Clinical Research Coordinator

This is a fully remote position, open to applicants in Florida.

📋 Description

• Strategically plan, organize, and oversee resources essential for reaching the objectives and goals of clinical research projects at a single location.

• Coordinate and conduct patient clinical evaluations for trial visits, including scheduling with vendors and other departments or external facilities.

• Execute delegated clinical assessments such as phlebotomy, sample processing, vital signs monitoring, and ECGs following the assigned protocols.

• Liaise with study sponsors, third-party vendors, clinical teams, and patients to ensure that protocol requirements are fulfilled within specified time frames.

• Guarantee site adherence to research protocols.

• Examine case report forms and verify their accuracy against source documents.

• Participate in site monitoring meetings with sponsors.

• Manage site research project databases and create flowsheets and other study-related documentation.

• Complete source documents and case report forms.

• Offer guidance to clinical research personnel and support staff as necessary.

• Suggest procedures to enhance protocol compliance.

• Conduct data entry and resolve queries throughout the assigned trials.

• Act as a resource for internal and external clients and community members regarding clinical research processes.

⛳️ Requirements

• Bachelor's degree in a relevant field OR a comparable combination of education and experience.

• A minimum of two (2) years of related experience is preferred.

• Level II background check is mandatory.

• Must fulfill all employment eligibility criteria in the U.S.

🏝️ Benefits

• Medical, dental, and life insurance plans.

• Retirement plan options.

• Tuition programs for employees and dependents.

• Generous leave policies.

• A wide array of employee perks and discounts.