Clinical Research Coordinator Position Available In Duval, Florida
Tallo's Job Summary: Southeast Orthopedic Specialists in Jacksonville, FL is seeking a Clinical Research Coordinator to oversee medical research projects, recruit participants, manage data collection, and ensure compliance with regulations. The role requires a Bachelor's degree, two years of clinical trial experience, and knowledge of medical practices and terminology. Competitive benefits package included.
Job Description
CLINICAL RESEARCH COORDINATOR FULL-TIME
|
MONDAY – FRIDAY
|
JACKSONVILLE, FL
|
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 C linical 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
