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PharmD Program Associate - Regulatory Strategy (Biotech)
98 100 - 160 100$
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Описание вакансии
Текст:
TL;DR
PharmD Program Associate - Regulatory Strategy (Biotech): Supporting global regulatory planning and execution for pharmaceutical products across clinical development, approval, and lifecycle management with an accent on regulatory pathways, submissions, safety data, and cross-functional delivery. Focus on drafting regulatory documents, analyzing clinical and safety data, managing vendors and timelines, and preparing strategies for interactions with global health authorities.
Location: Onsite in Tarrytown, New York, United States. Travel of up to 15% may be required. Applicants must be eligible to work permanently in the United States.
Salary: $98,100–$160,100 annually.
Company
Biotechnology organization developing pharmaceutical products through global clinical development, regulatory, and safety programs.
What you will do
- Support global regulatory planning and execution for clinical development, product approvals, and lifecycle management.
- Develop regulatory strategies and define pathways in collaboration with cross-functional partners.
- Draft documents for clinical sites and regulatory submissions.
- Analyze clinical-study and safety data for interactions with ethics committees, management, and regulatory authorities.
- Manage third-party vendors and maintain timelines for key results and deliverables.
- Participate in a 24-month rotational program with mentorship and optional exposure to another functional area.
Requirements
- PharmD graduate from an accredited ACPE College of Pharmacy, or a PhD in a related life-science discipline.
- PharmD and/or PhD degree must be completed by Summer 2027.
- Familiarity with evaluating clinical trials, scientific literature, and clinical data.
- Permanent U.S. work eligibility is required.
- Strong motivation to build a career in clinical sciences, global clinical operations, regulatory affairs, or safety sciences.
Nice to have
- Prior internship or rotational experience in the pharmaceutical or biotechnology industry.
Culture & Benefits
- Structured 24-month interdisciplinary development program with training from experienced mentors.
- Cross-functional assignments and hands-on experience across global development areas.
- Opportunities to travel to clinical sites and meetings with health authorities.
- Comprehensive rewards may include bonuses, equity, retirement benefits, health and wellness programs, insurance, paid time off, and family support benefits.
- Inclusive workplace with reasonable accommodations available during recruitment where required.
Hiring process
- Submit a resume and cover letter specifying the preferred program track; rank multiple tracks if applicable.
- Applications are accepted from August 24 through September 11, 2026.
- The interview process is described in the program brochure.
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