What are the responsibilities and job description for the Clinical Research Coordinator position at Morph Enterprise?
Job Title :- Clinical Research Coordinator
Location :- Los Angeles, CA
Duration :- 13 weeks
Shift :- Days
Job Description :-
Primary Duties and Responsibilities
* Establishes and executes logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety.
* Coordinates administrative functions of research studies, including scheduling of patients for research visits, procedures and labs and completion and maintenance of consent forms, case report forms, SAE’s and source documents.
* Responsible for screening and recruitment of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and supporting the informed consent process.
* Responsible for accurate and timely data collection, documentation, entry and reporting, including resolution of queries from sponsors or regulatory entities.
* Coordinates institutional, pharmaceutical and internal audits, including facilitating third party study monitoring and designs and implements needed corrective actions.
* Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.
Required:
* Associates Degree
* 3 years of Clinical Research Experience
* BLS
Preferred:
* Bachelors Degree
* SoCRA or ACRP Certification
* Phlebotomy Certified
* Medical Assistant Diploma
* Experience with Oncology setting
Note :- Feel free to share a reference for above role. We have a great referral policy if your reference completes the projects of employment with client.
Salary : $43 - $46
