Sr. Research Program Coordinator II

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

Job summary

An established industry player in medical research is seeking a dedicated Sr. Research Program Coordinator II to lead the coordination of complex clinical trials. This pivotal role involves managing study participants, ensuring protocol adherence, and collaborating with a dynamic research team to drive successful outcomes. You will be responsible for data management, participant education, and liaising with various stakeholders. This is a fantastic opportunity to contribute to groundbreaking research in a supportive and innovative environment that values your expertise and dedication. If you are passionate about advancing clinical research and making a difference in patient care, we want to hear from you!

Qualifications

• 5+ years of experience in clinical research coordination.
• Bachelor's degree required; Master's preferred.

Responsibilities

• Coordinate and manage complex clinical trials and research studies.
• Ensure compliance with protocol mandates and data management.

Skills

Clinical Trials Coordination

Data Management

Informed Consent Process

Participant Education

Problem Solving

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