Clinical Research Nurse Manager

New Haven
Oct 05, 2017
Nov 02, 2017
Employer Type
Direct Employer
Employment Type
Full Time
Our client is currently in need of a Clinical Research Nurse Manager who will serve as the central point of contact and be responsible for coordinating daily clinical research specific activities with Investigator Physicians and an interdisciplinary clinical trials support team. The incumbent will ensure protocol compliance, good clinical practice compliance, adherence to federal regulations, internal policies, and department SOPs by supervising the clinical research support staff in the conduct of clinical protocol activities. The Clinical Research Nurse routinely monitors research charts for accurate, complete, and timely data recording and is responsible for coaching and counseling direct reports as needed.
Manages and monitors policies, practices and procedures of licensed and unlicensed staff in their assigned translational working group
Ensure infrastructure to conduct clinical trials by evaluating the clinical, physical, technological, and staff resources required to ensure each clinical trial can be conducted in accordance with the study protocol, applicable policies and regulation while ensuring participant safety. Includes assigning nursing and research support staff to the disease team specific clinical trials.
Hires, trains, supervises and evaluates staff providing direction, training, support on a variety of research topics, including but not limited to: Informed Consent, enrolling study subjects, data management and monitoring/auditing of studies.
Collaborate with Therapeutic Working Group Leader (TWG) and Principal Investigator (PI) on assessment and implementation of highly complex trials for the research team. Includes identifying accrual targets, study activation timelines and metrics and resolving potential discrepancies and/or barriers to enrollment by prior to study activation.
Implements and manages internal practices of assigned translational working group that ensure compliance with University and federal requirements.
Manage oversight of protocol conduct and ensure that research site personnel and investigators, are conducting the study according to the protocols and Good Clinical Practice guidelines. Monitors federal and state regulations for new guidance, updates, or policies. Maintains a high degree of knowledge on these requirements to determine actions and follow directives that may be required to ensure University compliance with congruency review and reporting requirements.
Coordinates, oversees and participates in meetings including but not limited to Pre-study Visits, Site Initiation Visits, Monitoring visits, Multi-disciplinary Team meetings, staff meetings.
Liaison between the Grants and Contracts offices, investigators, and business managers to resolve congruency issues in a timely manner for projects within their assigned translational working group
Liaison between clinical and non-clinical related departments to resolve congruency issues in a timely manner for protocols/projects within their assigned translational working group.

BSN or ADN with a minimum of 4 years of experience in clinical trials research or the equivalent combination of education or experience.
Excellent clinical, organizational, and supervisory skills, with proven ability to successfully facilitate work across interdisciplinary teams to accomplish organizational goals.
Ability to comprehend and provide clear oral and written communication to safeguard the safety of clinical trial participants. Strong clinical and analytical skills. Proven ability to evaluate and assess subject's suitability for inclusion into studies, obtain informed consent, determine patient eligibility and coordinate patient enrollment.
• Strong knowledge of Good Clinical Practice guidelines. Proven experience interpreting federal, state, University and sponsor policies and regulations. Experience with interpreting complex oncology clinical trial protocols and federal, state, local guidelines.
Proven ability to manage several projects concurrently, while balancing competing priorities and deadlines. Extreme flexibility in work focus; ability to switch among several different projects without any adverse effects.
Demonstrated ability to report on the status of project deliverables and draft and submit project updates to Yale team and study sponsor.

Desired Experience:

Two years of experience in oncology research.
One year supervisory experience.
CT State Licensed Registered Nurse

Company Description:

At HumanEdge, we create great hiring experiences for candidates and clients alike. We do it by applying our skills, energy, integrity and understanding of both individual needs and market forces to make the right match for all types of positions, including traditional contract assignments, career-changing direct searches, and freelance gigs. We know that you're more than a skill set and cluster of job experiences -- you're a whole person with big dreams and ambitions. When you work with us, you partner with a firm committed to helping drive your success with ongoing support, guidance, and tangible opportunities. For over 30 years we've helped candidates like you make the right move in a wide array of industries and variety of positions

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