Sr. PV Scientist (Cambridge)

Compensation

: $94,360.00 - $141,170.00 /year *

Employment Type

: Full-Time

Industry

: Scientific Research



Job Description

We are searching for a PV Scientist consultant that is a creative, resourceful and integrative thinker. The person in this role works closely with the Global Safety Lead (GSL) and with the VP of Drug Safety and Pharmacovigilance and provides pharmacovigilance and signal detection expertise. Effective communication skills will be key as this role provides an excellent opportunity for close collaboration with colleagues from other functions such as Clinical Development, Clinical Operations, Regulatory Affairs and Medical Affairs.The PV Scientist consultant will provide scientific/clinical expertise, strategic input, and support for deliverables and activities associated with signal management activities, safety and benefit-risk evaluations for assigned products, management of potential safety issues for assigned products, evaluation of databases for safety signals, and drafting of responses to regulatory inquiries on product safety issues including oversight of aggregate reporting for assigned product.

Roles and Responsibilities

  • Overseeing aggregate reporting, clinical trial activities, signal management, literature review, and ad hoc regulatory responses for assigned product group
  • Lead product safety surveillance activities for assigned product(s)during all phases of the product life-cycle
  • Review study protocols, statistical analysis plans and other clinical study-related documents
  • Review standard design of tables, figures, and listings for safety data from clinical studies
  • Manage updates to Investigator Brochure, Company Core Safety Information and other Reference Safety Information
  • Signal detection, evaluation, and management
  • Implement signal detection strategy approved by GSL and VP of Drug Safety and Pharmacovigilance
  • Review adverse event data, literature, and other safety-relevant data for the purpose of signal detection
  • Prepare review of potential safety signals for GSO and VP of PVRM
  • Provide safety contents for risk management plans
  • Assisting in the successful implementation, execution and maintenance of safety processes and systems that conform to the companys business strategy, industry standards and compliance with global regulations
  • Qualifications

    Basic Qualifications:

    o Advanced degree (RN, PharmD, NP, PhD, MD, MPH, NP, or DVM with specialty board certification)

    o Minimum of 6 years pharmacovigilance experience, including experience in aggregate safety reports and safety signal management

    Preferred Qualifications:

  • Expertise in the following; Argus Safety Database, MedDRA, Sharepoint, Microsoft Office, Excel
  • Sound clinical acumen and decision making
  • A proactive and innovative approach and a flexible, hands-on nature that works with a high sense of urgency.
  • Ability to review, synthesize and analyze and communicate (verbally and in writing) complex safety data and clinical/pharmaceutical information
  • Expertise in international regulations governing drug safety (US and EU) for pre and post-marketing
  • Demonstrated leadership and collaborative skills necessary to influence across functions and earn credibility across a complex and rapidly growing organization.
  • Level will be commensurate upon experience and qualifications.
  • Excellent oral and written communication skills
  • Prior experience contributing to the development (process improvement, training, etc.) of a drug safety would be desirable

  • Associated topics: biopharma, diet, dietician, histology, immunology, medicine, microbiological, nutrition, pharmacy, virus * The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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