Busy Clinical Research and Medical Practice seeking a medical Assistant to assist in coordinating our clinical research studies. Responsible for calling patients, reviewing related study information with then and coordination of clinical schedule, serves as a liaison between the physicians and patient to facilitate the flow of the practice.
Duties and Responsibilities
The primary focus of this role is to assist with the coordination of studies rather than independently managing clinical trials. The position involves coordinating various clinical research projects.
Perform simple study procedures with accuracy – Vitals, ECG, Blood processing and phlebotomy
Follow proper documentation techniques as outlined in the ICH-GCP guidelines – Training will be provided.
Entering medical records into patient database and EMR systems.
Maintain essential regulatory documents as required.
Communicate with study participants by sending study correspondence via mail or email and phone.
Schedule subjects for research visits and follow-up appointments.
Manage study supply inventory – Lab kits, Medication on Site etc.
Work with regulatory support to maintain the regulatory binder.
All Skill will be trained as per our company standards.
Minimum Qualifications
Equivalent in education (medical Assistant certifications etc), training and experience.
Preferred Qualifications
At least 6 months of related experience within a medical clinic setting
Other Requirements
Familiarity with medical terminology.
Ability to communicate effectively with staff and faculty members at all levels.
