Regional Site Liaison - Clinical Operations

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BlueRock Therapeutics

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Stem Cell Therapeutics • Engineered Cell Therapy • Cardiology • Neurology • Immunology

201 - 500

💰 $225M Series A on 2016-12

Description

• The Cambridge, MA location is seeking a highly motivated person who possess proven clinical site engagement experience in early and late phase clinical trials, to join the Clinical Operations team as a Regional Site Liaison (RSL), reporting to the Senior Director, Site and Patient Engagement. • The RSL will support study teams and the broader Development organization by providing local relational and operational support to investigative site personnel, with the goal of building long-term relationships between the sites and BlueRock Therapeutics. Site territory will be US. • The RSL is responsible for providing local relational and clinical operations support to investigative site personnel and CRAs to strengthen customer relations, ensure customer satisfaction and support BRT clinical trials at the site. • In this role, the RSL will serve as the primary BRT resource for sites conducting BRT clinical trials. The RSL will also be integral in helping build out globally a BRT reputation as leaders in cell+gene therapy.

Requirements

• The primary goal of this position will be to build relationships with site personnel, including being responsive to their requests for information, problem solving and/or issue resolution. • Minimum of a Bachelors’ degree (BS preferred) in a scientific field of study with a minimum of 4 years of relevant experience working in the clinical trial setting (i.e., either at a clinical site or in the pharmaceutical/ biotech industry) required. • Experience/knowledge in Neurology, Ophthalmology, Immunology preferred, with the ability to learn future therapeutic areas/disease states. • Ability to build and maintain strong relationships and credibility with investigative site personnel. • Exceptional customer service skills with excellent leadership, interpersonal and communication skills and deep understanding/appreciation of the working relationships between investigative sites, CRA/CRO and the Sponsor. • Have experience with site operations and be knowledgeable about the conduct and monitoring of clinical studies. • Have an awareness of local country requirements including necessary institutional/health authority approvals (e.g., IRBs, FDA, EMEA, etc.). • Possess strong organizational skills with an ability to align priorities, lead multiple tasks/activities and manage time independently.