Job Title: Clinical Research Coordinator III (CRC III)
Location: Clifton Schedule: Monday – Friday, 8:00 AM – 5:00 PM
Role Overview We are seeking a highly experienced and autonomous Clinical Research Coordinator III (CRC III) to join our Clifton clinical team. This is a senior-level position designed for a seasoned professional who can hit the ground running without the need for extensive foundational training. You will be entrusted with managing a robust portfolio of complex clinical studies, primarily focusing on Phase I inpatient therapeutic drug trials. If you thrive in a fast-paced clinical environment and have a proven track record of managing multiple interventional trials simultaneously, this role offers the opportunity to work at the cutting edge of clinical research.
Key Responsibilities
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Complex Trial Management: Independently manage and execute 6 to 12 active clinical studies simultaneously, with a primary focus on complex Phase I inpatient trials.
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Patient Coordination: Oversee a fluctuating workload of 10 to 20 active trial patients, handling everything from screening and informed consent to continuous monitoring and follow-up.
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Therapeutic Drug Administration: Apply deep foundational knowledge of therapeutic drug trials to ensure strict protocol adherence, patient safety, and accurate data capture.
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Clinical Operations: Perform hands-on clinical duties, including vital signs, sample processing, and phlebotomy (if credentialed), to support inpatient study requirements.
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Data & Sponsor Management: Maintain immaculate source documentation, manage electronic data capture (EDC), and serve as a reliable point of contact for Principal Investigators and trial sponsors.
Required Qualifications
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Education: High School Diploma or GED minimum.
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Experience: 2 to 3 years of solid, hands-on clinical research experience, specifically with interventional drug trials.
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Capabilities: Proven ability to manage multiple trials and multiple patients concurrently. Must possess the operational maturity to step in and perform immediately.
Preferred Qualifications
Why Join Us? (Selling Points to Talent)
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Cutting-Edge Exposure: Gain highly valuable experience working directly on complex Phase I inpatient trials—a major resume builder for clinical research professionals.
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Autonomy & Trust: Step into a senior role where your expertise is valued. You will be treated as an expert who can drive studies forward without micromanagement.
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Work-Life Balance: Enjoy a highly predictable, Monday-through-Friday daytime schedule (8:00 AM - 5:00 PM), allowing for excellent work-life balance despite the inpatient clinical setting.
Job Title: Clinical Research Coordinator III (CRC III)
Location: Clifton Schedule: Monday – Friday, 8:00 AM – 5:00 PM
Role Overview We are seeking a highly experienced and autonomous Clinical Research Coordinator III (CRC III) to join our Clifton clinical team. This is a senior-level position designed for a seasoned professional who can hit the ground running without the need for extensive foundational training. You will be entrusted with managing a robust portfolio of complex clinical studies, primarily focusing on Phase I inpatient therapeutic drug trials. If you thrive in a fast-paced clinical environment and have a proven track record of managing multiple interventional trials simultaneously, this role offers the opportunity to work at the cutting edge of clinical research.
Key Responsibilities
-
Complex Trial Management: Independently manage and execute 6 to 12 active clinical studies simultaneously, with a primary focus on complex Phase I inpatient trials.
-
Patient Coordination: Oversee a fluctuating workload of 10 to 20 active trial patients, handling everything from screening and informed consent to continuous monitoring and follow-up.
-
Therapeutic Drug Administration: Apply deep foundational knowledge of therapeutic drug trials to ensure strict protocol adherence, patient safety, and accurate data capture.
-
Clinical Operations: Perform hands-on clinical duties, including vital signs, sample processing, and phlebotomy (if credentialed), to support inpatient study requirements.
-
Data & Sponsor Management: Maintain immaculate source documentation, manage electronic data capture (EDC), and serve as a reliable point of contact for Principal Investigators and trial sponsors.
-
Education: High School Diploma or GED minimum.
-
Experience: 2 to 3 years of solid, hands-on clinical research experience, specifically with interventional drug trials.
-
Capabilities: Proven ability to manage multiple trials and multiple patients concurrently. Must possess the operational maturity to step in and perform immediately.
-
Preferred Qualifications
-
Active Phlebotomy certification or strong hands-on phlebotomy experience.
-
Prior experience specifically managing Phase I inpatient trials.
-
Why Join Us? (Selling Points to Talent)
-
Cutting-Edge Exposure: Gain highly valuable experience working directly on complex Phase I inpatient trials—a major resume builder for clinical research professionals.
-
Autonomy & Trust: Step into a senior role where your expertise is valued. You will be treated as an expert who can drive studies forward without micromanagement.
-
Work-Life Balance: Enjoy a highly predictable, Monday-through-Friday daytime schedule (8:00 AM - 5:00 PM), allowing for excellent work-life balance despite the inpatient clinical setting.
-
Required Qualifications
*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.
