Want to see how your resume matches up to this job?
        A free trial of our JobsAI will help! With over 2,000 biopharma executives loving it, we think you will too!
        Try it now — JobsAI.
      
      Role Summary
 Sr CRA 1 or Sr. CRA 2, FSP - Oncology - East Coast. Experienced Oncology Sr. CRAs residing on the East Coast to join our FSP team.
 
 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 monitoring 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, e.g., 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
 
 
 
 Qualifications
 
 - University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)
 
 - 3+ years of onsite Clinical Monitoring experience
 
 - Oncology experience
 
 - Open to major hub locations in the Northeast US
 
 
 
 Skills
 
 - Ability to work in a fast-paced environment with strict adherence to the study protocol and timelines
 
 - Adaptability to changing priorities and strong teamwork and communication skills
 
 - Technology proficiency with data collection in an electronic environment
 
 
 
 Education
 
 - See Qualifications for degree/certification requirements
 
 
 
 Additional Requirements
 
 - Frequent travel to client/site locations with occasional domestic and international travel
 
 - Physical ability to sit for extended periods, perform repetitive motions, and lift up to 15-20 lbs as needed