Clinical Research Coordinator - Psychiatry

Ohio State University; United States; Vor Ort; USD 52.000 - 78.000; Vollzeit

Benefits dieser Stelle

Medical, dental and vision coverage

Paid time off

Retirement plan options

Zusammenfassung

The Ohio State University in Columbus, OH, is seeking a Clinical Research Coordinator in the Psychiatry department to implement and coordinate daily clinical research activities. You will recruit, interview and enroll participants, obtain informed consent, and ensure consent processes meet regulatory and sponsor requirements.

You will also collect and document medical histories, manage data and biological samples, prepare regulatory documents, and assist with manuscripts and publications.

Qualifikationen

• Bachelor’s Degree in Biological Sciences or related field required.
• 0 years of relevant experience required.
• 2-4 years of relevant experience preferred.

Aufgaben

• Implements, coordinates and performs daily clinical research activities per approved protocols.
• Recruits, interviews and enrolls patients; obtains informed consent and ensures regulatory compliance.
• Collects, processes and evaluates samples; coordinates care and prepares case report forms.
• Assists with data collection, extraction, coding and analysis; generates study reports and manuscripts.
• Prepares regulatory documents and ensures IRB and sponsor compliance; participates in QA reviews.
• Attends meetings and contributes to development of new research protocols; coordinates external reviews.

Kenntnisse

Clinical research

Patient recruitment

Informed consent

Data collection

Regulatory compliance

IRB knowledge

Ausbildung

Bachelor’s Degree in Biological Sciences or related field

Jobbeschreibung

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Job Title: Clinical Research Coordinator - Psychiatry Department: Medicine | Psychiatry

• 60%: Implements, coordinates and performs daily clinical research activities in accordance with approved protocols; assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls patients; obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements; educates patients and families of purpose, goals, and processes of clinical study; ensures initial and follow-up appointments are appropriately scheduled and fulfilled for participants to receive patient care services according to protocol; coordinates scheduling and follow-through of surgeries, medical procedures, & other diagnostic testing; collects and documents medical histories; participates in the collection, processing & evaluation of biological samples; administers, evaluates and calculates standardized scoring of diagnostic, psychological or behavioral testing or questionnaires – (also remove any type of test or questionnaire that is not applicable; for example, if administering and scoring behavioral questionnaires, but not diagnostic or psychological tests, then only include description about the behavioral tests); coordinates and documents care of patients; assists with monitoring patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications, & provide appropriate level of care; documents unfavorable responses and notifies research sponsors & applicable regulatory agencies; participates in evaluating patients for compliance related to protocol.
• 15%: Assists with collecting, extracting, coding, and analyzing clinical research data; compiles and enters clinical research data into study database; generates reports and reviews to ensure validity of data; assists with development of clinical research study database; assists with writing sections of manuscripts, articles and other media for publication and presentation.
• 10%: Participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements; assists with planning and development of clinical study processes.
• 10%: Prepares and submits regulatory documents to applicable governing agency related to the conduct of human subject research; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; participates in planning, organizing and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; completes case report forms.
• 5%: Attends departmental meetings; attends national professional and scientific conferences to continue professional development; completes special projects as required.
• 20%: collecting and organizing data

Minimum Required Qualifications

• Bachelor’s Degree in Biological Sciences, Health Sciences or medical field, or equivalent combination of education experience required.
• 0 years of relevant experience required.
• 2-4 years of relevant experience preferred.

Additional Information

Location: Institute of Brain, Behavior and Immunology (0878) Position Type: Regular Scheduled Hours: 40 Shift: First Shift Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.

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The university is an equal opportunity employer, including veterans and disability.

At Ohio State, you’ll find work that inspires you. We offer roles and growth opportunities in countless fields and specialties — including a job that’s right for you. Ohio State benefits give you options to take care of what matters most to you — and opportunities to make adjustments as your life and needs change, including:

• Medical, dental and vision coverage, with Ohio State paying a significant portion of the cost.
• Paid time off, including sick and vacation time and 11 holidays.
• State retirement plan or an alternative retirement plan, both with generous employer contributions.

No matter your role, you’ll be part of creating what people need now: pathways to education, research and health care. Working at Ohio State means you’re part of a team with a strong sense of community and an unwavering commitment to excellence — and, of course, incomparable Buckeye spirit. We bring out the best in people, help each other succeed and learn together. By joining Ohio State, you become part of a top-20 public university with one of America’s leading academic health centers. We’re a team of dedicated colleagues with access to boundless resources that support you.

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