· English( Speak, Read, Write )


  • Associate Director Drug Safety Scientist

    Found in: Appcast Linkedin GBL C2 - 5 days ago


    Cambridge, United States Pharma People Full time

    About the jobOur client is a clinical stage Biotechnology company based in Massachusetts looking to bring on an Associate Director Drug Safety Scientists. This role is a safety expert position contributing to the global safety strategy and overall safety profile for the assigned products throughout lifecycle as well as their post-marketed products....

  • Medical Director, Drug Safety

    Found in: Resume Library US A2 - 2 weeks ago


    Cambridge, Massachusetts, United States Biogen Full time

    Job Description About This Role The Medical Director, Drug Safety is responsible for global pharmacovigilance for marketed and/or investigational products, including review and analysis of safety data from post-marketing sources and from clinical trials, the identification, and investigation of safety signals, management of benefit-risk profile for...

  • Senior Safety Associate

    Found in: Appcast Linkedin GBL C2 - 3 days ago


    Cambridge, United States Randstad Life Sciences US Full time

    Sabr Associate III / Senior Safety Associate III6 Month Initial ContractCambridge, MA (Hybrid possible)Max PR: $57.58MUST HAVE - Willingness to work ONSITE in Cambridge, MA +BS in Nursing, Pharmacy, Healthcare or LifesciencesDirect End-to-End Case Processing experience (data entry and quality review) Experience with both Clinical Trial and Post-marketing...


  • Cambridge, United States Randstad Life Sciences US Full time

    Sabr Associate III / Senior Safety Associate III6 Month Initial ContractCambridge, MA (Hybrid possible)Max PR: $57.58MUST HAVE - Willingness to work ONSITE in Cambridge, MA +BS in Nursing, Pharmacy, Healthcare or LifesciencesDirect End-to-End Case Processing experience (data entry and quality review) Experience with both Clinical Trial and Post-marketing...

  • Senior Safety Associate

    Found in: Appcast US C2 - 4 days ago


    Cambridge, United States Randstad Life Sciences US Full time

    Sabr Associate III / Senior Safety Associate III6 Month Initial ContractCambridge, MA (Hybrid possible)Max PR: $57.58MUST HAVE - Willingness to work ONSITE in Cambridge, MA +BS in Nursing, Pharmacy, Healthcare or LifesciencesDirect End-to-End Case Processing experience (data entry and quality review) Experience with both Clinical Trial and Post-marketing...

  • Senior Safety Associate

    Found in: Appcast US C2 - 24 hours ago


    Cambridge, United States Randstad Life Sciences US Full time

    Sabr Associate III / Senior Safety Associate III6 Month Initial ContractCambridge, MA (Hybrid possible)Max PR: $57.58MUST HAVE - Able to work onsite Cambridge (Flexible with how often 1x/wk, 1x/month) BS in Nursing, Pharmacy, Healthcare or LifesciencesDirect End-to-End Case Processing experience (data entry and quality review) Experience with both Clinical...

  • Senior Safety Associate

    Found in: Appcast Linkedin GBL C2 - 1 day ago


    Cambridge, United States Randstad Life Sciences US Full time

    Sabr Associate III / Senior Safety Associate III6 Month Initial ContractCambridge, MA (Hybrid possible)Max PR: $57.58MUST HAVE - Able to work onsite Cambridge (Flexible with how often 1x/wk, 1x/month) BS in Nursing, Pharmacy, Healthcare or LifesciencesDirect End-to-End Case Processing experience (data entry and quality review) Experience with both Clinical...


  • Cambridge, United States Randstad Life Sciences US Full time

    Sabr Associate III / Senior Safety Associate III6 Month Initial ContractCambridge, MA (Hybrid possible)Max PR: $57.58MUST HAVE - Able to work onsite Cambridge (Flexible with how often 1x/wk, 1x/month) BS in Nursing, Pharmacy, Healthcare or LifesciencesDirect End-to-End Case Processing experience (data entry and quality review) Experience with both Clinical...


  • Cambridge, United States QurAlis Full time

    ABOUT THE COMPANY QurAlis is a clinical-stage biotechnology company developing breakthrough precision medicines for amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases with genetically validated targets.  QurAlis is trailblazing the path to conquering amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases with...

