Sr. Research Program Coordinator II - 117049

The Johns Hopkins University; Baltimore (MD); On-site; USD 48,000 - 85,000; Full time

Job summary

An established industry player is seeking an experienced Sr. Research Program Coordinator II to lead and coordinate complex clinical trials within a prestigious medical institution. This role involves managing daily operations, conducting participant visits, and ensuring compliance with regulatory standards. The ideal candidate will possess strong data management skills and a background in clinical research. Join a dedicated team focused on advancing surgical outcomes and enhancing patient care through innovative research. This opportunity offers a collaborative environment where your contributions will make a significant impact on clinical research and patient health.

Qualifications

• 5+ years of experience in coordinating clinical trials and managing data.
• Bachelor's degree required; Master's preferred.

Responsibilities

• Coordinate complex clinical trials and manage study participants.
• Prepare documents and reports for IRB and FDA compliance.
• Educate participants on study procedures and ensure adherence.

Skills

Clinical Trials Coordination

Data Management

Patient Interaction

Regulatory Compliance

Sample Collection

Education

Bachelor's Degree in related discipline

Master's Degree in related discipline

Job description

The Department of Surgery is currently searching for an experienced Sr. Research Program Coordinator II to implement and coordinate complex clinical trials in the Center for Surgical Trials and Outcomes Research (CSTOR). The Senior Research Program Coordinator II will provide for the daily operation, study visits, sample collection, data entry, and query resolution for multiple clinical research studies and trials; perform a variety of complex duties involved in the collection, compilation, documentation, and analysis of clinical research data.

Specific Duties & Responsibilities

• Collaborate with research team on scientific implementation, daily operation, and data management of interventional clinical trials.
• Manage participants on clinical studies while adhering to all protocol mandates.
• Conduct study participant visits, including inpatient wards and outpatient clinics.
• Provide for the acquisition and processing of clinical samples from study participants.
• Maintain study level documentation for assigned studies.
• Merge, create, and recode variables to prepare data for analyses.
• Prepare documents, annual reports, and amendments required by the IRB and FDA.
• Under the direction of surgeon principal investigators, determine patient study eligibility, obtain informed consent, and initiate patient randomization and enrollment.
• Act as a liaison for various studies with sponsors, study monitors, patients, and their primary care providers.
• Educate participants and families on protocol structure, study procedures, and study medication, ensuring understanding and adherence.
• Participate in staff meetings to report on screening, recruitment, and data collection progress and resolve problems.
• Work under the direction of the Principal Investigators and Director of Clinical Trials to ensure successful completion of clinical research projects.
• May be required to travel to satellite locations.

Minimum Qualifications

• Bachelor's Degree in related discipline. Related Master's preferred.
• Five years related experience.
• Additional education may substitute for required experience, to the extent permitted by the JHU equivalency formula.

Classified Title: Sr. Research Program Coordinator II
Role/Level/Range: ACRP/04/MC
Starting Salary Range: $48,000 - $84,100 Annually ($67,000 targeted; Commensurate with experience)
Employee group: Full Time
Schedule: M-F 8 -5
Exempt Status: Exempt
Location: School of Medicine Campus
Department name: SOM Sur Clinical Research Office
Personnel area: School of Medicine