CRA Manager (remote-based)

$130000 - $140000 per annum
  1. Permanent
Massachusetts
  1. Clinical Operations, Clinical Trial Administration
Posted: 02/06/2021
BBBH16657

This vacancy has now expired. Please see similar roles below...

Hobson Prior are looking for a CRA Manager to join a world-wide Clinical Research Organisation who are dedicated to excellence in supporting the advancement of public health and biopharmaceutical origination. For more information on this exciting role please get in touch now!

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

  • Responsible to coordinate all monitoring aspects in the execution and support of clinical trial activities.
  • Supervises and ensures CRA team members are compliant with SOPs, sponsor and regulatory agency expectations for site monitoring activities.
  • Partakes on internal, site and sponsor teleconferences and meetings to address monitoring activities outlined in statements of work.
  • Critically reviews study protocols, study documents, monitoring reports and Sponsor required plans for communication, monitoring and other required plans.
  • Implements full scope and risk-based monitoring programs.
  • Develops and implements tracking systems for key monitoring activities and evaluates defined milestones for these activities.
  • Reviews and approves travel, expense report and timesheets.
  • Conducts co-monitoring activities (feasibility, qualification or selection, interim, close out visits, for cause and other visits) as required.
  • Partakes as a team leader in project planning, implementation, problem solving, tracking milestones and deliverables.
  • Communicates with the Sponsor and the study team.
  • Partakes in corporate initiatives as requested.
  • Any other assigned duties.

Requirements:

  • Requires a bachelor's degree and a background in clinical research, public health, biological sciences, or other related fields.
  • At least 5 years of monitoring experience in clinical trials.
  • Proven supervisory skills and excellent verbal and written communication skills.
  • Previous experience in any of the areas of ophthalmology, transplantation, neurology, vaccine and infectious diseases, cancer, maternal/child health and substance abuse preferred.
  • ACRP CCRA or equivalent certification preferred.
  • Ability to independently plan, lead and summarize conference calls or meetings with project staff, clinical staff, vendors and sponsor representatives.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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