Clinical Studies Coordinator I, Internal Medicine
About The Position
Under general supervision, responsible for the compilation and collection of data, recruitment of subjects, and general coordination of clinical studies. This role involves assisting the principal investigator and other health professionals in troubleshooting study-related problems, performing technical procedures on subjects, maintaining patient records, and interpreting medical data. The position also includes day-to-day administrative and clerical duties such as designing study materials, creating reports and graphs, and potentially supervising personnel. Collaboration with faculty, coordination centers, sponsors, and other health professionals is essential.
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.
- Understanding of medical and/or scientific terminology
- Strong oral, written, and interpersonal communication skills
Nice To Haves
- 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.
- 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, stationary 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.
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
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
