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Associate Clinical Project Manager

Apply Now Job ID R-347430 Date posted 09/06/2019

Job Description Summary

The successful Clinical Associate Project Manager (APM) will assist in the planning and execution of clinical studies in support of corporate objectives. In addition to assisting department leadership on the oversight of applicable studies, the APM is also still responsible for conducting the day-to day site management operations associated with the execution of clinical trials (including being assigned as a monitor at study sites, on as needed basis).

Job Description

  • Assist in the planning and execution of clinical studies ensuring that deliverables are completed on time and within budget;
  • Assist in the development and management of study related documents and materials such as investigational plans, case report forms, study manuals, monitoring plan, informed consents, websites, recruitment materials and other study related tools;
  • Assist in the development and submission of clinical reports and clinical study data;
  • Participate in site qualification and initiation activities, including training of investigators and coordinators;
  • Coordinate and conduct monitoring visits at investigative sites to ensure compliance to investigational plans, regulations, and timely receipt of data, including source document verification, device accountability, and writing of monitoring visit reports;
  • Oversee and review work product produced by project team members to ensure quality and compliance;
  • Management of investigative sites to ensure sponsor support of trial activities and oversight of site compliance;
  • Verify appropriate reporting and documentation of adverse events and protocol deviations per investigational plan requirements;
  • Manage internal and external vendors to ensure that deliverables are complete on time, within budget and are consistent with the scope of work;
  • Assist in planning, preparing, and presenting materials for investigator and coordinator meetings;
  • Demonstrate understanding of Business Unit’s general business functions, products, and procedures and serve on multi-disciplinary project teams as a clinical subject matter expert;
  • Participate in or run regular project team meetings;
  • Provide other project management support as assigned under the direction of project/program leadership;
  • Conduct day to day site management operations associated with the execution of clinical trials as needed;
  • Assist project/program management by providing input to sections of clinical reports for regulatory submissions, abstracts, manuscripts, and instructions for use.

Primary Work Location

USA AZ - Tempe BPV Building 3

Additional Locations

USA MN - New Hope

Work Shift

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Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

All applicants should complete the on-line application process. BD is committed to working with and providing reasonable accommodations to individuals with disabilities. If you require assistance or an accommodation because of a disability to participate in the application process, please call 855-BD-HELPS (855-234-3577) or email