Clinical Research Coordinator (San Diego, CA)*

Profound Research LLC; Carlsbad (CA); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Health insurance

PTO

Retirement plan

Professional development support

Job summary

Medium is seeking a Clinical Research Coordinator in Carlsbad, California, responsible for conducting and managing clinical trial activities while ensuring compliance with protocols and regulations. Candidates should have a bachelor's degree and relevant experience in the life sciences, with GCP certification to be completed within six months. The role involves mentoring staff, managing study operations, and requires excellent communication skills. Benefits include competitive compensation, health insurance, PTO, and retirement plans.

Qualifications

• Bachelor’s degree with 2 years relevant experience in life sciences or equivalent.
• Must complete GCP and CCRC certification within 6 months of hire.
• Capacity to work independently and manage time effectively.

Responsibilities

• Manage clinical trial activities according to research protocols.
• Mentor and train staff on clinical trial management.
• Coordinate all aspects of assigned clinical trials.

Skills

Clinical Research Coordinator experience

Ability to communicate effectively

Attention to detail

Teamwork skills

Proficient in clinical assessments

Education

Bachelor's degree in life sciences

Associate's degree with relevant experience

High School Graduate with sufficient experience

Job description

Responsibilities

• Conduct and manage all clinical trial activities in accordance with established research protocols and standards in compliance with all applicable laws, regulations, policies, and procedural requirements.
• Complete all relevant Profound Research required training, including but not limited to ICH‑GCP certification and IATA certification in a timely manner.
• Mentor and train staff in the conduct of clinical trials, protocol requirements, communication and trial management skills.
• Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start‑up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, deviations, and monitoring visits and follow‑up.
• Ensure good documentation practices are applied by all team members when collecting, maintaining and correcting study data and required records of clinical trial activity including but not limited to source documentation, case report forms, queries, drug dispensation records, and regulatory forms.
• Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.
• Collect and account for supplies from sponsors such as lab kits, ancillary supplies, and investigational products.
• Other duties as assigned.

Requirements

• Bachelor’s degree and 2 years relevant experience in the life science industry OR
• Associate’s degree with 4 years relevant experience in the life science industry OR
• High School Graduate and/or technical degree with minimum of 6 years relevant experience in the life science industry AND 1 year
• Clinical Research Coordinator experience
• Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification within 6 months of being in the role
• Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
• Proficient ability to work independently, plan and prioritize with minimal guidance
• Excellent attention to detail, organization, and communication with varied stakeholders
• Ability to work as a team player with the ability to adapt to changing schedules and assignments

Travel Requirements

Daily commute to site(s)

Physical Requirements & Work Environment

This role is primarily performed in a remote/office environment and requires prolonged periods of sitting or standing at a desk, working on a computer, and participating in virtual meetings.

Requires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials.

Minimal travel to company sites, meetings, or partner locations may be required, including the ability to navigate office/clinical environments and transport typical work materials.

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role.

Benefits

Competitive compensation, health insurance, PTO, retirement plan, and professional development support.