Clinical Research Coordinator I - Hemostasis Treatment Center

Clinical Research Coordinator I - Hemostasis Treatment Center jobs in United States

Tags

25+ applicants

Original Job Post

Vanderbilt University Medical Center

0+ years exp

66

FAIR MATCH

Experience Level

100

Skill

26

Industry Exp.

68

Responsibilities

With assistance, prepares and processes new IRB research proposals, amendments, continuing review applications and adverse event reports according to institutional and departmental policies and procedures and federal regulations

Prepares and maintains documents required to be maintained and available internally and for regulatory authorities and/or the sponsor prior to, during and after the conduct of a clinical/translational trial. Participates in periodic site visits from sponsor, regulatory authorities and others to review research, source documentation and research procedures

Procures equipment and supplies needed to fulfill project requirements

Records data from source documentation and/or participant interaction onto case report forms (either paper or electronic) with awareness and attention to the requirements for accuracy, completeness and timeliness. Attends to query resolution in a timely manner. Assures research information is collected and stored in a manner that is compliant with regulations/policies and good clinical practice

Performs packaging and ships study specimens (blood, urine, etc.) to the sponsor or laboratory in accordance with sponsor and shipping guidelines and regulations, maintaining appropriate documentation

With direction assists with study completion, study closeout and archiving of study files, ensuring completeness and continuity of all study data, performing ongoing checks of clinical/translational data that has been entered on the case report forms (paper or electronic) or in reports

With supervision, develops and manages study budgets, monitoring efficient invoicing and taking appropriate action to maintain clinical trial billing compliance

Serves as an advocate for human subjects by establishing and maintaining communication with Investigators, research staff, Sponsors, participants and representatives of professional organizations, participant advocates, and the public responsible for, or concerned about, protections for human participants of research and through ongoing monitoring of trial processes and participants

Participates in the determination of eligible candidates for study participation, assuring participants fulfill eligibility requirements. With guidance, assesses and evaluates potential participants pertinent medical and historical information to ensure only appropriate subjects are enrolled in clinical/translational trials and remain eligible for continued participation. Engages in open and positive communication with study participants and coworkers

With direction, performs or instructs others in performing procedures for research as they are described in the protocol, deviating from the protocol only when a subject's safety is at risk and in a timely manner reports all deviations from the protocol to the Principal Investigator and/or senior personnel who will determine if a protocol amendment or other safety reporting to appropriate funding/regulatory agencies is required

The responsibilities listed are a general overview of the position and additional duties may be assigned

Benefits

A comprehensive benefits package which may include health, disability, retirement and/or wellness offerings to enhance your well-being and professional growth.

Glassdoor

3.8

Vanderbilt University Medical Center is a nonprofit institution specializing in patient care, research, and nobility in medical education.

Nashville, Tennessee, USA

https://www.vumc.org/main/home

Late Stage

Total Funding

$35.3M

Key Investors

Arnold Ventures

National Institute on Aging

Advanced Research Projects Agency for Health

2026-07-07

Grant

2025-07-02

Grant· $25M

2024-11-15

Grant· $3.3M

Leadership Team

Jeffrey Balser

President

Recent News

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PRWeb

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Qualifications

Relevant Work Experience

Less than 1 year

Bachelor's

Required skills

Represents the skills you have, click on the tags, Study Design and Conduct, Qualitative Research Methods, Quantitative Research Methods, Project Coordination

Experience

Entry level