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Full-time

Clinical Research Associate II, Phase I - Texas/Mid-West

$100K/yr – $120K/yr

AI-powered talent hiring platform for life sciences, pharma, and ITScience & PharmaceuticalPosted 20d ago

You'll complete your application on the employer's website.

Job description

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

Interested in this role?

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