Offer summary

Qualifications:

University or college degree or certification in a related allied health profession (e.g., nursing licensure)., 6 months of Clinical Monitoring experience or 2 years of study coordinator experience or equivalent., Phase I experience preferred., Must reside in specified locations. .

Key responsabilities:

Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites.

Ensure study staff have received proper materials and instructions for patient entry into the study.

Verify adherence to informed consent procedures and protocol requirements to protect study patients.

Complete Serious Adverse Event (SAE) reporting and assist with training of new employees.

Job description

Fortrea's Clinical Pharmacology Team is hiring CRA 1s with Phase I experience! We are seeking candidates in the below locations:

Daytona Beach, FL

Dallas, TX

Madison, WI

Mid-West - (OK, KS, MO, NE, IA, CO, WY)

WHAT YOU WILL DO

You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.

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

Requirements

University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
6 months of Clinical Monitoring experience or 2 years of study coordinator experience or equivalent
Phase I experience preferred
Must reside in locations listed above

The important thing for us is you are comfortable working in an environment that is:

Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
Changing priorities constantly asking you to prioritize and adapt on the spot.
Teamwork and people skills are essential for the study to run smoothly.
Technology based. We collect our data directly into an electronic environment.

What do you get?

Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to: