GQR
Senior Safety Scientist/Safety Scientist
Location:
Remote or Hybrid (Waltham, MA) Our client, an innovative biotech company focused on autoimmune and rare diseases, is seeking a
Senior Safety Scientist/Safety Scientist
to join their growing Drug Safety & Pharmacovigilance team. In this role, you’ll play a critical part in ensuring the safety of clinical trial participants and maintaining compliance with global regulatory standards. Key Responsibilities Include: Monitoring safety data and identifying potential safety signals. Managing adverse event reporting, risk management, and safety documentation. Collaborating with cross-functional teams and PV vendors to ensure clinical trial safety. Supporting safety-related decision-making and contributing to regulatory submissions. Requirements: Master’s/PhD preferred Senior Safety Scientist: 7–10+ years of relevant industry experience. Safety Scientist: 5–7+ years of relevant industry experience. Expertise in global regulatory guidelines (FDA, EMA, ICH) and safety databases (e.g., Argus, Veeva). Why Join? Competitive salary and bonus potential. Stock options and a comprehensive benefits package. Opportunity to work in a fast-paced, growth-oriented biotech environment. This position offers a flexible work arrangement (remote or hybrid) and the chance to contribute to meaningful advancements in rare disease therapeutics. Seniority level
Mid-Senior level Employment type
Full-time Job function
Science Industries
Pharmaceutical Manufacturing and Biotechnology Research
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Remote or Hybrid (Waltham, MA) Our client, an innovative biotech company focused on autoimmune and rare diseases, is seeking a
Senior Safety Scientist/Safety Scientist
to join their growing Drug Safety & Pharmacovigilance team. In this role, you’ll play a critical part in ensuring the safety of clinical trial participants and maintaining compliance with global regulatory standards. Key Responsibilities Include: Monitoring safety data and identifying potential safety signals. Managing adverse event reporting, risk management, and safety documentation. Collaborating with cross-functional teams and PV vendors to ensure clinical trial safety. Supporting safety-related decision-making and contributing to regulatory submissions. Requirements: Master’s/PhD preferred Senior Safety Scientist: 7–10+ years of relevant industry experience. Safety Scientist: 5–7+ years of relevant industry experience. Expertise in global regulatory guidelines (FDA, EMA, ICH) and safety databases (e.g., Argus, Veeva). Why Join? Competitive salary and bonus potential. Stock options and a comprehensive benefits package. Opportunity to work in a fast-paced, growth-oriented biotech environment. This position offers a flexible work arrangement (remote or hybrid) and the chance to contribute to meaningful advancements in rare disease therapeutics. Seniority level
Mid-Senior level Employment type
Full-time Job function
Science Industries
Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr