Labcorp FSP - Sr Clin Res Assoc I - MA/RI/NH in Boston, Massachusetts
Senior Clinical Research Associate I
Massachusetts, Rhode Island or New Hampshire
Why settle for one thing when you can have everything. Labcorp Drug Development gives you the best two for one opportunity for career growth. Who doesn’t want twice the perks – working at one of the largest FSP CROs—and partnering with one sponsor with a dedicated therapeutic focus.
Dedicated to an FSP project you will bring your specialized discipline to a core team working directly with one sponsor. Whether your specialization is in clinical monitoring, clinical project management, data management, biometrics or pharmacovigilance we have an FSP opportunity to match your area of expertise.
You will enjoy the best of both worlds—all the benefits that come along with our Energizing Purpose, Exceptional People and Extraordinary Potential combined with working exclusively with one sponsor using their systems and processes. This also comes with the benefit of bringing your strong therapeutic experience to a single protocol or sponsor portfolio. This allows your expertise to shine through as you also become engrained in the sponsor culture helping to bring more therapies out to patients.
Our FSP model is flexible and scalable. Our teams are collaborative and proactive – a great place for you to continue honing your therapeutic skills and growing and excelling in new exciting research.
Our reach is global – extending to 60+ countries making us one of the largest FSP CROs. So not matter where you are locating on the globe we have an FSP opportunity for you.
Essential Job Duties:
Responsible for all aspects of study site monitoring and management 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
Organize and make presentations at Investigator Meetings
Participate in the development of protocols and Case Report Forms as assigned
Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor as assigned
Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned
Independently perform CRF review; query generation and resolution against established data review guidelines on Covance or client data management systems as assigned by management
#LI - Remote
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)
In lieu of the above education requirement, candidates with a minimum of 6 years recent clinical monitoring experience will be considered.
Thorough knowledge of regulatory requirements
Thorough understanding of the drug development process
Fluent in local office language and in English, both written and verbal
Or an equivalent combination of education and experience to successfully perform the key responsibilities of the job
COVID-19 vaccination required
- Thorough knowledge of company SOPs regarding site monitoring
Two (2) years of Clinical Monitoring experience
Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
Advanced site monitoring skills
Advanced study site management skills
Advanced registry administration skills
Ability to work with minimal supervision
Good planning and organization skills
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
Works efficiently and effectively in a matrix environment
Valid Driver's License
One (1) or more year's additional experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred
Local project coordination and/or project management experience
Starting pay is $43.27 hourly (90K annually) and commensurate with experience. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including:
• Life, STD/LTD
• Paid time off (PTO) or Flexible time off (FTO)
• Company bonus where applicable
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