The CRC will be responsible for the conduct and implementation of clinical protocols from pre-study planning through the successful completion of all patient visits and documentation. Appropriate candidate will be responsible for development and implementation of rapid recruitment methods and fulfillment of enrollment goals. Professional interaction and communication with investigators, site personnel, and sponsor clients throughout all stages of the study is a must. Attendance at investigator meetings is expected.
The ideal candidate will be a professional coordinator. Multi-study CRC experience, in a for-profit, performance based, environment is required. CNS experience is a plus. Computer proficiency, excellent clinical, organizational, and time management skills are required. Bilingual English/Spanish is preferred.
Only motivated, self-starters need apply. Applicants must be capable of independently driving their studies.
This is a position that has an opportunity for growth and advancement. Competitive salary based on experience. Medical, Dental and Vision benefits are provided.
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