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Headlands Research
Overview
The CRC manages Phase II-IV clinical studies from initiation to close-out, ensuring compliance with FDA and GCP guidelines. Key duties include conducting subject visits, managing recruitment, and maintaining accurate clinical documentation.
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Compensation
Salary not listed
Posted
8 days ago
The coordinator is responsible for managing all aspects of research protocols to ensure integrity and quality according to GCP guidelines. Key duties include performing visit procedures, managing study supplies, and providing high-level care to study patients.
$70,000 - $75,000 / YEAR
9 days ago
The Sub-Investigator will ensure the safety and welfare of study subjects by maintaining in-depth knowledge of all research protocols, screening subjects, conducting medical interviews and exams, reviewing results, and providing necessary medical care during trials. Responsibilities also include providing home-based on-call availability and attending Investigator Meetings when required.
Key responsibilities involve preparing and administering specialized therapies, including IV infusions, monitoring study participants, and thoroughly documenting all clinical activities to support operational and clinical objectives. The role also requires conducting intake procedures, performing cognitive assessments, and maintaining clear communication to ensure participant safety and protocol compliance.
