Research Project Manager

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Our client, a leading non-profit healthcare system, is looking to hire a Research PM to assist the clinical research team.

The Research Project Manager will play a pivotal role in the development and execution of comprehensive workflows and project tracking processes, ensuring compliance in clinical trials across diverse research programs or divisions. This role will collaborate with interdisciplinary teams, fostering process improvement and emphasizing training clarity while maintaining high ethical standards.

This Role Offers:

• Competitive wage supplemented by a comprehensive benefits package – medical/dental/vision, 401(k) match, etc.
• A supportive environment recognized for its commitment to industry excellence.
• Access to advanced learning programs aimed at fostering personal and professional development.
• A culture that promotes high performance, exceptional care, and positive outcomes.

Focus:

• Effectively oversee all elements of research trials within the designated program or division.
• Formulate and establish workflows, protocols, and recommendations for staff and patients, ensuring adherence to quality and compliance standards.
• Preserve precise documentation, monitoring, and reporting of clinical trial data through collaborative efforts with fellow research team members.
• Coordinate, monitor, and report on both internal and external research meetings, fostering seamless communication.
• Supervise protocol feasibilities, site selection, and the initiation of studies to expedite the process.
• Dedicate attention to the continuous enhancement of processes within the research program.
• Act as a vital link between investigators, funding entities, and external contractors, facilitating smooth communication.
• Evaluate study performance, pinpoint potential challenges, and escalate issues to higher management when required.
• Provide support in the administrative aspects of clinical trial conduct and ensure compliance efforts are upheld.

Skill Set:

• Bachelor’s degree in a scientific or medical field. SOCRA and/or PMP certifications, a plus.
• 3+ years of clinical healthcare experience with a focus on project management and oncology research.
• Proficiency in clinical office management and workflow.
• Strong knowledge of GCP guidelines and other related regulations.
• Possesses a solid grasp of Good Clinical Practice (GCP) guidelines and relevant regulatory frameworks.
• Excels in cross-functional collaboration, exhibiting outstanding time-management skills.
• Displays strong analytical abilities and a high level of proficiency in Microsoft applications, including Excel, Word, Outlook, and others.
• Communicates effectively with a keen awareness of deadlines and time-sensitive tasks.
• Brings experience with Access, database tools, EndNote, and Adobe Acrobat, which are valuable assets.

About Blue Signal:

Blue Signal is a leading executive search firm specializing in healthcare recruiting. Our healthcare recruiters have expertise in placing high-performing talent in healthcare IT, medical devices, biotechnology, pharmaceuticals, etc. Learn more at bit.ly/3G5DbWr