Offer summary

Qualifications:

University or college degree or certification in a related allied health profession (e.g., nursing licensure)., 5+ years of clinical monitoring experience., Strong teamwork and people skills are essential., Ability to work in a fast-paced, technology-based environment..

Key responsabilities:

Responsible for all aspects of study site monitoring and management.

Ensure compliance with informed consent procedures and protocol requirements.

Monitor data integrity and manage registry as prescribed in project plans.

Assist with training new employees and coordinate clinical projects as a Local Project Coordinator.

Job description

We are currently seeking Experienced Sr. CRAs with 5+ years of monitoring experience, to lead and support our FSP team! We are open to experienced CRAs in Florida or the South East US.

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)
5+ years of Clinical Monitoring experience
Open to major hub locations in the South East US

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: