Travel Study Coordinator 248870

Medix™; United States; Remote; USD 75,000 - 80,000; Full time

Benefits offered by this job

Travel costs covered

Daily meal per diem

Job summary

A healthcare-focused company is seeking a Clinical Research Coordinator for an exciting opportunity that involves managing daily clinical trial activities. This role will primarily be remote, requiring up to 70% travel across the US. Candidates should possess a Bachelor’s Degree and ideally have experience in ophthalmology. Responsibilities include training staff, ensuring compliance, and data management. This position offers competitive compensation and covers all travel expenses.

Qualifications

• Must have a Bachelor’s Degree or 3 years’ experience as a clinical research coordinator with industry experience.
• Ophthalmology experience preferred.
• CCRC certification preferred.

Responsibilities

• Facilitates daily clinical trial activities of the study.
• Trains study staff and documents the training.
• Enters data into the electronic data capture (EDC) system.
• Coordinates monitor site visits and prepares documentation.

Skills

Ophthalmology experience

Clinical trial coordination

Regulatory compliance

Education

Bachelor’s Degree

Job description

Base pay range

$75,000.00/yr - $80,000.00/yr

We are looking for a seasoned Clinical Research Coordinator who is interested in jumping into an exciting opportunity with a growing team that is an integral part of a large national network of sites. This role will be based remotely on either the West or East coast and will require up to 70 percent weekly travel to various sites to work as a Study Coordinator.

Weekend travel is not anticipated; all travel costs are covered along with a daily meal per diem and candidates must live within a half hour of a major US airport.

Must haves

• Bachelor’s Degree and/or 3 years’ experience as a clinical research coordinator with industry experience
• Ophthalmology experience preferred
• CCRC Preferred

Responsibilities

• Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study
• Ensures study staff is properly trained on study-related information (i.e., protocol, ICF, manuals, etc.) and that the training is documented
• Attends teleconferences and Investigator Meetings as requested by research director
• Reviews and comprehends all study protocols, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, and privacy protections
• Collects updated medical history, adverse events and serious adverse events that need to be reported to the sponsor and IRB within required time frame
• Assures that amended consent forms are appropriately implemented and signed
• Acts as a secondary reviewer to provide oversight so that the ICF process is conducted accurately
• Collects data as required by the protocol and enters information into the electronic data capture (EDC) system in the specified time frame indicated in the study contract.
• Oversees data and ensures that it is being entered correctly and resolves any queries issued within required time frame
• Responsible for ensuring all SUSAR/Safety Reports are acknowledged and reviewed
• Coordinates monitor site visits and assists with preparation of site visit documentation
• Works with the monitor to make any corrections needed to meet requirements and deadlines as needed
• Manages and maintains all regulatory information about the study including the protocol, investigator brochure, IRB documents, Investigator disclosures, CVs, training documentation, instructions on reporting requirements for the IRB and the sponsor