Clinical Research Coordinator II

Care Access; St. Louis (MO); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Paid Time Off (PTO)

100% Employer paid medical, dental, and vision insurance

401(k) Retirement Plan with Company Match

Job summary

Care Access is looking for a Clinical Research Coordinator in St. Louis, Missouri, to oversee clinical trials. This role requires adherence to GCP and FDA regulations while screening and monitoring study subjects.

The ideal candidate will have at least 3 years of experience and be proficient in medical terminology. Excellent communication skills and the ability to work in a fast-paced environment are essential. A Bachelor's degree is preferred.

Benefits include medical insurance, PTO, and a 401(k) plan with a company match.

Qualifications

• Minimum of 3 years prior Clinical Research Coordinator experience required.
• Recent phlebotomy experience required.
• Ability to work independently in a fast-paced environment.

Responsibilities

• Utilize GCP for screening and monitoring clinical research study subjects.
• Maintain relationships with study participants and Care Access Research personnel.
• Document data accurately on paper or e-source documents.

Skills

Understanding of Good Clinical Practices (GCP)

Excellent knowledge of medical and research terminology

Strong communication skills

Organizational and prioritization skills

Critical thinking

Education

Bachelor’s Degree or equivalent combination of education, training and experience

Tools

Clinical trials database

IVR systems

MS Word and Excel

Job description

Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world‑class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow.

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.

The Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCP) in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.

How You'll Make An Impact

• Prioritize activities with specific regard to protocol timelines
• Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials.
• Maintain effective relationships with study participants and other Care Access Research personnel.
• Balance protocol needs with patient experience; proactively address concerns.
• Interact in a positive, professional manner with patients, representatives, investigators and Care Access Research personnel and management.
• Coordinate and attend pre‑study site visits, site initiation visits, and monitor visits with clinical staff and Sponsor/CRO representatives.
• Mentor CRC I peers; provide onboarding and day‑to‑day guidance.
• Identify adverse events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor (where appropriate)
• Moderate complexity; mixed visit types, active IP and AE/SAE workflows.
• Obtain informed consent per Care Access Research SOP.
• Complete visit procedures in accordance with protocol.
• Complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc.
• Review laboratory results, ECGs, and other test results (e.g., MRIs) for completeness and alert values, ensuring investigator review in a timely fashion.
• Discuss study medication, required procedures, eligibility criteria and impact on office flow with Investigator and site staff.
• Documentation
  • Record data legibly and enter in real time on paper or e‑source documents
  • Accurately record study medication inventory, medication dispensation, and patient compliance.
  • Resolve data management queries and correct source data within sponsor provided timelines
  • Assist regulatory personnel with completion and filing of regulatory documents.
  • Assist in the creation and review of source documents.
• Assist with planning and creation of appropriate recruitment materials.
• Assist in the development of recruitment plan and obtain listing of potential candidates to contact from subject database.
• Actively work with recruitment team in calling and recruiting subjects
• Review and assess protocol (including amendments) for clarity, logistical feasibility
• Ensure that all training and study requirements are met prior to trial conduct.
• Communicate clearly verbally and in writing.
• Anticipate needs; propose solutions; manage change effectively.
• Attend Investigator meetings as required.
• Ensure adequate supplies have arrived on site for protocol initiation (lab kits, study medication, specialized equipment, IVRS/EDC access and passwords)

Expertise Required

• Ability to understand and follow institutional SOPs.
• Excellent working knowledge of medical and research terminology
• Excellent working knowledge of federal regulations, good clinical practices (GCP)
• Operate independently for most study activities; escalates complex issues as needed.
• Ability to communicate and work effectively with a diverse team of professionals.
• Strong organizational, prioritization and leadership skills with a strong attention to detail
• Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel.
• Critical thinker and problem solver
• Friendly, outgoing personality; maintain a positive attitude under pressure.
• High level of self‑motivation and energy
• Excellent professional writing and communication skills
• Manages stakeholder communications; facilitates visits and meetings.
• Ability to work independently in a fast‑paced environment with minimal supervision.

Certifications, Licenses, Education, and Experience

• Bachelor’s Degree preferred, or equivalent combination of education, training and experience.
• A minimum of 3 years prior Clinical Research Coordinator experience required.
• Prefer 1 year of experience as a Care Access Research Clinical Research Coordinator.
• Recent phlebotomy experience required.

Location and Travel

• Location: This is an on‑site position with regional commute requirements.
  • Travel: This role requires up to 10% travel. Length of travel will depend upon study requirements, staff needs, and company initiatives.
    • Type of travel required: Regional (within 100 miles)
  • Physical demands associated with this position include:
    • Walking, standing, sitting, lifting (up to 25 lbs and overhead), driving - 20%

The expected salary range for this role is $60,000 - $90,000 USD per year for full time team members.

Benefits & Perks (US Full Time Employees)

• Paid Time Off (PTO) and Company Paid Holidays
• 100% Employer paid medical, dental, and vision insurance plan options
• Health Savings Account and Flexible Spending Accounts
• Bi‑weekly HSA employer contribution
• Company paid Short‑Term Disability and Long‑Term Disability
• 401(k) Retirement Plan, with Company Match
• Relocation Support Provided

We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Care Access is unable to sponsor work visas at this time.

Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction.

Notice to Connecticut applicants: Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment.

Notice to Arizona, Georgia, Indiana, and North Dakota applicants: Care Access complies with applicable laws prohibiting smoking in and around places of employment.

Notice to Massachusetts applicants: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Notice to Rhode Island applicants: Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment.

Notice to Maryland applicants: Under Maryland law, an employer MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100.