Clinical Engagement Lead job in Cambridge, USA

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Job type: Contract

Discipline: Project/Study Manager (CSM/CPM), Program Manager / Director, Clinical Scientist

Location: United States

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Clinical Engagement Lead - Contract - Onsite

Proclinical Staffing is seeking a Clinical Engagement Lead to join a cutting-edge biopharmaceutical company. This is a contract role located in Cambridge, MA.

Primary Responsibilities

The site Engagement Leader builds partnerships and commitment by active elicitation of information on site specific processes and feedback on trial design. During the trial, sustained engagement encourages bidirectional communication and facilitates learning networks for enhanced site performance. Moreover, site and community partnerships are leveraged to create locally designed dissemination plans for broader scientific reach and impact.

Skills & Requirements:

Scientific degree (Pharm.D.; Ph.D; MS…)
5-10 years experience in clinical research and clinical sites management in the pharmaceutical industry. Understanding of clinical trials and advanced knowledge of ICH-GCP, Clinical trials regulations, and applicable global and regional/country requirements.
Decision-making and autonomy: Able to make sound decisions after identification of an issue and being able to make careful consideration of various courses of action towards resolution.

The Clinical Engagement Lead will:

To ensure study remains on each site top priority list using an innovative site centered approach, establishing preferred connections with sites. Works very closely with the Medical team, to review steering committee charter, publication rules (favorizing sites competitions) always in the context in strengthening site engagement to the study.
Organizes regular Regional Group calls virtual & F2F (at sites, congress, IM)
Attendance including sites personnel, CRO and company (PMs, CMLs, MSLs) o Shares learning opportunity to troubleshoot challenges and streamline workflow. Encourage individual sites to lead discussion on area of expertise.
Target presentations and publications including site team representatives and advocacy partners present at advocacy and local community organization conferences. Identify appropriate dissemination outlets.
Disseminate lessons learned back to sites.
Gather site feedback to help tailor future trainings.
Individual sites call.
With either PI or study coordinator to share findings provided, findings provided back to sites through in-person meetings, monthly calls, and tip-sheets.
Give call- to actions to sites
Actively contributes to Monthly Newsletters
Study updates
Recognize site personnel.
Disseminate new research.
Feature new site and/ or personnel.
Highlight advocacy resources and events that site team can share with patients
Actively contributes to new sites identification/ feasibility (incl. identifying/reaching to community sites with less competition to have them participating in the study)
Actively contributes to recruitment boosting initiatives.
Identifies Vendors responsible for recruitment boosting and actively participate to vendor contract and start up in the study

Compensation:

$110 - $130 hourly

If you are having difficulty in applying or if you have any questions, please contact Bodin Forsen at (+1) 617-830-1769 or b.forsen@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

INDCR