RETINA CONSULTANTS OF DELMARVA, P.A.
Clinical Research Coordinator
RETINA CONSULTANTS OF DELMARVA, P.A., Salisbury, Maryland, United States, 21801
RETINA CONSULTANTS OF DELMARVA, P.A. is a distinguished medical practice located in Salisbury, Maryland, specializing in providing expert care in retinal health. Based at 6511 Deer Pointe Drive, the practice is dedicated to delivering high-quality medical services to its community. The organization prioritizes patient-centered care and works diligently to address various retinal conditions with advanced treatment options.
Role Description This is a full-time, on-site Clinical Research Coordinator role based in Salisbury, MD. The Clinical Research Coordinator will be responsible for managing clinical trial protocols, obtaining informed consents, coordinating and conducting research activities, and ensuring compliance with all clinical trial regulations and standards. Responsibilities also include liaising with clinical teams, sponsors, and regulatory bodies to ensure successful execution of clinical studies.
Qualifications
Proficient knowledge of Informed Consent processes and practices
Experience and understanding of Clinical Research and Clinical Trials
Expertise in creating and managing study Protocols and associated requirements
Previous experience in clinical research (Clinical Research Experience preferred)
Strong organizational and decision‑making skills
Ability to effectively collaborate with multidisciplinary teams
Bachelor's degree in a health‑related field or equivalent experience
Familiarity with regulatory standards and clinical data management practices
Ensure adherence to GCP, IRB, and FDA guidelines
Prior clinical research or healthcare experience preferred (ophthalmology experience a plus, but not required)
Salary: Competitive wage starting at $49,000–$60,000, with opportunities for increases based on productivity and performance.
Schedule: Somewhat flexible schedule
Start Date: Immediate start preferred
Seniority level
Entry level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Medical Practices
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Role Description This is a full-time, on-site Clinical Research Coordinator role based in Salisbury, MD. The Clinical Research Coordinator will be responsible for managing clinical trial protocols, obtaining informed consents, coordinating and conducting research activities, and ensuring compliance with all clinical trial regulations and standards. Responsibilities also include liaising with clinical teams, sponsors, and regulatory bodies to ensure successful execution of clinical studies.
Qualifications
Proficient knowledge of Informed Consent processes and practices
Experience and understanding of Clinical Research and Clinical Trials
Expertise in creating and managing study Protocols and associated requirements
Previous experience in clinical research (Clinical Research Experience preferred)
Strong organizational and decision‑making skills
Ability to effectively collaborate with multidisciplinary teams
Bachelor's degree in a health‑related field or equivalent experience
Familiarity with regulatory standards and clinical data management practices
Ensure adherence to GCP, IRB, and FDA guidelines
Prior clinical research or healthcare experience preferred (ophthalmology experience a plus, but not required)
Salary: Competitive wage starting at $49,000–$60,000, with opportunities for increases based on productivity and performance.
Schedule: Somewhat flexible schedule
Start Date: Immediate start preferred
Seniority level
Entry level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Medical Practices
#J-18808-Ljbffr