Position Overview:
This is a full-time Clinical Research Coordinator II opportunity located in Atlanta, Georgia. The CRC II will primarily support Phase II and Phase III clinical trials, managing multiple studies and working closely with the Principal Investigator (PI) and research team.
Typical workload includes approximately 10 active patients and six studies, depending on the research team.
Responsibilities:
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Primarily support Phase II and Phase III clinical trials.
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Manage administrative activities related to the conduct of clinical trials.
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Provide guidance and support to less experienced research staff.
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Manage research databases and develop study-related documents, flow sheets, source documents, and case report forms (CRFs).
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Interact with research participants, determine eligibility, and obtain informed consent according to study protocols.
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Assist with recruitment strategies, patient screenings, interviews, and questionnaires.
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Oversee collection and processing of study specimens.
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Coordinate study procedures, patient scheduling, and other required services.
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Ensure compliance with research protocols and review CRFs for accuracy against source documentation.
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Participate in sponsor monitoring meetings and prepare regulatory submissions.
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May perform phlebotomy or diagnostic procedures with appropriate training and credentials.
Required Skills:
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High School Diploma or GED.
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Clinical Research Coordinator (CRC) experience.
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Must meet one of the following education/experience combinations:
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High School Diploma/GED + 5 years of clinical research experience.
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2 years of college in a scientific, health-related, or business administration program + 3 years of clinical research experience.
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LPN license + 2 years of clinical research experience.
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Bachelor's degree in a scientific, health-related, or business administration program + 1 year of clinical research experience.
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Master's degree, MD, or PhD in a related field.
Preferred Skills:
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Experience with therapeutic drug and interventional clinical trials.
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Experience working in a fast-paced, high-intensity research environment.
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Comfortable working with a very driven, fast-paced Principal Investigator (PI).
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Strong organizational skills and ability to manage multiple studies simultaneously.
Schedule:
Selling Points:
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Opportunity to work with a well-known, established research institution.
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Exposure to Phase II and Phase III clinical trials.
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Opportunity to take ownership of multiple studies and gain experience with complex clinical research responsibilities.
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Opportunity to mentor and support less experienced research staff.
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Work alongside an experienced research team in a well-established clinical research environment.
*We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO), and the California Fair Chance Act (CFCA).
*As a job position within our Clinical Sciences division, a successful completion of a background check may be required as a condition of employment. This requirement is directly related to essential job functions including but not limited to: high-risk working environments (laboratories, clinical settings), handling hazards chemicals or lab specimens, conducting direct patient care, accessing medical and confidential records, access to prescription medication or other drugs, and job duties that can cause serious injury or death as a result of error. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.
