Clinical Research Associate II, Phase I - Texas/Mid-West
$100K/yr – $120K/yr
You'll complete your application on the employer's website.
$100K/yr – $120K/yr
You'll complete your application on the employer's website.
Job type
Salary
$100K/yr – $120K/yr
Sector
Posted
20 days ago
Fortrea is seeking a Clinical Research Associate II to support Phase I clinical trials. The role includes monitoring and managing study sites, protecting participant safety, ensuring data integrity, and coordinating clinical project activities.
Tags
Health Care
Life Science
Pharmaceutical
Artificial Intelligence (AI)
Accounting
Human Resources
Healthcare
Publishing
Biopharma
Bookkeeping and Payroll
Employment
Freelance
Responsibilities
Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -
Responsible for all aspects of site management as prescribed in the project plans
General On-Site Monitoring
Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data
Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested
Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs
Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
Assist with training of new employees, eg. co-monitoring
Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned
Perform other duties as assigned by management
Benefits
Remote work
Lifelancer is a global platform for talent hiring in Life Sciences, Pharma, Healthtech & IT.
London, England, GBR
https://lifelancer.com
Total Funding
$0.68M
2025-03-01
Pre Seed· $0.24M
2024-03-01
Pre Seed· $0.11M
2023-03-01
Pre Seed· $0.12M
Leadership Team
Jayesh Pandya
Co-Founder & CEO
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Qualifications
Clinical Research Associate with 1+ years of experience
Ideal candidates would have phase I experience and reside in Texas or Mid-West (Kansas, Missouri, Nebraska, Iowa, Colorado)
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
1+ years of Clinical Monitoring experience
Phase I experience
Teamwork and people skills are essential for the study to run smoothly
Ability to access and use a variety of computer software developed both in-house and off-the-shelf
Required skills
Represents the skills you have, click on the tags, Nursing Licensure
Experience
1+ years
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