Clinical Studies Coordinator I, Cancer Biology, part-time

Part-time, 24 hours per week.

About the role

Under general supervision, responsible for the compilation and collection of data, recruitment of subjects, and general coordination of clinical studies. The coordinator will collect, process, store, and maintain research specimens and associated study documentation in compliance with institutional and regulatory requirements.

Requirements

• Bachelor's degree in a related field of study or an equivalent combination of experience and education.
• Experience in a medical and/or research setting.
• Paramedical or other clinical experience.
• Registered Record Administrator preferred.

Responsibilities

• Assists principal investigator and other health professionals in troubleshooting various problems related to the management of the clinical study.
• Assists in all aspects of the data collection process.
• Performs technical procedures on clinical subjects under the direction of the principal investigator or his/her designee.
• Assists with recruitment of patients for the clinical study including tracking the sources of patient referrals.
• Follow-up with sources of patient referrals including referring doctors, various Medical Center labs, and other sources.
• Maintains appropriate patient records as necessary, including charting the condition of the patient and determining their continued eligibility in the study.
• Obtains and interprets pertinent data from medical records as needed to understand past and present condition of the patients.
• Performs day-to-day administrative and clerical duties such as designing brochures, stationery, and data forms.
• Creates reports and graphs pertinent to the study including presentation of the results of the study.
• May supervise other personnel including volunteers as assigned.
• Assists in development of suitable codes and data collection forms for computerization.
• Consults and cooperates with all faculty, coordination centers, sponsors, and health professionals involved in the clinical study.
• Performs other related duties incidental to the work described herein.

Skills

• Understanding of medical and/or scientific terminology.
• Strong oral, written, and interpersonal communication skills.

Work Environment

Clean, well-lit, office environment.

Pay

$24.10 - $36.15 per hour.

Benefits

• Paid Time Off programs.
• Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability.
• Flexible Spending Accounts for eligible health care and dependent care expenses.
• Family benefits such as adoption assistance and paid parental leave.
• Defined contribution retirement plans with employer match and other financial wellness programs.
• Educational Assistance Program.

Note: Eligibility for programs listed above may depend on your FTE or status (e.g., full-time, part-time, per diem, temporary, etc.).