Clinical Research Coordinator - Remote Trials & Recruitment

University of Pennsylvania; Woodworth (OH); On-site; USD 48,000 - 59,000; Full time

Benefits offered by this job

Health benefits

Tuition benefits

Retirement plans

Time off

Long-term care insurance

Wellness program

Professional development

University resources

Discounts

Flexible hours

Home ownership help

Adoption assistance

Job summary

The University of Pennsylvania’s Perelman School of Medicine in Philadelphia is seeking a Clinical Research Coordinator B to assist in managing Polyendocrine Metabolic Ovarian Syndrome studies. You will screen and recruit participants, enroll subjects, and collect clinical data at study visits, working closely with the Principal Investigator and the study team.

You may help with IRB filings, prepare manuscripts and grant proposals, and coordinate regulatory activities.

Qualifications

• Bachelor’s Degree with 2-4 years related experience in research and clinical study methodologies or equivalent combination of education and experience is required.

Responsibilities

• Study recruitment: Interview and evaluate participants for enrollment, obtain informed consent, conduct enrollment visits remotely and in person.
• Study visit scheduling and follow-up: Plan and assess overall study management, intercept and respond to participant calls, conduct follow-up per protocol.
• Review and prepare protocols for original, pharmaceutical, and government-sponsored clinical trials.
• Prepare protocols, informed consent documents, data collection forms and advertising for regulatory approval.
• Organize site visits from sponsors and regulators; attend investigator meetings as needed.

Education

Bachelor’s Degree with 2-4 years related experience in research and clinical study methodologies or equivalent

Job description

The University of Pennsylvania’s Perelman School of Medicine in Philadelphia is seeking a Clinical Research Coordinator B to assist in managing Polyendocrine Metabolic Ovarian Syndrome studies. You will screen and recruit participants, enroll subjects, and collect clinical data at study visits, working closely with the Principal Investigator and the study team.

You may help with IRB filings, prepare manuscripts and grant proposals, and coordinate regulatory activities.