Existing employer? Sign in
New York Medical College
Nurse Research Project Manager
IRB
Edtech.com's Summary
New York Medical College is hiring a Nurse Research Project Manager to coordinate and administer clinical research projects within the department of medicine. The role involves managing study visits, ensuring regulatory compliance, handling documentation, and delivering nursing care to research participants from study start-up through completion under the guidance of the principal investigator and research leadership.
Highlights
- Coordinates clinical studies from initiation to close-out under PI direction.
- Organizes study start-up tasks including feasibility assessments, regulatory submissions, and scheduling.
- Prepares and maintains study documentation such as source notes, case report forms, and regulatory binders.
- Conducts participant visits and ensures accurate data capture while monitoring participant safety and adverse event reporting.
- Performs clinical nursing tasks including biospecimen collection and study-drug administration according to protocols.
- Facilitates communication among investigators, clinical staff, sponsors, and ancillary departments like pharmacy and labs.
- Requires Bachelor of Science in Nursing, RN license with DORA, BLS certification, and 1-2 years of clinical research experience plus 2+ years bedside nursing. Critical care experience preferred.
- Must be proficient with Microsoft Office Suite and knowledgeable about IRB submission platforms and regulatory databases.
- Familiarity with OMB Uniform Guidance and NIH grant policies is necessary.
- Salary range: USD $109,200 to $136,500 per year.
Nurse Research Project Manager Full Description
Overview:
The Nurse Research Project Manager plays a key role in the administration and coordination of clinical research projects, supports the day-to-day conduct of clinical research and other sponsored projects while performing nursing responsibilities in accordance with protocol requirements. This position provides direct coordination of study visits, ensures regulatory and protocol compliance, manages study documentation, and delivers patient-centered clinical care to research participants. This position plays a key operational role within the department of medicine, assisting with studies from start-up through completion under the guidance of the PI and research leadership.
Responsibilities:
Responsibilities:
- Coordinates assigned clinical studies from initiation through close-out under PI direction
- Organizes study start-up activities, including feasibility, regulatory submissions, and staff scheduling.
- Prepares, maintains, and reconciles study documentation such as source notes, case report forms, and regulatory binders.
- Schedules and conducts participant visits; ensures accurate data capture and protocol adherence.
- Monitors participant safety, performs follow-up, and reports adverse events promptly.
- Serves as a liaison between investigators, clinical staff, sponsors, and ancillary departments (pharmacy, lab, imaging).
- Assists in IRB submissions, amendments, and continuing reviews.
- Maintains participant confidentiality and secure handling of study records.
- Serves as a liaison between investigators, clinical staff, sponsors, and ancillary departments (pharmacy, lab, imaging).
- Performs clinical duties per protocol, including biospecimen collection, study-drug administration, EKGs, and other nursing procedures within scope of practice.
- Provides patient education and informed-consent discussions in coordination with the PI.
- Collaborates with care teams to integrate study participation with standard clinical treatment.
- Advocates for participant safety and wellbeing throughout the research process.
Qualifications:
Education/Experience:
- Bachelor of Science in Nursing, required
- Licenses or certifications:
- RN-Registered Nurse - DORA - Department of Regulatory Agencies required.
- BLS-Basic Life Support (BLS/CPR) - AHA - American Heart Association or American Red Cross required.
- CITI training
- Prior experience:
- 1-2 years of clinical research
- 2 (+) years of Clinical Bedside Nursing
- Critical Care Experience Preferred
Knowledge/Skills/Abilities
- Ability to manage project timelines and competing priorities
- Familiarity with OMB Uniform Guidance and NIH grant policies
- Strong communication and documentation skills
- Detail-oriented and capable of navigating complex institutional processes
- Proficiency in Microsoft Office Suite
- Knowledge of IRB submission platforms and regulatory databases
Physical demands:
- Frequent sitting for administrative work
- Occasional walking and standing in clinical areas
- Occasional lifting of study materials and files (under 20 lbs)
Environmental demands:
- In Person office and clinical exposure
- Potential exposure to patient care settings and biological samples
Minimum Salary: USD $109,200.00/Yr. Maximum Salary: USD $136,500.00/Yr.
Similar Jobs
Project Manager, Strategic Operations, College of Engineering
Pennsylvania State University
🇺🇸 University Park, Pennsylvania
Project Manager IV for Information Services
Liberty University
🇺🇸 Remote - US
Project Manager IV, Transformation
Western Governors University
🇺🇸 Salt Lake City, Utah
Staff Technical Program Manager
Duolingo
🇺🇸 New York, New York
Program Manager, Experience
DeVry University
🇺🇸 Remote - US
