Research Coordinator

Would you be interested in furthering your healthcare career with an innovative company where you can be of help to those in need of wound care? If you are dependable and efficient, have current CPR certification, and would want to be part of a team of professionals who provide high-quality care for patients with complex medical conditions, WoundCentrics wants you on board as a Research Coordinator.

As a Clinical Research Coordinator with WoundCentrics, you would promote and restore the patient's health by completing the research process; collaborating with the physician and multi-disciplinary team members and provide physical and psychological support to patients and guardians caring for the patient. Here, you can grow an amazing career through ongoing training, plus enjoy enviable benefits and perks that include a full benefits package and a schedule of Monday through Friday 8a-5p that will allow you a healthy work/life balance - not to mention no on-call!

If you have a desire to improve lives and would want to be part of a clinically focused company that is an industry leader in wound care, apply for the clinical research coordinator position with WoundCentrics today!

Job Summary:

The Clinical Research Coordinator (CRC) is responsible for managing and coordinating clinical research studies under the supervision of a Principal Investigator (PI). This role ensures compliance with regulatory requirements, study protocols, and institutional policies. The CRC will interact with study participants, collect and manage data, and maintain study documentation to ensure the integrity and success of clinical trials.

Responsibilities:

• Coordinate and manage day-to-day clinical trial operations.
• Recruit, screen, and enroll study participants.
• Obtain informed consent and ensure participants meet eligibility criteria.
• Schedule and conduct study visits according to protocol timelines.
• Collect, process, and ship biological samples as required.
• Maintain accurate and complete source documentation and case report forms (CRFs).
• Ensure compliance with ICH-GCP guidelines, FDA regulations, and institutional SOPs.
• Communicate with sponsors, CROs, IRBs, and other stakeholders.
• Assist with budget tracking and study billing.
• Participate in monitoring visits and audits.
• Provide regular updates to investigators and clinical teams. 

Qualifications:

• Bachelor’s degree in a health or science-related field required; Master’s preferred.
• At least 1-2 years of experience in research (clinical setting preferred) or healthcare setting.
• Knowledge of clinical trial processes, GCP, and regulatory requirements.
• Certification (e.g., SOCRA or ACRP) preferred but not required.
• Strong organizational and communication skills.
• Proficient in Microsoft Office and EDC systems.
• Bilingual (English/Spanish) preferred
• Phlebotomy experience is a plus!

Other Requirements

• Prolonged periods of sitting or standing.
• Exert 20-50 lbs. of force occasionally and 10-20 lbs. frequently.
• Exposure to biological samples and clinical environments.
• Must be able to travel locally between study sites if required.Bottom of Form