Clinical Scientist, FSP – Support
This is a role that involves supporting medical monitoring. This is not a laboratory scientist role.
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 CRO and partnering with one sponsor with a dedicated therapeutic focus. You can have it all!
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 and this also comes with the benefit of bringing your strong therapeutic experience to allow your expertise to shine through.
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 and exciting research.
Our reach is global – extending to 60+ countries making us one of the largest FSP CROs. No matter where you are located on the globe, we have an FSP opportunity for you.
In this role, the selected candidate will assist the Clinical Scientist Protocol Lead and study team with the clinical/scientific conduct of clinical studies e.g., adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management; may support a single study or multiple studies; may lead a study with limited scope (e.g., Survival Follow-up); and may interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives
EBS/BA/MS/Ph.D. in Life Sciences with 2+ yrs relevant clinical research experience
COVID-19 vaccination required
Pharmaceutical and clinical drug development experience in a Clinical Scientist role
2 Years of Medical Monitoring experience required
Proven ability to effectively manage multiple complex studies
Excellent Excel and PP skills required
Excellent written and oral communication skills
TA-specific experience preferred
Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including:
Paid time off (PTO)
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
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