Top 8 Clinical study manager Jobs in Jeffersonville, In

Clinical Research Coordinator II - New Albany, IN
Iterative Health —New Albany, IN
- Full-time
- Mid-level
- 3 years
- Bachelor's degree
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Clinical Research Coordinator I -RN
Iterative Health —New Albany, IN
- Nursing
- RN License
- Quality control
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Clinical Research Coordinator I
Ora —Louisville, KY
- Weekends as needed
- Vital signs
- Clinic experience
- Clinic
- Dental insurance
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Clinical Research Coordinator V
University of Louisville —Louisville, KY
- $48,225 - $72,389 a year
- Online Application
- Mid-level
- Bachelor's degree
- Team management
8d
Director of Outpatient Services - Addiction Recovery
Wooded Glen Recovery Center —Jeffersonville, IN
- Full-time
- CPR Certification
- Addiction Medicine
- BLS Certification
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1d
Clinical Research Nurse I
University of Louisville —Louisville, KY
- $61,147 - $91,721 a year
- Online Application
- Nursing
- Medication administration
- RN License
8d
Clinical Research Nurse II
University of Louisville —Louisville, KY
- $103,067 a year
- Online Application
- Nursing
- RN License
- Mid-level

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Clinical Research Coordinator I
Ora —Louisville, KY
Once onsite, our CRC I's will administrate various technician-based tasks by collecting, recording, and organizing subject and research information during…
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Clinical Research Nurse I
University of Louisville —Louisville, KY
This individual will coordinate the implementation of clinical research projects; organize the clinical research team; and serve as a navigator for study…
$61,147 - $91,721 a year
8d

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Clinical Screening Coordinator (Patient/Community Outreach)
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Complete database query reviews for study candidacy and conduct outbound calls for study interest. Return all phone calls/email responses to interested patients…
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Evolution Research Group —Columbus, OH
With 19 wholly owned clinical sites and 5 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies.
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Clinical Research Coordinator II - New Albany, IN

Iterative Health -
New Albany, IN

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Job Details

Full-time

Qualifications

Productivity software

Full Job Description

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.

We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.

We are seeking a full-time, experienced Clinical Research Coordinator - Level II (CRC II). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.

Responsibilities:

Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management. Manage a full schedule of complex study visits and corresponding tasks with minimal direction.
Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals
Schedule all patient research visits and procedures consistent with protocol requirements
Conduct patient visits as outlined within each study protocol
Dispense study medication, collect vital signs and perform ECGs
Perform blood draws, process and ship specimens per study protocol and IATA regulations
Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms. Maintain high quality data entry within established timelines
Act as point of contact for study participants
Adhere to Research SOPs, Good Clinical Practices, and the study protocols
Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager, central Iterative Health team, and PI throughout the study. Resolve routine sponsor and CRO issues independently
Ensure all safety data is reviewed by the PI in a timely manner
Maintain inventory of study equipment and supplies onsite at all times
Contribute to status updates to management; contribute and implement ideas to improve site performance
Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality.
Schedule and prepare for monitor visits
Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations
Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance
Complete and maintain case report forms per FDA guidelines, and review them against the patient's medical record for completeness and accuracy

Iterative Health Expectations

All employees are expected to:

Perform quality work within deadlines with or without direct supervision
Interact professionally with other employees, customers and suppliers
Work effectively as a team contributor on all assignments
Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations

Qualifications

Medical Assistant, LPN, Associates or Bachelor's degree in a clinical or scientific-related discipline preferred
Minimum 3 years of clinical research experience
IBD experience is a must
Ability to own issues and problem solve independently
Experience in phlebotomy preferred
Strong written and verbal communication skils
Ability to read, interpret, and apply clinic policies and research protocols
Ability to use standard office software
Must be able to lift up to 25 pounds

At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact [email protected].

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clinical study manager jobs in jeffersonville, in

Clinical Research Coordinator II - New Albany, IN

Clinical Research Coordinator I -RN

Clinical Research Coordinator I

Clinical Research Coordinator V

Director of Outpatient Services - Addiction Recovery

Clinical Research Nurse I

Clinical Research Nurse II

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