Clinical Research Associate I

NMDP•Minneapolis, MN

1d•$70,000 - $85,000•Hybrid

About The Position

This position supports the CIBMTR CRO Services team by supporting the management of one or more multi-center clinical research studies. This position performs site monitoring visits to complete source document verification and assess site compliance. Additionally, this position is responsible for coordinating and providing support for all aspects of the study including protocol and site management.

Requirements

Knowledge of clinical research study processes, study design, and protocol management.
Knowledge of medical terminology and anatomy/physiology.
Knowledge of computer proficiency, including the use of standard software (word processing, databases, e-mail) and the use of internet.
Knowledge of training and conflict resolution skills.
Knowledge of time management skills and problem-solving abilities.
Demonstrate excellent oral and written communication.
Ability to manage multiple deadlines and priorities while ensuring quality and timeliness.
Ability to perform tasks requiring excellent attention to detail.
Ability to demonstrate independent problem-solving and decision-making for straightforward situations, but requires guidance for complex situations.
Ability to analyze trends, identify issues, and escalate as appropriate.
Ability to adapt to change.
Ability to navigate processes and people involved in clinical research, demonstrating organizational awareness and interpersonal skills necessary to complete work efficiently.
Ability to travel 25-50%, both domestic and international, depending on assigned studies. Travel at times may increase up to 70% as required.
Must exemplify our NMDP values in a highly professional manner in all settings.
Bachelor’s degree in healthcare/science related field; however, upon evaluation, equivalent related experience and/or education may be substituted for the scientific or health-related degree requirement.
Minimum two years’ experience of conducting clinical research studies according to ICH GCP guidelines and/or verifying clinical data from medical records.

Nice To Haves

Knowledge of cellular therapies, diseases treated by cellular therapies, disease assessments, and common treatment complications.
Direct experience working at research sites on clinical studies, with or without direct interaction with patients.
ACRP or SOCRA certification.

Responsibilities

Perform full-scope remote and on-site monitoring visits involving source document verification, review of essential regulatory documents, and assessing site performance.
Ensure compliance with clinical trial protocols based on regulations, ICH GCP guidelines, and NMDP standard operations procedures.
Identify and communicate site findings with site study personnel and the study team.
Perform query management activities and generate study and site status reports.
With oversight and guidance, analyze trends in identified issues and author visit reports and letters. Ensures documentation and resolution of identified issues and implementation of corrective and preventative action.
Oversee and manage operational aspects of clinical trial sites in conjunction with project teams.
Assists with site activation and ensures study start-up and enrollment goals are met.
Collect and review essential documents for investigational sites, including maintenance of electronic Trial Master File.
Serves as primary liaison for site management issues for assigned studies, escalating to the clinical project manager as required.
Utilizes effective and proactive communication, relationship building, and issue management to develop and maintain good working relationships with Investigators and site staff.
Provide support to Investigators, Study Coordinators, and other appropriate site personnel regarding study workflow, overcoming obstacles and general questions regarding study conduct.
Assists in reviewing study site data and data reports to ensure timely and accurate submission and compliance with the study protocol.
Performs all duties in compliance with standard operating procedures, regulations outlined in the Code of Federal Regulations (CFR), ICH GCP guidelines, Federal Drug Administration (FDA) guidance and other applicable Federal, state, and local laws.
Assist in user acceptance testing (UAT) of clinical database management system for individual clinical trials.
Performs study tracking (e.g., CTMS, start-up, milestone, closeout); generates, reviews, and distributes management reports from internal tracking systems at requested intervals.
Develops, maintains, and presents, in conjunction with senior staff, clinical trial and project specific training materials.
Assists study related problem-solving activities internally and at trial sites.
Assists in protocol maintenance, tracking, and communications.
Works with internal and external team members to deliver high quality trial execution.
Participates in shared team responsibilities, ensuring optimal coverage of trials.
Participates in NMDP, CIBMTR, or CIBMTR CRO Services project teams as needed.
Complete and maintain all training requirements.
Develop, maintain, and continuously improve study and site management processes, guidelines, tools, templates, best practices, and overall implementation.
Other duties as assigned.