Sub-Investigator
Lake City, FL, US
Scientific
Masters Degree
Part Time, Direct Hire
40.00 - 60.00 hour
Experienced (Non-Manager)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
Lake City, FL, US
40.00 - 60.00 hour
Experienced (Non-Manager)
Part Time, Direct Hire
Biotechnology/Pharmaceuticals
On-site
Scientific
Masters Degree
First Shift (Day)
Job details
(Sub-I)
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Location: Lake City, FL
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Job Type: Contract – 20-30 hours with potential to go full time or direct hire in the future
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Pay: 40.00 -60.00 an hour
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A Licensed Nurse Practitioner/Physician Assistant background is required
Kelly Science and Clinical is hiring a Sub-Investigator for one of our well-known site network clients. This position is a contract position that will be onsite in Lake City, FL site that is known for their strong family culture and values. This is part-time position with average hours between 20-32 hours per week. The opportunity does have a possibly to turn full-time or convert to permanent headcount in the future. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
Job Description
Under the guidance and supervision of the Principal Investigator (PI) or Medical Director, the Nurse Practitioner/Physician’s Assistant (Sub-Investigator) upholds the integrity and quality of clinical trials by ensuring all activities comply with federal, state, and local regulations, IRB approvals, and OMRC policies and procedures. This role is primarily responsible for accurately performing visit procedures and collecting patient data in accordance with study protocols, while safeguarding the health, safety, and welfare of research participants. Additionally, the NP/PA Sub-Investigator may serve as Study Coordinator for select, limited studies.
Essential Duties and Responsibilities:
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Review, comprehend, and adhere to assigned study protocol.
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Assist trial Investigators in screening and review of potential study participants’ eligibility.
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Conduct subject visits.
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Maintain case report forms, patient charts and documentation.
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Ensure that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements.
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Collect and enter data, as necessary.
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Review lab results, imaging reports, and other study-specific reports.
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Complete required protocol training
Qualifications/Requirements:
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Master’s Degree required
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Licensed Nurse Practitioner/Physician Assistant
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Trained in phlebotomy
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Infusion experience preferred
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Sound knowledge of FDA regulations, ICH-Good Clinical Practices (GCP) and ISOs
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Solid teamwork, organizational, interpersonal, attention to detail, and problem-solving skills
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Strong written and verbal communication skills
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Ability to multi-task, work under time constraints, work independently and cooperatively with interdisciplinary teams
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Strong computer skills in appropriate software and related company clinical systems is required
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