Clinical Research Assistant – Trials & Data Support

Mid Atlantic Retina; Shimer (PA); On-site; USD 32,000 - 52,000; Full time

Benefits offered by this job

Hiring incentive – $1,000

Job summary

Mid Atlantic Retina is seeking a Research Assistant to support the Research Unit in conducting clinical trials, data collection and administrative duties. You will assist with patient flow, data entry and regulatory submissions while maintaining accurate records and working closely with physicians and fellows.

This role requires active on-site work, the ability to travel to MAR locations as needed, and a willingness to assist with recruitment and data management tasks in a fast-paced office

Qualifications

• 1 year clinical research experience or ophthalmic experience.

Responsibilities

• Assists the Research Coordinator with the conduction of clinical trials and patient flow.
• Accurately collects clinical data on research patients. Maintains and updates information in data base.
• Assists Coordinator with monitor preparation and follows up on any action items and query resolution.
• Assists in trial recruitment (chart reviews, communicating with Physicians, database reports).
• Aides in regulatory submissions and assists Regulatory Specialist as needed.
• Assists Fellows and Physicians on research projects and data collection.
• Maintains temperature logs for drug closet, freezer and refrigerator. Reports any deviations. Checks and replaces batteries as needed.
• Performs administrative duties for the Research Department including answering phones, scheduling appointments, and ordering supplies.
• Telephone screening of patients.
• Screens research subjects with Coordinator assistance.
• Regular and predictable on-site attendance required.
• Works overtime as needed.
• Travels to other MAR locations as needed.
• Performs other duties as assigned.

Job description

Mid Atlantic Retina is seeking a Research Assistant to support the Research Unit in conducting clinical trials, data collection and administrative duties. You will assist with patient flow, data entry and regulatory submissions while maintaining accurate records and working closely with physicians and fellows.

This role requires active on-site work, the ability to travel to MAR locations as needed, and a willingness to assist with recruitment and data management tasks in a fast-paced office