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Fortrea

CRAs & Sr. CRAs - Radiopharmaceutical Therapies - Remote US

RemoteUnited States only
Published
Experience
Senior
Employment
Full-time
$105k–$145k/yr
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Open to US only. Set where you work from to check your eligibility.

No BS summary

Experienced CRAs with Radiopharmaceutical therapeutic expertise needed for full-service outsourcing. Requires 1+ year of independent CRO/sponsor monitoring. Must be comfortable in a fast-paced, changing, technology-based environment. Teamwork and people skills are essential.

Required skills

Clinical Monitoring

Optional skills

Radiopharmaceutical experience

Required languages

English

What you'll do

  • 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
  • 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 reports, 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

What they require

  • 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
  • Radiopharmaceutical experience is desired
  • Open to various hub locations
  • 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

  • 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)

one of the world´s largest and longest-established early-phase clinical research organizations

HealthcareEnterprisefortrea.com

What people say about this company

2.9/ 5

$105k–$145k/yr