RN, Clinical Trial Manager
About The Position
Opportunities with Reliant Medical Group, part of the Optum family of businesses. Join a community-based, multi-specialty, physician-led organization where you will work with talented peers on a common purpose: improving the quality, cost and experience of health care. Here, we focus on delivering the best patient care, rather than volume. Through innovation and superior care management, we support patients and your well-being as a team member. Join a team at the forefront of value-based care and discover the meaning behind Caring. Connecting. Growing together. This position is responsible for the overall management of individual research projects from pre-study inquiries to post-study follow-up and related duties.
Requirements
- Graduate of an accredited School of Nursing
- Currently licensed as a RN in the State of Massachusetts
- 3+ years of relevant experience
Nice To Haves
- Proven excellent interpersonal, communication and organizational skills
- Proven excellent time management and problem-solving skills, as well as solid attention to detail
- Ability to adapt to changing priorities and to manage challenges and conflicts within multiple assignments
Responsibilities
- Management of clinical trials.
- Manages, supervises, and trains other research nurses, research assistants, and other support staff.
- Explains protocol criteria in terms easily understood
- Acts as the key liaison with physician investigator or others
- Manages required study activities with other departments.
- Identifies and resolves issues as required
- Assesses organizational processes, including Standard Operating Procedures (SOP), and identifies ways to improve procedures.
- Creates and maintains departmental SOPs as appropriate
- Meets with sponsor representatives to evaluate study feasibility and site appropriateness
- Attends research protocol development or evaluation meetings as required by the sponsor or principal investigator
- Ensures inquiries from patients, sponsors, physicians, and staff are appropriately routed
- Executes IRB approved research protocols.
- Performs study-related procedures including, but not limited to, patient recruitment, informed consent, physical assessment, medical history, vital signs, administration of study medication, preparation and handling of laboratory specimens, identification of adverse events, and collection of all required data
- Assesses performance of ongoing clinical trials and develops action plan to address performance gaps
- Attends a variety of meetings with sponsor, investigator, or regarding patient needs.
- May conduct home visits to treat patients
- Interfaces with pharmaceutical monitors, FDA and other regulatory agencies.
- Documents to meet federal standards
- Act as liaison between sponsor, investigator, patient, IRB, SVH, and other clinical departments
- Notifies research director or others of unexpected circumstances that affect study performance and/or budget
- Resolves billing issues (sponsor payments, patient billing issues, reimbursement issues)
Benefits
- a comprehensive benefits package
- incentive and recognition programs
- equity stock purchase
- 401k contribution
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
