Clinical Research Coordinator Position Available In Hillsborough, Florida

Job Description:

Title:

Clinical Research Coordinator Are you the right candidate for this opportunity Make sure to readthe full description below.

Location:

Brandon FL Type/Duration:

Contract, 6 months

Schedule:

Monday-Friday, core daytime business hours based onclinic hours, could have some earlier morning starts

Start Date:

ASAP Summary of Key Responsibilities:

Primary responsibility is toscreen, enroll and follow study subjects ensuring protocolcompliance and monitoring while the subjects are on study.

Responsible for all data collection, source documentation,completing study specific case report forms, and submission ofadverse experience reports.

Duties and Responsibilities:

Duties include but are not limited to:

• Supports enrolling patients onto the clinical trial throughscreening, enrollment and follow up of eligible subjects accordingto protocol requirements
• Ensures the protection of study patients by verifying informedconsent procedures and adheres to protocolrequirements/compliance
• Collects, completes, and enters data into study specific casereport forms or electronic data capture systems
• Ensures timely and accurate data completion
• Collects blood samples and tracks shipments and requestssupplies as needed
• Implements study-specific communications
• Ensures timely adherence to protocol requirements
• Responsible for completion of all required documentation
• Maintains accurate and complete records including regulatorydocuments when applicable, signed informed consent forms, sourcedocumentation, subject logs and study-related communications
• Communicates all study-related issues to appropriate studycolleagues or manager
• Apprises principal investigator and management of all studyspecific medical issues for guidance
• Attends study specific meetings as required or asked to doso
• Reviews and responds to any monitoring findings and escalatesissues
• Organizational and prioritizing capabilities
• Computer skills with demonstrated abilities using web-basedapplications, electronic data capture, and MS Word or Excel
• Professional communication
• Communicate and work effectively with a diverse team ofprofessional
• Interpersonal skills, detail-oriented and meticulous
• Work independently in a fast pace environment with minimalsupervision at off-site facilities

Ref:

#568-Clinical