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Clinical Trial Manager

4 months ago

Newton, United States PSG Global Solutions Careers Full time

Apply now and our proprietary system will quickly have you in front of a live recruiter.
The Opportunity
Description
We're looking for a Clinical Trial Manager, working in Pharmaceuticals and Medical Products industry in Newton, Massachusetts, United States.

  • Supports the preparation and develops materials related to the training and presentations for Investigator Meetings.
  • Facilitates CRA project meetings.
  • Assists in the oversight of monitoring staff including tracking, reviewing and monitoring trip reports.
  • Escalates any trends with respect to data quality or study conduct to the appropriate CPM.

Our Client

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
  • Bachelors degree or nursing qualification is required (Scientific/health care field preferred)
  • 2+ years experience working in clinical research within a pharmaceutical company or CRO or similar organization
  • Strong attention to detail in composing and proofing materials, establishing priorities, scheduling and meeting deadlines
  • Ability to work in a fast paced environment with demonstrated ability to juggle multiple competing tasks and demands
  • Ability to work successfully within a cross-functional team
  • Strong knowledge of applicable computer and project management software packages
  • Excellent written and oral communication skills
  • Ability to interact with investigators, vendors, and internal colleagues
  • Knowledge of current regulatory requirements and guidelines governing clinical research
  • Ability to complete tasks to deadlines and resolve/elevate problems in a timely manner

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?