Clinical Research Coordinator Position Available In Duval, Florida

Clinical Research Coordinator

CLINICAL RESEARCH COORDINATOR FULL-TIME

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MONDAY – FRIDAY

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JACKSONVILLE, FL

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BENEFITS PACKAGE

Established in 2001, Southeast Orthopedic Specialists is a regional leader in orthopedic medicine. We are dedicated to growing with our patients. Our reach will continue to expand to meet the needs of all patients, present and future. It is our wish to make industry-leading five-star orthopedic care accessible to as many people as possible. At Southeast Orthopedic Specialists, we are dedicated to taking care of you so you can take care of business! Our robust

BENEFITS PACKAGE

includes the following: Competitive Health & Welfare Benefits
Monthly $43 stipend to use toward ancillary benefits
HSA with qualifying HDHP plans with company match
401k plan
Employee Assistance Program available 24/7
Employee Appreciation Days/Events
Paid Holidays & Paid Vacation As Southeast Orthopedic Specialists continues to grow, we are hiring a Clinical Research Coordinator to support our clinics located in Jacksonville, FL! Please see below for the functions and requirements needed in order to be considered for this position:

GENERAL SUMMARY

Coordinates and oversees clinical or field operation of medical research projects. Participates in assessing, planning, implementing, and evaluating patient care in clinical research studies.

ESSENTIAL FUNCTIONS

Participates in protocol development by drafting study protocols and/or reviewing potential protocols to evaluate their effect on standard clinical procedures; submits to Human Subjects Committee for approval
Recruits study participants by referrals or by placing advertisements on television, radio or in newspapers; schedules appointments, interviews and evaluates potential participants to ensure they meet eligibility requirements; instructs participants concerning protocol and obtains consent signature.
Manages, monitors and participates in research activities including data collection, evaluation and analysis for a research project.
Schedules and/or coordinates the scheduling of required laboratory tests and/or exams
Evaluates and develops patient educational materials and gives patient and/or family members instructions on drug administration and other medical information
Prepares project approval forms necessary for submission to appropriate committees; designs informed consent forms
Trains, oversees and provides current patient information to nurses, medical assistants and other health care personnel in order to assure comprehensive patient care
Prepare and submit initial applications to central and local committees (IRBs, Biosafety, radiology, etc.). Prepares and submit reports as required.
Completes case report forms for each study participant and documents medical data in patient records.
Inventories and requisitions supplies and equipment; arranges for repair and maintenance of equipment
Ensures clinical research compliance with all applicable laws and standards

EDUCATION

Bachelor’s degree AND two years of clinical trial experience

EXPERIENCE

Two plus years experience in the health care field or an equivalent combination of education and experience.
Athletic training experience is desired.

EXPERIENCE

Two plus years experience in the healthcare field or an equivalent combination of education and experience.
Athletic training experience is desired

KNOWLEDGE

Knowledge of computer systems and applications
Knowledge of medical practices, terminology
Knowledge of organizational policies and proceduresKnowledge of the principles, practices, and techniques of nursing care.
Knowledge of clinic policies and procedures
Knowledge of clinical research regulatory guidelines and regulations SKILLS Skill in planning and organizing clinical trials
Skill in evaluating effectiveness of existing methods and procedures
Skill in communicating with internal and external customers

ABILITIES

Ability to communicate clearly and effectively
Ability to set priorities among multiple projects
Ability to interact with providers, clinic and hospital staff

ENVIRONMENTAL WORKING CONDITIONS

Normal office environment.
Some travel within the community.

PHYSICAL/MENTAL DEMANDS

Requires sitting and standing associated with a normal office environment.
Some bending and stretching are required.
Manual dexterity using a calculator and computer keyboard. •This description is intended to provide only basic guidelines for meeting job requirements. Responsibilities, knowledge, skills,
abilities, and working conditions may change as needs evolve. •

QUESTIONS CONTACT HR

@SE-ORTHO.COM Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor. Clinical Research Coordinator Southeast Orthopedic Specialists
Jacksonville, FL
Full Time Published on 05/17/2025