Associate Clinical Trial Manager - PhD / Post-Doc Experience - Dallas, TX
Behavioral Health Market Context
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Benefits
Dallas Campus OverviewFlexible work environmentCompetitive PTO packages, starting at 20+ daysCompetitive compensation and benefits packageCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesCommunity involvement with nonprofit organizationsStructured career paths with opportunities for professional growthDiscounts on local sports games, fitness gyms and attractionsModern, ecofriendly campus with an on-site fitness centerFree on-site parkingOutdoor seating and workspace9 more items(s)
Qualifications
- •Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management
- •Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM)
- •PhD in Life Sciences;
- •Fluency in English with solid presentation skills;
- •Ability to work in a fast-paced dynamic industry within an international team;
- •Prior experience within the CRO or pharmaceutical industry not required but will be advantageous; and
- •Excellent computer (word-processing, databases, Excel, Windows), organisational, and communication skills
- •Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
- •5 more items(s)
Responsibilities
- •The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical Trial Managers in performance of project management activities
- •This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics
- •Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager;
- •Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy;
- •Compile and maintain project-specific status reports within the clinical trial management system;
- •Interact with the internal project team, Sponsor, study sites, and third-party vendors;
- •Provide oversight and quality control of our internal regulatory filing system;
- •Provide oversight and management of study supplies;
- •Create and maintain project timelines; and
- •Coordinate project meetings and produce quality minutes
- •7 more items(s)
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