Clinical Research Coordinator

Amerit Consulting; San Francisco (CA); On-site; USD 48,216 - 55,104; Full time

Job summary

An established industry player is seeking a Clinical Research Coordinator to oversee various health policy and clinical outcomes studies. This role involves recruiting participants, collecting and managing data, and ensuring adherence to regulatory standards. The ideal candidate will possess strong organizational and communication skills, along with a solid understanding of clinical research protocols. Join a dynamic team dedicated to advancing healthcare research and making a significant impact in the field. If you are passionate about clinical research and thrive in a collaborative environment, this opportunity is perfect for you.

Qualifications

• Experience in clinical research coordination and managing multiple studies.
• Proficiency in data collection and maintaining regulatory documentation.

Responsibilities

• Coordinate clinical research studies and manage participant recruitment.
• Ensure compliance with research protocols and regulatory requirements.

Skills

Clinical Research Coordination

Data Collection

Regulatory Compliance

Participant Recruitment

Communication Skills

Organizational Skills

Education

Bachelor’s degree in biology, public health, psychology, sociology, or related field

Tools

RedCap

Excel

Electronic Medical Records (EMR)

Job description

This range is provided by Amerit Consulting. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$35.00/hr - $40.00/hr

Recruiting Manager/ Lead Engineering Recruiter at Amerit Consulting

Position: Clinical Research Coordinator

Duration: 5-6 Months + Strong Possibility of Extension

Pay Rate: $35/hr - $40/hr (depending on experience)

Job Description

• The Clinical Research Coordinator (CRC) will provide coordination for various health policy, observational, and clinical outcomes studies. The CRC will be responsible for recruiting study participants through screening in person, via Epic, and by phone. They will collect data as required by study protocols from the enrolled participants and assist with IRB submission and other regulatory documentation maintenance.
• The incumbent will support the Department PI under the direction of their supervisor and play a critical role in coordinating clinical research daily operations within the Department of Orthopaedic Surgery.
• Responsibilities include participant confidentiality, timeline management, enrollment, engagement, data/sample collection, and reporting. The CRC will ensure adherence to clinical research protocols and serve as a resource for all aspects of conducting clinical trials. This requires close collaboration with patient care staff, research team members, and study personnel at other sites.
• Study duties include coordination of research protocols, data/specimen collection, and operations of concurrent clinical research studies. The CRC will also be responsible for maintaining databases, managing documentation, and ensuring compliance with all relevant regulations, including Code of Federal Regulations, Good Clinical Practice, and Client policies.

Job Requirements

• Ability to coordinate multiple clinical research studies, including industry-sponsored and investigator-initiated trials.
• Experience in identifying and recruiting study subjects, obtaining informed consent, and conducting patient interviews.
• Proficiency in data collection, database maintenance, and report generation.
• Strong organizational skills to manage regulatory documentation and ensure compliance with all research protocols.
• Knowledge of IRB regulations and experience with protocol submissions and modifications.
• Competence in electronic medical records (EMR) and clinical data management systems.
• Experience in monitoring and reporting adverse events.
• Strong communication and interpersonal skills for collaboration with research teams, patients, and healthcare providers.
• Ability to ensure optimal regulatory compliance for the safe conduct of clinical research.
• Experience working with study sponsors, external agencies, and auditors.

Preferred

• Bilingual proficiency.
• Advanced knowledge of RedCap, Excel, and other clinical research data systems.
• Familiarity with Good Clinical Practice (GCP), HIPAA regulations, and human subject protection policies.
• Bachelor’s degree in biology, public health, psychology, sociology, or related field.
• Two years of experience in a clinical research environment.
• Previous experience in multi-center or complex clinical trials.
• Understanding of billing reconciliation in research settings.
• Ability to develop and maintain case report forms and data collection tools.
• Experience providing training to research staff on study protocols.

Seniority level

Associate

Employment type

Contract

Job function

Research and Science

Industries

Higher Education and Biotechnology Research