Ensure the protection of study patients by verifying that informed consent procedures and protocol
Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review.
Monitor data for missing or implausible data.
Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Fortrea travel policy.
Ensure audit readiness at the site level.
Prepare accurate and timely trip reports.
Manage small projects under the direction of a Project Manager/Director as assigned.
Review progress of projects and initiate appropriate actions to achieve target objectives.
Organize and make presentations at Investigator Meetings.
Undertake feasibility work when requested.
Conduct, report, and follow-up on Quality Control (QC) visits when requested.
Negotiate study budgets with potential investigators and assist the Fortrea legal department with statements of agreements as assigned.
Track and follow-up on 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.
Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned 29) Perform other duties as assigned by management.
The statements below are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills, and duties.
Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study.
Requirements
Qualifications (Minimum Required): University or college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology.
In lieu of the above education requirement, candidates with a minimum of 3 years relevant clinical research
experience in pharmaceutical or CRO industries will be considered. Thorough knowledge of regulatory
requirements including a basic understanding of regulatory requirements in other countries.
Thorough understanding of the drug development process.
Fortrea may consider relevant and equivalent
experience in lieu of educational requirements.
Experience with CAR-T (CGT - Cell and gene therapy) Availability to travel to US Valid VISA Have a full understanding of Serious Adverse Event (SAE) reporting, process production on reports, narratives and follow up of SAEs.
Advanced study site management skills.
Advanced registry administration skills.
Ability to work with minimal supervision.
Good computer skills with good working knowledge of a range of computer packages.
Advanced verbal and written communication skills.
Ability to train and supervise junior staff.
Ability to resolve project-related problems and prioritizes workload for self and team.
Ability to work within a project team.
experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred.
Experience
Experience (Minimum Required): Three (3) years of Clinical Monitoring experience.
Additional details
Job Overview: The Senior CRA I is responsible for site monitoring and site management.
Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines.
The Senior CRA I assure the implementation of project plans, as assigned.
Function as leader for projects of limited scope, as assigned.
Assume line management responsibilities, as assigned.
Act in the project role of a Local Project Coordinator or Lead CRA as assigned. Summary of
Responsible for all aspects of study site monitoring including routine monitoring and closeout 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.
requirements are adhered to according to the applicable regulatory requirements.
Travel, including air travel, may be required and is an essential function of the job.