Clinical Project Manager-CPM (IVD)

Are you ready to put your in vitro diagnostic clinical trial leadership skills to work? Would you like to work with other industry leaders in an organization that partners with innovators in healthcare? Are you ready to work for a company that focuses on life-changing diagnostics? Read on if this describes you.

Beaufort seeks a skilled Clinical Project Manager to work alongside a top-notch team of clinical researchers. We participate in an exciting and growing industry and that growth fuels the need to continue to build our team. Our managers support the team while remaining, flexible and adaptable which continues to be a key to supporting our mission.

You might be wondering what a day in the life of a Clinical Project Manager at Beaufort looks like. This critical role can be counted on to:

Direct and coordinate the staff and activities to ensure goals and objectives are accomplished within projected timeframes and budget requirements
Review status reports and modify project schedules and/or plans as required
Prepare and present project reports for management, clients, or others
Act as the main point of contact/liaison between the Sponsor/Client and Beaufort
Conduct clinical protocol training and Standard Operating Procedure (SOP) training
Participate in business development activities such as assisting with the clinical aspects of RPFs and participating on scoping calls, as needed.
Act as the main point of contact for any study issues that arise and site escalation; may perform co-monitoring/monitoring visits as needed (e.g. Quality assurance, SWAT, interim monitoring visits, etc.)
Support team members to improve their efficiency and effectiveness at prioritizing work and improving performance

As you can see, there is a great amount of depth and breadth in this role. Because of this, we ask that you bring with you the education and/or experience that sets you up for success in this position. This generally looks like:

Bachelor's Degree required. (In science related field)
Minimum of three (3) years of project management experience
Minimum of two (2) years of experience in in-vitro diagnostic trials
Field monitoring and/or in-house Clinical Research Associate (CRA) experience required
Must have excellent analytical skills as well as the ability to communicate effectively with all levels of the company
Must be willing to travel to 25%. This includes travel to Beaufort offices in Virginia Beach, VA for trainings, meetings, etc.
Five or more years of professional experience monitoring multiple studies involving complex therapeutic areas simultaneously
CLS, MT (ASCP), CCRA, and or CCRP certifications preferred

While the above are just basic requirements, preferred qualifications include:

Prior experience as a project lead managing global in vitro diagnostics trials
A great collaborator with Senior Management
Documented experience with any of the applications listed

Beaufort provides a highly competitive compensation and benefits package. This position reports to the Senior Vice President, Global Clinical Operations.

Beaufort offers a different CRO experience. It’s not just about what we do, it’s how we do it. Together our team brings a level of passion knowledge and commitment to our projects and clients. We foster a culture of excellence specializing in in vitro diagnostic clinical project management and regulatory support.

At Beaufort you will be part of industry leading expertise with a shared sense of purpose and unwavering accountability to help clients achieve successful market authorization.

Beaufort is an equal opportunity employer and values diversity.

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Beaufort LLC

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Clinical Project Manager