Current jobs related to Pharmacovigilance Scientist - Cambridge - Proclinical Staffing

  • Associate Director, Pharmacovigilance Scientist

    2 months ago

    Cambridge, United States Moderna, Inc. Full time

    The Role:Join Moderna Therapeutics enthusiastic and collaborative team and make a significant impact on the overall success of our novel messenger RNA approach to drug development. Reporting to the Senior Director of Pharmacovigilance, the PV Scientist will be a key contributor focusing on strategic input, support in clinical trial, perform signal management...

  • Senior Medical Director, Drug Safety and Pharmacovigilance

    4 months ago

    Cambridge, United States Intellia Therapeutics Full time

    Why Join Intellia?Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve more at Intellia. We have a single-minded determination to...

  • Senior Clinical Safety Scientist

    1 week ago

    Cambridge, Massachusetts, United States Apnimed Full time

    Job Title: Senior Clinical Safety ScientistApnimed is a clinical-stage pharmaceutical company dedicated to transforming the treatment of sleep apnea. We are seeking a highly skilled Senior Clinical Safety Scientist to join our team.Job Summary:The Senior Clinical Safety Scientist will play a critical role in the Clinical Development and Safety teams,...

  • Senior Clinical Safety Scientist

    4 weeks ago

    cambridge, United States Apnimed Full time

    Apnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...

  • Senior Clinical Safety Scientist

    4 weeks ago

    Cambridge, United States Apnimed Full time

    Apnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...

  • Senior Clinical Safety Scientist

    4 weeks ago

    Cambridge, United States Apnimed Full time

    Apnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...

  • Director, Safety Risk Management Scientist

    3 months ago

    Cambridge, United States Intellia Therapeutics Full time

    Why Join Intellia?Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve more at Intellia. We have a single-minded determination to...

  • Senior Clinical Safety Scientist

    5 days ago

    Cambridge, United States Apnimed Full time

    Apnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...

  • Senior Clinical Safety Scientist

    5 days ago

    Cambridge, United States Apnimed Full time

    Apnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...

  • Senior Clinical Safety Specialist

    2 weeks ago

    Cambridge, Massachusetts, United States Apnimed Full time

    {"title": "Senior Clinical Safety Scientist", "subtitles": ["Clinical Safety Lead", "Safety Data Analyst", "Pharmacovigilance Expert"], "description": "Job SummaryApnimed is seeking a highly skilled Senior Clinical Safety Scientist to join our Clinical Development and Safety teams. As a key member of our team, you will be responsible for performing core...

  • Senior Clinical Safety Specialist

    4 days ago

    Cambridge, Massachusetts, United States Apnimed Full time

    Senior Clinical Safety ScientistApnimed is a clinical-stage pharmaceutical company dedicated to transforming the treatment of sleep apnea. We are seeking a highly skilled Senior Clinical Safety Scientist to join our team.The ideal candidate will have a strong background in pharmaceutical development, with a focus on software-driven safety data analysis. They...

  • Senior Clinical Safety Specialist

    2 weeks ago

    Cambridge, Massachusetts, United States Apnimed Full time

    Senior Clinical Safety ScientistApnimed is a clinical-stage pharmaceutical company dedicated to transforming the treatment of sleep apnea. We are seeking a highly skilled Senior Clinical Safety Scientist to join our team.Key Responsibilities:Oversee safety and pharmacovigilance activities, ensuring data quality control and effective management of adverse...

  • Senior Director, Clinical Scientist

    7 days ago

    Cambridge, United States Moderna, Inc. Full time

    The Role:Moderna is seeking an experienced Clinical Sciences Team Leader to build and expand its clinical science capabilities. This role requires a strong track record of successfully building business capabilities in the biotech or pharmaceutical industry, advanced scientific and line function/team leadership skills, and a deep commitment to transforming...

  • Sr. Manager, Clinical Safety Scientist

    4 months ago

    Cambridge, United States Moderna, Inc. Full time

    The Role:Join Moderna Therapeutics enthusiastic and collaborative team and make a significant impact on the overall success novel messenger RNA approach to drug development. By joining our Clinical Safety Science Team, the Sr. Manager is responsible for performing core pharmacovigilance activities in partnership with the Global Medical Lead by supporting the...

Pharmacovigilance Scientist

3 months ago

Cambridge, United States Proclinical Staffing Full time

Pharmacovigilance Scientist - Contract - Fully remote role, Cambridge MA

Proclinical is seeking a dedicated Pharmacovigilance Scientist to join a Drug Safety team.

Primary Responsibilities:

This role will involve scenario planning, strategy analysis, portfolio prioritization, budget management and forecasting. The successful candidate will also be responsible for document management and authoring for aggregate safety reports. This is a fully remote position, offering the flexibility to work from anywhere.

Skills & Requirements:

  • Degree in a medical or healthcare related discipline (e.g., MSN RN, PharmD, Physician Assistant).
  • Experience in the pharmaceutical industry with a focus on drug safety/pharmacovigilance.
  • Familiarity with Document Management and use of VEEVA.
  • Strong skills in supporting the development and application of business process improvement methodologies.
  • Ability to manage teams and work in a matrix environment.
  • Knowledge of Argus Safety Databases and Signaling tools (e.g., Empirica).
  • Advanced knowledge of Global Pharmacovigilance regulatory requirements.
  • Strong planning, organization, written and oral communication skills.

The Pharmacovigilance Scientist's responsibilities will be:

  • Collaborate with the safety product lead and operational functions for document management and authoring of aggregate safety reports.
  • Prepare slides for the Safety Risk Management Team.
  • Work closely with the safety physician to analyze potential safety issues, including signal detection, evaluation, and management.
  • Contribute to signaling and data mining activities utilizing internal and external sources of data.
  • Assist in the evaluation of potential safety issues and quality risk assessment reports.

If you are having difficulty in applying or if you have any questions, please contact Bodin Forsen at Bo.forsen@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

INDSCIC