Job ID R-442874 Date posted 06/20/2022 Apply

Clinical Project Specialist (Remote)

Job Description Summary

Job Description

Be part of something bigger!

BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

Job Description:

BD Diagnostic Systems is seeking a Clinical Project Specialist for our Medical Affairs department located in San Diego, CA.  The Clinical Project Specialist is accountable for the achievement of key functional business objectives, and oversight of key activities in a platform or program area.  Responsibilities include representing Medical Affairs (MA)/Clinical Operations on Core Teams/Product Development Teams for existing and/or new product initiatives.  The Clinical Project Specialist demonstrates understanding of advanced technical/scientific principles applicable to the platform/program area of focus and those of associated disciplines (such as R&D, Quality, Business, or Project Management).

The Clinical Project Specialist represents the interest of the patient and the health care worker and has basic understanding of unmet medical/clinical needs,  provides input into product design on behalf of MA, and contributes to ongoing evaluations of product safety. The Clinical Project Specialist applies moderate knowledge of clinical trial design and conduct of moderately complex studies when interacting with the extended clinical operations team, and is responsible for writing the Medical Affairs Strategy Document as well as the Clinical Trial Plan. The Clinical Project Specialist has working knowledge of local regulations and BD policies and procedures and moderate knowledge of BD products, product development process, ISO standards and elements of design control.

Responsibilities also include generating clinical evidence plans including publication strategies.  The Clinical Project Specialist will help coordinate and lead the team through journal publications and scientific conference presentations and represent Medical Affairs in market development activities.

Additional responsibilities may also include reviewing and providing input to product labeling and Health Risk Assessments.  The Clinical Project Specialist may contact external KOLs regarding trends in clinical practice and potential impact of product issues. The Clinical Project Specialist possesses critical thinking and analytical skills and is capable of evaluating research by processing complex data to arrive at conclusions.

The Clinical Project Specialist provides MA oversight and expertise to study teams, extended functional teams or work groups, inspires effective business/function dynamics, and imparts a sense of commitment to business/function goals.


  • Demonstrates advanced level of technical/scientific discipline applicable to role, and advanced working level understanding of technical aspects of disciplines of key associated disciplines, such as R&D, Quality, Business, Project Management.

  • Creates coherent, professional documentation and correspondence of moderate complexity. Is able to draw conclusions from primary and other written and/or verbal sources, present, and / or act on them effectively.  Is effective when speaking among peers, team members and functional or Business Management.  Work product may require limited review by managers from technical or stylistic point of view.

  • Develops and prepares training materials consistent with role with technical and stylistic input from more senior associates.  Creates and delivers moderately complex presentations to primarily internal audiences; is able to respond to questions extemporaneously.

  • Recognizes potential problems and takes preventive steps.  Recommends solutions for more complicated or ambiguous issues for consideration.  May lead an ad-hoc team to resolve issues.

  • Identifies possible process improvement opportunities in own area of responsibility and works to implement them. May participate in CI initiative in own or related area of responsibility.

  • Manages multiple complex or multi-stage projects. Is able to mentor/teach others about Project Management principles, tools & processes.   Is proficient in the use of formal tools (e.g. MS Project) and creation and/or customization of templates.

  • Manages most activities without supervision.  Interactions with manager involve periodic updates on activities, discussion of issues, proposals for resolution.

  • Asserts own ideas and persuades others.  Fosters collaboration among team members.  Is recognized as leader within function or business unit.

  • Contributes to short term planning and decisions for groups and/or projects.

  • Estimates resources required and works with Manager to ensure availability of required supplies and/or resources for individual and/or group activities.  Has some impact on quality, cost, and/or productivity.  May be asked to provide supporting data for a formal budget process.

  • Carries out tasks and activities that are defined by Manager and in local business/operating plans.

  • Willingness to travel approximately 10% (domestic and international)


  • Bachelor degree required, with preferred education/experience focus in Molecular Biology, Clinical Microbiology, the life sciences, clinical, laboratory or other relevant technical areas.  Professional certification (clinical research, laboratory) preferred.

  • Education and experience sufficient to independently contribute on multi-functional project teams as a subject matter expert in platform area of focus, or on functional teams across businesses/regions.  

  • Experience with IVD clinical trials, in particular Point of Care and/or Molecular diagnostics a plus.

  • Minimum 1 year experience in Medical Affairs, or as a functional Core Team member, or as a clinical project manager.

For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

Why join us?

A career at BD means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our associates can fulfill their life’s purpose through the work that they do every day.

You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program — which includes competitive pay, benefits, continuous learning, recognition, career growth, and life balance components — is designed to support the varying needs of our diverse and global associates.

To learn more about BD visit

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.



Primary Work Location

USA CA - San Diego (IDS)

Additional Locations

Work Shift


Working in

San Diego (IDS)

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Working in

San Diego (IDS)

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"Purpose driven company where associates work every day to make healthcare better. A lot of great initiatives going on to make BD the best MedTech company in the world."
Anonymous, Franklin Lakes, NJ

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