What are the responsibilities and job description for the Research Assistant position at Cedar Health Research?
Job Details
Ft Worth, TX Full Time
Description
Description
Experienced candidates with familiarity to medical/research backgrounds and excellent interpersonal skills for the position of Research Assistant (RA). This role supports Clinical Research Coordinators (CRCs) in their daily activities of carrying out clinical trials under the oversight of the principal investigator. The RA 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.
Overseeing the smooth running of clinical trials at site in collaboration with CRCs, study investigator(s) and other team members.
Complete all required organization and study specific training in timely manner.
Assisting with conduct of research study and GCP practices.
Setting up rooms for patient visits, request medical records, follow-up phone calls to patients, etc.
Collecting source obtained from research and transcribe into case report forms.
Willingness to learn clinical procedures such as vital signs, EKG and phlebotomy.
Process study labs per requirements.
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.
Engaging with subjects and understanding their concerns.
Qualifications
Qualifications
2 years’ experience as a medical assistant or research assistant.
Currently trained or willing to be trained in phlebotomy, vaccine administration, 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
Fluency in Spanish
Ft Worth, TX Full Time
Description
Description
Experienced candidates with familiarity to medical/research backgrounds and excellent interpersonal skills for the position of Research Assistant (RA). This role supports Clinical Research Coordinators (CRCs) in their daily activities of carrying out clinical trials under the oversight of the principal investigator. The RA 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.
Overseeing the smooth running of clinical trials at site in collaboration with CRCs, study investigator(s) and other team members.
Complete all required organization and study specific training in timely manner.
Assisting with conduct of research study and GCP practices.
Setting up rooms for patient visits, request medical records, follow-up phone calls to patients, etc.
Collecting source obtained from research and transcribe into case report forms.
Willingness to learn clinical procedures such as vital signs, EKG and phlebotomy.
Process study labs per requirements.
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.
Engaging with subjects and understanding their concerns.
Qualifications
Qualifications
2 years’ experience as a medical assistant or research assistant.
Currently trained or willing to be trained in phlebotomy, vaccine administration, 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
Fluency in Spanish
