Position Summary
The Clinical Research Coordinator (CRC) will provide support for research activities in the Metabolic Bone Diseases Unit.
Reporting to the Principal Investigator, the CRC will assist with recruitment, assessment and follow up in research studies.
Responsibilities
- Responsible for participant recruitment, assessment and follow-up for a cohort study
- Provide back-up support for clinical trials including working with other study personnel, performing data collection, screening and recruitment of study participants
- Assist with patient education, obtain informed consent and dispense study drug
- Prepare and maintain manual of operations and create study questionnaires
- Assist with preparation of documents for renewals, modifications, yearly submissions, and correspondence to IRB as wells as for audits
- Assure compliance with study protocol and resolve queries
- Extract data from patient charts and develop ongoing reports for Principal Investigator, statistician and DSMC
- Assist in the preparation of submissions for scientific conferences and manuscripts
- Assist with financial tracking and confirmation of invoices for study related expenses (taxi vouchers, lab and study material supplies)
- Responsible for inventory and procurement of laboratory and office supplies
- Perform additional related duties as needed
Minimum Qualifications
- Bachelor’s degree or equivalent in education, training and experience.
- Excellent verbal and written communication skills
- Attention to detail with ability to work effectively with minimal supervision
- Computer skills (Word, Excel) required
Preferred Qualifications
- Bilingual (English and Spanish) language skills
- Experience in the administration of clinical trials
- Phlebotomy certification
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