Clinical Research Coordinator Position Available In Orange, Florida
Tallo's Job Summary: The Clinical Research Coordinator position at Conquest Research in Winter Park, FL involves coordinating clinical studies, assessing patient eligibility, and managing protocol procedures. A 2-year degree and 2 years of clinical research experience are required. The role offers a competitive salary range of $55,000 to $65,000 per year, full-time hours, and comprehensive benefits.
Job Description
Clinical Research Coordinator Conquest Research 2233 Lee Road, Winter Park, FL 32789
POSITION:
The Clinical Research Coordinator participates in the development, coordination and implementation of research and administrative strategies essential to the management of clinical trials research.
EDUCATION AND EXPERIENCE
Minimum 2-year degree necessary Two (2) years of clinical research or healthcare experience required
RESPONSIBILITIES
Coordinate Clinical Studies Assesses patients for protocol eligibility and communicates findings to investigator/physician Coordinates the implementation of protocol procedures Collect initial medical background from patients and other appropriate sources Work as a cohesive team member coordinating assigned studies and backing up other studies on location Educate and provide information to patients, families, and community groups regarding clinical drug trials Assist and support Recruitment Team with prescreen activities and other related activities Attend Study related training and site initiation meetings Inventory, handle, and maintain accountability for all study supplies and investigational products Facilitate study monitoring visits and prompt resolution of all study related queries Maintain professional and appropriate interactions with sponsors and all other study related personnel, subjects, families, and staff members Assesses and monitors patient responses and adverse reactions; reports to accountable sources Completes a variety of reports, documents and correspondence for regulatory agencies, participating clinical trial sites and for internal purposes Collaborates with physicians and other healthcare staff to ensure adherence to FDA and protocol guidelines; identify potential problems and/or inconsistencies and take action as appropriate Assist in the preparation and submission of amendments to clinical trials protocols to the IRB Other duties as assigned PAY This position provides a base salary and incentive plan.
SCHEDULE
Monday – Thursday 8:00a-5:00p Friday 8:00a-12:00p
QUALIFICATIONS AND SKILLS
Commitment to excellence and quality patient care High organizational ability with strong attention to detail Critical thinker and problem solver Excellent phlebotomy and IV skills are also a major asset Intermediate computer skills needed
BENEFITS
Competitive compensation Comprehensive benefits package including: Medical, dental, vision, life, and disability insurance Paid time off Holiday pay 401(k) with company match
Job Type:
Full-time Pay:
$55,000.00 – $65,000.00 per year
Benefits:
401(k) 401(k) matching Dental insurance Health insurance Health savings account Life insurance Paid time off Professional development assistance Vision insurance
Schedule:
8 hour shift Monday to
Friday Education:
Bachelor’s (Required)
Experience:
Clinical research: 1 year (Preferred) Ability to
Commute:
Winter Park, FL 32789 (Required)
Work Location:
In person
