What are the responsibilities and job description for the CRA 1 Trainees - Daytona Beach, FL ; Dallas, TX ; Madison, WI & Mid-West US - CPS - Phase I position at Fortrea?
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
Benefits
Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
Applications will be accepted on an ongoing basis.
Learn more about our EEO & Accommodations request here.
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
- 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
- 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.
Benefits
Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
- Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
- 401(K)
- Paid time off (PTO) – Flex Plan
- Employee recognition awards
- Multiple ERG’s (employee resource groups)
- Target Pay Range (based on title): $85-90K
Applications will be accepted on an ongoing basis.
Learn more about our EEO & Accommodations request here.
Salary : $85,000 - $90,000
