We're looking for a Contract R&D Project Planner II, working in the Pharmaceuticals & Medical Products industry in Madison, New Jersey, United States.
Develops and maintain high quality, realistic, cross functional clinical trial plans from protocol concept through completed clinical study reports.
Identifies gaps and risks in the study plans and work with the team and Management to proactively develop solutions which will increase efficiency and minimize timelines.
Presents clear clinical study plan reports to stakeholders.
Operates within the Growth Product Flow (GPF) Governance Board model for Project communication and accountability.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years’ experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Life science and/or business degree with at least 3 years of experience in the industry, preferably with a sponsor or CRO. MS degree and PMP certification desirable.
1-3 years of Project Management experience required.
Knowledge of and experience with clinical study/trial operations processes.
The pay range we're offering is 65 - 73 per hour. This position may present an opportunity to go permanent.
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.