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Medical Director CONTRACT

BioCryst Pharmaceuticals
United States, North Carolina, Durham
4505 Emperor Boulevard (Show on map)
Jan 16, 2025
Description

JOB SUMMARY:

The Medical Director, Global Drug Safety will implement and coordinate safety surveillance procedures for BioCryst products. Responsibilities include formulating safety surveillance policies and procedures if necessary; monitoring the safety profile of delegated products; interpreting the medical significance of incoming safety information; preparing assigned regulatory and ad hoc safety reports; serving as the BioCryst safety lead to Clinical Development Teams and business partners on assigned projects; and overseeing the activities of other Drug Safety personnel. The Medical Director, Global Drug Safety is also responsible for leading departmental initiatives for the development of pharmacovigilance best practices, acting as senior safety representative in company initiatives and mentoring junior drug safety colleagues.

ESSENTIAL DUTIES & RESPONSIBILITIES:



  • Develop & Lead safety activities and benefit-risk strategies for post-marketed products.
  • Oversee, Prepare, Contribute, and/or Review aggregate safety review documents (e.g., DSUR, PBRER), PSMF and selected clinical documents including regulatory filings and risk management plans.
  • Lead evaluation & management of signals emerging from any data source. Develop strategy for signal evaluation. Prepare and Review reports on safety signals (i.e., Safety Topic Reviews/ Signal Reports) and ad hoc regulatory responses.
  • Responsible for the medical review of all sources of safety information including ICSRs, product complaints, and requested medical information queries.
  • Contribute to safety labeling activities for BioCryst products and ensure safety labeling adequately reflects emerging post marketing safety profile.
  • Support the EU QPPV or other regional or local Qualified Person for PV relative to issues relating to assigned products.
  • Provide support to clinical development teams regarding emerging benefit-risk profile, appropriate safety monitoring during clinical trials and safety strategy for drugs in development.
  • Lead medical safety oversight of and execution of risk management strategies and RMP elements for assigned products.
  • Act as BioCryst safety lead on assigned projects with Business Partners, Vendors, Clinical Development Teams and Post Marketing Project Teams and in interactions with Medical Monitors and other BioCryst personnel.
  • Participate in company initiatives as senior drug safety representative.
  • May oversee activities delegated to other personnel.
  • Mentor junior drug safety personnel, including drug safety scientists.
  • Maintain current knowledge and understanding of regulations, ICH guidelines and industry practices in relation to pharmacovigilance.
  • Attend product team meetings, safety team meetings, company safety governance meetings, and regulatory interactions. Some travel may be required for safety meetings with partners, vendors, and regulatory authorities, and for attendance at conferences.
  • Other duties as assigned.



EXPERIENCE & QUALIFICATIONS:



  • MD or equivalent, with at least 3 years of Drug Safety experience required
  • Knowledge of GVP, ICH-GCP, and regional regulatory PV requirements
  • Vendor management experience a plus
  • Management experience a plus
  • Critical thinker and strong interpersonal skills
  • Excellent writing and oral communication skills in English
  • Ability to work with others at all levels and from a wide range of backgrounds in the company (incl. internal and external), able to lead through influence



The statements in this position description are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. The manager may assign additional responsibilities and assignments from time to time.

BioCryst is an equal opportunity employer and is committed to providing equal employment opportunities without regard to age, race, religion, sex, sexual orientation, gender identity, national origin, Veterans status, disability and/or other protected class characteristics. Additionally, BioCryst is committed to achieving its business objectives in compliance with all federal, state and local law.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c)
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