contribute to the operational planning and execution of one or more clinical trials
develop leadership and technical skills as part of a global, cross-functional team
apply project management, communication, and collaboration skills in support of our clinical trials
have specific operational responsibilities for a single study or across multiple studies (e.g., operational deliverables, clinical & ancillary supplies planning/tracking, lab specimen tracking, etc.)
responsible for tracking study timelines using project management tools
share technical expertise with team members
interact with internal and external stakeholders (e.g., study team, vendors, committees) in support of clinical trial objectives

Requirements

Bachelor’s degree with two (2) years or master’s degree with one (1) year of Pharmaceutical and/or clinical drug development experience
Degree in life sciences, preferred
Working knowledge of clinical research regulatory requirements (e.g., GCP and ICH)
Ability to manage multiple competing priorities with good planning, time management and prioritization skills
Good understanding of the principles of project planning & project management
Building analytical skills to drive operational milestones
Interact with key stakeholders across department, division, and company.
Problem solving, prioritization, conflict resolution, and critical thinking skills
Solid communication, writing, and presentation skills
Intermediate knowledge in Microsoft office or similar (Excel, PowerPoint, Word, Outlook, etc.)

Benefits

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

project managementclinical drug developmentregulatory requirementsGCPICHanalytical skillsoperational planningclinical trial executiontimelines trackingclinical supplies planning

Soft Skills

leadershipcommunicationcollaborationtime managementprioritizationproblem solvingconflict resolutioncritical thinkingpresentation skillsinterpersonal skills