Clinical Research Coord - Day - Full time - Corp (Traveling to diff. Locations)

Position Summary:

Department:OHJOI Research & Education  
Shift: Day with flexability M-F /Full Time    

Location: Four Courners, Hunters Creek and Horizon West (NOT a Remote Role)

Title: Clinical Research Coord I 

Summary: Participate in the development, coordination and implementation of research and administrative strategies essential to the management of clinical trials research. 

 

“Orlando Health Is Your Best Place to Work” is not just something we say, it’s our promise to you.”

Orlando Health proudly embraces and honors the individuality of our team members. By sharing different ideas and perspectives and working together as a team, we are better able to relate to, care for and authentically serve our patients and families who make up the collective populations in our community. So, no matter who you are, what you believe or how you express yourself, you are welcome here.

ORLANDO HEALTH - BENEFITS & PERKS:

Competitive Pay

• Evening, nights, and weekend shift differentials offered for qualifying positions.

All Inclusive Benefits (start day one)

• Student loan repayment, tuition reimbursement, FREE college education programs, retirement savings, paid paternity leave, fertility benefits, back up elder and childcare, pet insurance, PTO/Holidays, and more for full time and part time employees.

Forbes Recognizes Orlando Health as a Best-In-State Employer

• Forbes has named Orlando Health as one of America's Best-In-State Employers for 2021. Orlando Health is the top healthcare organization in the Metro Orlando area to make the prestigious list. "We are proud to be named once again as a best place to work," said Karen Frenier, VP (HR). "This achievement reflects our positive culture and efforts to ensure that all team members feel respected, supported and valued.

Employee-centric

• Orlando Health has been selected as one of the “Best Places to Work in Healthcare” by Modern Healthcare.

Responsibilities:

Essential Functions
 Participate in the coordination of multi-site or large-scale clinical trials research studies conducted by a supervising principal investigator(s) in support of activities that meet objectives of assigned research protocol(s).
 Assesses patients for protocol eligibility and communicates findings to investigator/physician.
 Coordinates the implementation of protocol procedures.
 Operates specialized equipment as needed in assigned area, if applicable.
 Assesses and monitors patient responses and adverse reactions; reports same to accountable sources.
 Provides appropriate patient and family education.
 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.
 Provides educational in-services as needed.
 Promotes interdepartmental cooperation and coordination for each protocol.
 Maintains reasonably regular, punctual attendance consistent with Orlando Health policies, the ADA, FMLA and other federal, state, and local standards.
 Maintains compliance with all Orlando Health policies and procedures.
Other Related Functions
 Assists in the development of treatment orders for active studies, to be reviewed by the treating physician.
 Assists the research team in preparing for site audits.
 Attends appropriate departmental and/or corporate meetings.
 Attends study group and investigator meetings as required.
 Demonstrates ability in using computer software specific to department.
 Support the team of data managers by answering complex questions and entering information into the EDC if necessary.

Qualifications:

Must meet one of the following:

• Bachelor’s degree in health-related field (i.e., Healthcare Administrative, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management); or
• Associate degree in related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management) and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section); or
• Graduate of an accredited allied health program and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section).

If no degree, experience may be substituted at a two for one ratio and a minimum of one-year clinical research experience required.

 

Licensure/Certification

• All RNs and other Clinical Research Coordinators involved in direct patient care may be required to be licensed by the medical director.
• BLS/Healthcare Provider certification required.

Experience

• One (1) year of healthcare experience required