Summary
Experienced candidates with medical backgrounds and excellent interpersonal skills for
the position of Clinical Research Coordinator (CRC). This role is responsible for the successful conduct
of clinical trials under the oversight of the principal investigator. The CRC will be responsible for both
clinical and administrative duties related to the conduct of clinical research at the site.
Responsibilities
Abide by local, state, GCP, ICH and FDA guidelines and regulations for the conduct of clinical trials.
Oversee the smooth running of clinical trials at site in collaboration with study investigator(s) and other team members.
Complete all required organization and study specific training in timely manner, including attendance at offsite investigator meetings.
Supervision and training of site research site staff, including research assistants and lab technicians.
Participate in the planning and conduct of research participant recruitment efforts.
Conduct the proper consent of research participants.
Collecting source obtained from research and transcribe into case report forms.
Perform medically qualified clinical procedures such as vital signs, EKG, and preferably phlebotomy.
Process study labs per requirements.
Collaborate with sponsor/CRO study teams, including prompt resolution of queries and other action items.
Monitoring research participants to ensure adherence to study participation and maintain compliance.
Perform regular inventory checks and ensure the necessary supplies and equipment for a study are in stock and in working order.
QualificationsQualifications
Minimum of 2-3 years of experience in the research field. Preferably on phase II & III studies.
Currently trained or willing to be trained in phlebotomy, performance of vital signs, medical history collection, and administration of EKGs.
Attention to detail.
Exceptional interpersonal and customer service skills.
Outstanding written and verbal communication.
Excellent organizational skill.
Willingness to continually self-educate.
Pluses (but not requirements)
Fluency in Spanish
Skills Required
- Minimum 2-3 years of experience in the research field
- Experience on Phase II and III studies
- Trained or willing to be trained in phlebotomy, vital signs, medical history collection, and EKG administration
- Knowledge of and ability to follow GCP, ICH, and FDA guidelines/regulations for clinical trials
- Ability to obtain informed consent and perform participant recruitment and monitoring
- Experience collaborating with sponsor/CRO study teams and resolving queries
- Attention to detail
- Exceptional interpersonal and customer service skills
- Outstanding written and verbal communication skills
- Excellent organizational skills
- Willingness to continually self-educate
- Fluency in Spanish
What We Do
Cedar Health Research is a multi-therapeutic, independent clinical research site-network and patient network based in Texas. The organization conducts clinical trials and medical research studies aimed at advancing healthcare and improving patient outcomes. By collaborating with pharmaceutical companies, healthcare providers, and patients to evaluate new treatments, it helps bring innovative therapies to market and increases healthcare access through rigorous scientific processes.
