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Project Management (Clinical Research)
Ref No.: 16-03051
Location: Blue Bell, Pennsylvania
Job Description:
The Senior Project Manager (Clinical Research) will serve as the primary contact with the sponsor for all study related items, with oversight of all aspects of trial conduct, from study start-up through close-out in accordance with company and project specific SOPs, guidelines, budgets, timelines and contracts.

Primary responsibilities:
  • Oversee all aspects of trial conduct from Study start-up through close-out
  • Manage project per the scope of work and within the contracted budget
  • Ensure project is conducted according to UBC and client SOPs
  • Develop plans to achieve contracted milestones (i.e. project plan, clinical management plan, monitoring plan, training plan, communication plan); monitor project progress against the established plans and ensure compliance with plans
  • Prepare project timelines and prepare or coordinate project development of deliverables
  • Ensure project budget is tracked against contract milestones
  • Serve as UBC primary contact with sponsor
  • Lead internal project and client conferences
  • Focal point for resolving project team member questions
  • Supervise assigned staff including clinical research associates (CRAs) and clinical trial specialists (CTS),
  • Other duties as assigned by management

Requirements:
  • BA/BS degree required
  • Minimum of 3 years of direct project management experience at a CRO or 5 or more years of clinical trial experience
  • Excellent supervisory, interpersonal and presentation skills
  • Must possess knowledge of regulatory requirements for trial conducts (i.e. Good Clinical Practice, ICH guidelines, etc.)
  • 10% travel required

More Information:
  • Travel: Yes, 10 % of the Time
  • This position is: New Position
  • Is there a bonus structure? 15%
  • Is there equity? Yes
  • Who does this position report to?
  • This person can be located in Blue Bell, PA and work from our office there Current work schedule is 3 days from the office and 2 from home
  • Does this position have direct reports? No
  • What are the 3-4 non-negotiable requirements on this position?
  • Min 3 years of direct project management experience at a CRO or 5 or more years of clinical trial experience.
  • This position is NOT a 100% work from home role. The candidate must be open to working from the office 3 days a week.
  • Must have knowledge of regulatory req. for trial conducts.
  • What are the nice-to-have skills?
Cardiovascular background Level III and IV trial experience Plus if individual has more than 3yrs at a CRO
What is exciting about this opportunity?
  • Multi therapeutic areas We continue to grow This role positions individuals for possible movement upwards within the company as they will have high visibility from leadership