Clinical Study Project Manager - Oncology
Remote - any location in the continental USA or Canada
Why settle for one thing when you can have everything?
Covance gives you the best two-for-one opportunity for career growth. Who doesn't want twice the perks? Working at Covance-one of the largest FSP CROs-and partnering with one sponsor with a dedicated therapeutic focus. You can have it all!
As a Covance employee 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, Covance has an FSP opportunity to match your area of expertise.
You will enjoy the best of both worlds-all the benefits that come along with Covance's 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.
Covance's 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.
Covance's 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 assist the SM Study Lead and study team with the operational conduct of clinical studies (e.g., CTT minutes, clinical supplies planning/tracking, lab specimen tracking, imaging data reconciliation, status update reports, study closeout activities); may support a single study or multiple studies; may lead a study with limited scope (e.g., Survival Follow-up); nay be responsible for tracking study timelines and will be proficient in project management tools; may interact with internal and external stakeholders (study sites, vendors, committees, etc.) in support of clinical study objectives.
Pharmaceutical and clinical drug development experience is preferred.
TA-specific experience in Oncology is beneficial
Excellent Excel and PP skills required
Excellent written and oral communication skills