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 and Holidays

100% Employer-paid medical, dental, &

Health Savings Account and Flexible SP

Bi-weekly HSA employer contribution

Disability insurance (short & long)

401(k) with company match

Relocation support

Job summary

Care Access is hiring a Clinical Research Coordinator to ensure GCP-compliant screening, enrollment and monitoring of study subjects across clinical trials. The role emphasizes regulatory adherence and strong patient relations, working with diverse teams.

You'll coordinate site visits, manage data entry, and support recruitment efforts, with opportunities to mentor junior CRC staff and contribute to study success.

Qualifications

• Bachelor’s degree preferred or equivalent experience.
• 3 years prior Clinical Research Coordinator experience required.
• Recent phlebotomy experience required.

Responsibilities

• Screen, enroll, and monitor study subjects per protocol and GCP.
• Maintain FDA regulations and ICH guidelines across trials.
• Foster effective relationships with participants and study staff.
• Coordinate site visits and manage regulatory documents.
• Mentor CRC I peers and support onboarding.
• Identify AEs/SAEs and report to PI and Sponsor as needed.
• Assist in recruitment planning and materials development.
• Ensure training is completed prior to trial conduct.

Skills

GCP knowledge

Regulatory compliance

Communication skills

Attention to detail

Leadership

Education

Bachelor’s Degree preferred

Tools

Clinical trials database

IVR systems

Electronic data capture

MS Word

MS 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 likeFuture of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, andDifference 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)s 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.
• Balances protocol needs with patient experience; proactively addresses 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.
• Mentors CRC I peers; provides 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 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.
• Anticipates needs; proposes solutions; manages 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)

The 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)
• Operates 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 and capabilities 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.
• 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

How We Work Together

• Location: This is an on-site position with regional commute requirements
  • Travel: This role requires up to 10% travel requirements further explained below. 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: The ability to use keyboards and other computer equipment.
  
  • Walking - 20%
  • Standing - 20%
  • Sitting - 20%
  • Lifting - 20%
    • Up to 25lbs
    • Over 25lbs Overhead
  • Driving - 20%

The expected pay 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

Mandatory Employer Disclosures

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. Care Access is also subject to is subject to Chapters 29–38 of Title 28 of the Rhode Island General Laws.
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