  • Director of Drug Substance Manufacturing

    Found in: Appcast US C2 - 1 week ago


    Cambridge, United States QurAlis Full time

    ABOUT THE COMPANY QurAlis is a clinical-stage biotechnology company developing breakthrough precision medicines for amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases with genetically validated targets.  QurAlis is trailblazing the path to conquering amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases with...

  • Director of Drug Substance Manufacturing

    Found in: Appcast Linkedin GBL C2 - 2 weeks ago


    Cambridge, United States QurAlis Full time

    ABOUT THE COMPANY QurAlis is a clinical-stage biotechnology company developing breakthrough precision medicines for amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases with genetically validated targets.  QurAlis is trailblazing the path to conquering amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases with...

  • Environmental Health Safety Specialist

    Found in: Appcast US C2 - 1 week ago


    Cambridge, United States Randstad Life Sciences US Full time

    Immediate opportunity for an Environmental Health & Safety Specialist II to work with multi-national pharmaceutical company dedicated to pharmaceutical research and vaccine development. The HSE Associate Level Service Provider serves an important and highly visible role helping to ensure that site HSE Management System (HSE-MS) requirements are appropriately...

  • Environmental Health Safety Specialist

    Found in: Appcast Linkedin GBL C2 - 2 weeks ago


    Cambridge, United States Randstad Life Sciences US Full time

    Immediate opportunity for an Environmental Health & Safety Specialist II to work with multi-national pharmaceutical company dedicated to pharmaceutical research and vaccine development. The HSE Associate Level Service Provider serves an important and highly visible role helping to ensure that site HSE Management System (HSE-MS) requirements are appropriately...


  • Cambridge, United States Randstad Life Sciences US Full time

    Immediate opportunity for an Environmental Health & Safety Specialist II to work with multi-national pharmaceutical company dedicated to pharmaceutical research and vaccine development. The HSE Associate Level Service Provider serves an important and highly visible role helping to ensure that site HSE Management System (HSE-MS) requirements are appropriately...

  • Associate Medical Director, Drug Safety

    Found in: Resume Library US A2 - 6 days ago


    Cambridge, Massachusetts, United States Biogen Full time

    Job Description What you’ll do: The Associate Medical Director, Global Safety Physician will be responsible for global pharmacovigilance for investigational and/or marketed products, including review and analysis of safety data, design of clinical trials, identification and investigation of safety signals, management of benefit-risk profile for assigned...


  • Cambridge, United States Relay Therapeutics Full time

    As a Senior Medical Director at Relay Tx, you will help advance our clinical pipeline from IND to proof of concept to registration. Specifically, you will collaborate with senior medical staff to drive clinical strategy, clinical trial design, and execution. Working cross-functionally with clinical project management, regulatory affairs, clinical operations,...


  • Cambridge, United States Relay Therapeutics Full time

    As a Senior Medical Director at Relay Tx, you will help advance our clinical pipeline from IND to proof of concept to registration. Specifically, you will collaborate with senior medical staff to drive clinical strategy, clinical trial design, and execution. Working cross-functionally with clinical project management, regulatory affairs, clinical operations,...


  • Cambridge, United States The Fountain Group Full time

    Onsite role in Cambridge, MAW2 Candidates only Manager Updates/Required Skills Must have Safety related experience within Research and Development or Pharma Employers Bachelor's degree Min of 3+ years of experience - direct safety-related experience Senior HSE level experience required Self-driven, ability to take on projectsPreferred / Nice to Have Skills:...

  • Safety Specialist

    Found in: beBee jobs US - 2 weeks ago


    Cambridge, Massachusetts, United States QData Full time

    Roles & Responsibilities Monitor manage and ensure delivery of projects in a deadline-driven environment. Author Technical SDLC deliverables Technical assistance for testing preparation and implementation of enhancements Contribute to the creation of operational support documentation Drive technical delivery and accountability of internal staff as well as...


  • Cambridge, United States ARTBIO Full time

    Job DescriptionJob DescriptionSalary: SummaryWe're seeking a Senior Scientist in Radiochemistry who will be responsible for technically designing, managing, and executing a radiopharmaceutical development and manufacturing plan for Pb212-drug candidates. The successful candidate will support radiolabelling. metal complexation, and formulation for our new...