Alnylam Pharmaceuticals-Clinical Science Postdoctoral Research Fellow

Northeastern University • Newton, MA

122d • $59,425 - $83,935

About The Position

Northeastern University Pharmaceutical Industry Fellowships Program is a two-year experiential program designed to advance lifelong learning and the education and training of Pharm.D. graduates. A key element of the program’s success is preparing Fellows to meet evolving workforce needs across various sectors of the pharmaceutical industry. Fellows have the opportunity to work closely with our innovative biopharmaceutical industry partners, while engaging with Northeastern University faculty in professional and career development, teaching, service, and scholarly activities. In partnership with Northeastern University, Alnylam Pharmaceuticals is offering a two-year Clinical Science fellowship, based in Cambridge, MA.

Requirements

• Doctor of Pharmacy degree from an ACPE-accredited institution.
• Eligible for pharmacist licensure in the State of Massachusetts.
• Excellent oral and written communication skills.
• Strong time management and leadership abilities.
• Ability to work independently and take initiative on a variety of projects at both the industry site and Northeastern.
• Proven project management experience.
• Ability to manage multiple priorities and work in a fast-paced, matrix environment.

Responsibilities

• Development of key documents including clinical development plans, protocol concepts and full protocols for product(s) in early development along with contributing to activities for product(s) in later stages of development, including NDA filings.
• Contribute to the development of clinical sections of regulatory documents such as Investigators’ Brochures, briefing books, safety updates, IND/NDA submission documents, and responses to Health Authorities questions.
• Engagement in medical data review and analysis during study execution to ensure integrity of accruing study data.
• Develop effective working relationship with key investigators in assigned programs to optimize scientific quality/innovation of clinical study design, execution, reporting and publication.
• Contribute to trial-related advisory boards.
• Participate in investigators meetings and protocol training meetings.
• Coordinate the real time availability of quality clinical trial data, including safety, efficacy, pharmacokinetic and biomarker data, to provide consolidated information for data review meetings.
• Create content to support internal and external clinical and scientific discussions on assigned programs and therapeutic areas.

Benefits

• Medical insurance
• Vision insurance
• Dental insurance
• Paid time off
• Tuition assistance
• Wellness & life benefits
• Retirement benefits
• Commuting & transportation benefits

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Ph.D. or professional degree