On-Site Clinical Research Coordinator for Ophthalmology Trials

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

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.