COVANCE By Labcorp
Published
June 17, 2021
Location
Telecommute
Category
Job Type
Work Setting
Remote / Home-based, In-office

Description

Job Overview:

Clinical Scientist - Vaccines
Remote in the USA or Canada

**Must have medical monitoring experience

***Position leads Phase 1-3 Clinical Trials and oversees medical monitoring.  This is not a laboratory/research scientist role.

Why settle for one thing when you can have everything?

Covance by Labcorp 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

Starting pay is up to $67.31 and commensurate with experience. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including:
• Medical
• Dental
• Vision
• Life, STD/LTD
• 401(K)
• ESPP
• Paid time off (PTO) or Flexible time off (FTO)
• Company bonus where applicable

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