Manager of Research Programs

Research Program Manager

When you join the growing BILH team, you're not just taking a job, you're making a difference in people's lives.

Under general direction, the Research Program Manager will be responsible for managing, promoting, cultivating and overseeing all aspects of research, including management of a clinical research department(s).

Essential Duties & Responsibilities, Including But Not Limited To :

• Manages and oversees a clinical research program(s). Leads the department in all aspects of the daily research operation.
• Directly supervises the day-to-day operations of research providing direction and support to staff as needed.
• Oversees and ensures staff compliance with the research protocols of the department.
• Utilizes problem-solving skills and creates a proactive work environment in the maintenance of optimal department functioning.
• Evaluates and revises departmental research practices and procedures.
• Coordinates and facilitates research project team meetings, including creating agendas and generating minutes and action items.
• Possesses direct knowledge and experience in the implementation of all aspects of clinical trials research complying with research SOPs, GCP, FDA and OHRP regulations; ensures adherence to regulations and educates study team members.
• Functions as a resource and educator for research study team members and other colleagues related to research conducted within the department.
• Acquires detailed knowledge of studies so to serve as a specialist; Grasps the scope and objectives of projects.
• Triages calls from physicians, nurses, research staff or other colleagues.
• Educates investigators and ensures necessary and up-to-date trainings as applicable (e.g., CITI certifications).
• Evaluates and recommends recruitment efforts and practices.
• Monitors study enrollment; Identifies and addresses recruitment barriers.
• Manages conflict.
• Expands research opportunities by soliciting sponsors and CRO's for new trials : Actively seeks new research opportunities.
• Completes and submits trial feasibility forms; coordinates and obtains non-disclosure agreements.
• Reviews new protocols for feasibility, capability, logistics, personnel needs, etc.
• Establishes relationships with sponsors and / or CROs; arranges and / or conducts pre-study qualification and site visits.
• Develops new research initiatives in collaboration with physicians and sponsors; project management.
• Assists physicians with study protocol development; development and management of single center and / or multicenter projects as a sponsor-investigator.
• Assists in designing studies of drug utilization, clinical practices, and patient care processes.
• Assists with chart review submissions and implementation.
• Designs and implements improvement projects based on study results.
• Actively involved in development of research trial budgets; works closely with Research Finance to develop appropriate budget and contract preparation and negotiation; works collaboratively with Research Finance to oversee Medicare compliance in research visit billing; monitors research budget and corresponding enrollment status.
• Ensures research staff is operating within budget constraints.
• Assists with the acquisition, development, submission and maintenance of grants; seeks out funding opportunities.
• Assists in preparing summary reports, study results, poster presentations and manuscripts for publication; reviews scientific literature.
• Maintains an up-to-date listing of research activities, including research publications and presentations.
• Assists with statistical planning and analysis as applicable, functions as a liaison between statisticians and physicians.
• Participates in continuing education activities and attends conferences / seminars to maintain current knowledge of clinical study affairs and issues.
• Participates and assists in other research projects and initiatives as necessary.
• Is a team player within the department.
• Is flexible with time when applicable.

Organizational Requirements :

Minimum Qualifications :

Education :

Bachelor's degree required; Master's degree preferred.

Licensure, Certification & Registration :

CCRP / CCRC Certification or equivalent Certification preferred.

Experience :

7+ years of direct work-related experience in a research setting required. Leadership and project management experience required; Epic experience a plus.

Skills, Knowledge & Abilities :

As a health care organization, we have a responsibility to do everything in our power to care and protect our patients, our colleagues and our communities. Beth Israel Lahey Health requires that all staff be vaccinated against influenza (flu) as a condition of employment.

More than 35,000 people working together. Nurses, doctors, technicians, therapists, researchers, teachers and more, making a difference in patients' lives. Your skill and compassion can make us even stronger.

Equal Opportunity Employer / Veterans / Disabled