Site Feasibility Liaison II

Key Accountabilities:

Review draft site lists, communicate with sites to ensure high response rates, co-ordinate CDA collection – if necessary, query inconsistent/incomplete survey information, provide data-driven recommendations with regards to site selection

Conduct phone interviews with Investigators or site personnel to discuss standard of care, trends, patient barriers, protocol design considerations

Support the central feasibility teams with local insight to support country strategy, protocol development and new business awards.  Provide accurate, timely and realistic information.

Proactively work to understand healthcare re-imbursement, trial infrastructure, patient motivations, patient support groups, site networks, new potential sites/Investigators for consideration in your country, region, therapy area

Understand, communicate, and help to mitigate the risks to delivery for your country, region, therapy area.

Provide input on sites’ previous trial performance in similar indications, highlight fast starter sites that can be initiated within up to 3 months

Proactively work to ensure accuracy of critical information held in the Investigator Intelligence Platform relevant to your country, region or therapy area.  Work to build out valuable profile information for key sites to improve efficiency and improve the site experience.

Update the TMF system for recommended sites to support timely CRA resource assignment.

Actively work with clinical and medical experts in your country to promote collaboration and to facilitate information gathering.

Work closely with central feasibility counterparts to ensure a common understanding of risk and to promote the consideration of your country or region in future trials.

Develop and maintain collaborative relationships with Investigators and site personnel

Encourage and promote a culture of innovation and respect with the patient first and foremost.

Skills:Autonomous, driven, takes pride in quality of workIndependent thinkerExceptional analytical and problem-solving skillsEffective interpersonal, presentation, oral and written communication skillsCapability to work in a matrix environment and to value the importance of teamwork.Ability to manage multiple tasks, to be flexible and to prioritizeSense of urgency to respond to client requestsStrong computer skills

Knowledge and Experience:Several years Pharmaceutical/CRO Industry Experience in Clinical ResearchMultiple years in clinical management/feasibility management of global clinical trials with significant local clinical experienceDemonstratable understanding and experience in selecting and starting up clinical trial sites

Education:Degree / further degree. MSc, MBA, Ph.D. or equivalent preferredScientific/Medical/Nursing background

Language Skills

•      Fluent in English, oral and written

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