Job detail

Clinical Research Coordinator

PRIME CLINICAL RESEARCH INC

#Regulatory Requirements #Microsoft Office Suite #GCP #Life Sciences #Data Collection #Patient Outcomes #Informed Consent #Regulatory Agencies #Ethics Committees

Quick overview

The Clinical Research Coordinator manages clinical trial activities, including participant recruitment, screening, and enrollment while ensuring strict adherence to study protocols. They also monitor patient progress, collect trial data, and facilitate communication between investigators, sponsors, and regulatory bodies.

Requirements summary

Candidates should have a bachelor's degree in life sciences or a related field and previous experience in clinical research. Strong knowledge of Good Clinical Practice (GCP) and regulatory requirements is essential for this role.

bachelor degreeprofessional certificateAttention To DetailCommunicationOrganizational SkillsMentoringRegulatory ComplianceMicrosoft Office SuiteData CollectionClinical ResearchPatient RecruitmentInformed ConsentGood Clinical PracticeClinical Trial ManagementProtocol Management

Job description

About the Role

Join PRIME CLINICAL RESEARCH INC as a Clinical Research Coordinator in Mansfield, TX, where you'll play a vital role in advancing medical research. This exciting position offers the opportunity to work on innovative clinical trials while collaborating with a passionate team dedicated to improving patient outcomes.

Responsibilities

Coordinate and manage clinical trial activities to ensure compliance with study protocols. Recruit, screen, and enroll study participants while maintaining accurate records. Conduct informed consent discussions and provide education to participants. Monitor patient progress and collect data throughout the trial phases. Collaborate with investigators and regulatory bodies to ensure adherence to guidelines. Prepare and submit necessary documentation to ethics committees and regulatory agencies. Facilitate communication between study participants, sponsors, and team members. Assist in the training and mentoring of new staff members as needed.

Requirements

Bachelor’s degree in life sciences or a related field preferred. Previous experience in clinical research or as a clinical research coordinator. Strong knowledge of Good Clinical Practice (GCP) and regulatory requirements. Excellent organizational skills and attention to detail. Effective communication and interpersonal skills to work with diverse teams. Ability to manage multiple tasks and meet deadlines in a fast-paced environment. Certification in Clinical Research (e.g., ACRP or SOCRA) is a plus. Proficient in Microsoft Office Suite and clinical trial management software. About Us: PRIME CLINICAL RESEARCH INC has been at the forefront of clinical research in DFW Area, dedicated to delivering high-quality results for our clients. Our commitment to innovation and excellence has made us a trusted partner in the industry, while our supportive work environment fosters career growth and employee satisfaction.