Clinical Research Coordinator

RETINA CONSULTANTS OF DELMARVA, P.A.; Salisbury (MD); On-site; USD 49,000 - 60,000; Full time

Benefits offered by this job

Competitive wage

Opportunities for increases based on productivity

Somewhat flexible schedule

Job summary

A distinguished medical practice in Salisbury, MD is looking for a Clinical Research Coordinator. This full-time role involves managing clinical trial protocols, obtaining informed consents, and ensuring compliance with regulations. Candidates should have a Bachelor’s in a health-related field, and experience in clinical research is preferred. The salary range is $49,000 to $60,000 with flexible scheduling and opportunities for growth based on performance.

Qualifications

• Strong decision-making skills and ability to manage protocols.
• Ensure adherence to GCP, IRB, and FDA guidelines.
• Previous clinical research experience preferred.

Responsibilities

• Manage clinical trial protocols and obtain informed consents.
• Coordinate and conduct research activities.
• Liaise with clinical teams and sponsors for successful execution.

Skills

Proficient knowledge of Informed Consent processes

Experience in Clinical Research and Clinical Trials

Expertise in creating and managing study Protocols

Strong organizational skills

Ability to collaborate with multidisciplinary teams

Familiarity with regulatory standards

Education

Bachelor's degree in a health-related field

Job description

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