FSP Sr. Clinical Research Associate - Florida

Davita Inc.; Daytona Beach (FL); Hybrid; USD 125,000 - 140,000; Full time

Job summary

A leading healthcare company is seeking Experienced Senior Clinical Research Associates to join their FSP team in Florida or the Southeast US. This role requires a strong background in clinical monitoring, ensuring compliance with research standards while working in a dynamic environment that emphasizes teamwork and adaptability. Employees receive comprehensive benefits including medical, dental, and a competitive 401(K) plan, alongside a target salary range of $125,000 to $140,000 annually.

Benefits

Medical, Dental, Vision, Life Insurance

401(K)

Paid time off (PTO) - Flex Plan

Employee recognition awards

Multiple ERGs (employee resource groups)

Qualifications

• Minimum 5 years of clinical monitoring experience required.
• Comfortable in a fast-paced, technology-based environment.
• Experience with team collaboration and adapting to changing priorities.

Responsibilities

• Responsible for comprehensive monitoring of clinical trial sites.
• Ensure adherence to protocols and data integrity.
• Assist in training new employees and manage clinical projects.

Skills

Clinical Monitoring

Teamwork

Adaptability

Tech Savvy

Education

University or college degree or certification in allied health

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, ifapplicable) 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:

• 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): $125-140K

#LI - Remote

Applications will be accepted on an ongoing basis.

Learn more about our EEO & Accommodations request here.