Clinical Research Coordinator

CLINICAL RESEARCH COORDINATOR

FULLTIME MONDAY FRIDAY JACKSONVILLE FL BENEFITS PACKAGE

Established in 2001Southeast Orthopedic Specialistsis 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 industryleading fivestar orthopedic care accessible to as many people as possible.

AtSoutheast Orthopedic Specialists we are dedicated to taking care of you so you can take care of business! Our robustBENEFITS PACKAGEincludes 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

AsSoutheast Orthopedic Specialistscontinues to grow we are hiringa 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 drugadministration 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 inorder to assure comprehensive patient care

• Prepare and submit initial applications to central and local committees (IRBs Biosafety radiology etc.). Prepares andsubmit 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

• Bachelors 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

Required Experience:

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