Principal Scientist

Globalchannelmanagementinc

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Marlborough, MA, us on site Until 8/22/2026 First posted March 23, 2025 Last posted March 23, 2025
Job description

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation.  Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function.  Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. 


Principal Scientist needs Minimum of 4-6 years in a pharmaceutical
organization or related industry with a minimum of 2-3 years
pharmaceutical experience in a clinical safety or regulatory affairs


Principal Scientist requires:


Master Degree or PhD in Medical Science, Pharmacy or Nursing preferred.

  • Minimum
    of 2-3 years of medical writing experience (Prefer experience in
    writing pharmaceutical reports such as PSURs, Clinical Study Reports,
    safety sections of the ISS and/or Common Technical Document, or white
    paper) and/or experience in Medical Surveillance and Risk Management.
  • Proven understanding of clinical disease state and implications of treatment.
  • At ease with data and statistics.
  • Knowledge
    of ICH, US & EU regulations and requirements for pharmacovigilance
    (experience with world-wide safety reporting regulations and guidelines)
    and Risk Management.

Required

  • CLINICAL SAFETY
  • CLINICAL STUDY
  • CLINICAL TRIAL
  • PHARMACOVIGILANCE
  • CLINICAL TRIALS


Principal Scientist duties:


  • Work with others to determine topics for discussion in Section 9; prepare first draft of Section 9 for Medical Director review
  • Follow-up on issues identified in regulatory responses (e.g., assessment reports)

$95/hr

12 MONTHS

About this role

Summary

Conduct clinical safety and pharmacovigilance activities, prepare regulatory documents, and support clinical trial reporting.

Job title

Principal Scientist

Experience level

4-6 years in industry, 2-3 years in pharmaceutical

Industry

pharmaceutical

Location requirements

Marlborough, MA, US; remote not specified

Salary

$95/hr

Management role

No

Skills & keywords

Required skills

clinical safetyclinical studyclinical trialpharmacovigilance

Preferred skills

medical writingrisk managementregulatory knowledgedata analysis

Specializations

clinical safetyclinical studyclinical trialpharmacovigilanceregulatory affairs
Locations

Structured locations inferred from the posting.

Marlborough, MA, USA

On-site City