What are the responsibilities and job description for the Clinical Project Manager position at 3M?
Job Description:
Clinical Project Manager/Research Associate
Collaborate with Innovative 3Mers Around the World
Choosing where to start and grow your career has a major impact on your professional and personal life, so it’s equally important you know that the company that you choose to work at, and its leaders, will support and guide you. With a diversity of people, global locations, technologies and products, 3M is a place where you can collaborate with other curious, creative 3Mers.
This position provides an opportunity to transition from other private, public, government or military experience to a 3M career.
The Impact You’ll Make in this Role
Within the Medical Division, you’ll independently assume Clinical Research responsibilities related to developing and executing plans for internal and external clinical studies for marketed products, product modifications, or for new products in collaboration with product teams, regulatory, and sales and marketing personnel.
Within the Medical Division, you’ll independently assume Clinical Research responsibilities related to developing and executing plans for internal and external clinical studies for marketed products, product modifications, or for new products in collaboration with product teams, regulatory, and sales and marketing personnel.
As a Clinical Project Manager you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:
- Leading the activities involved in the development of and carrying out of clinical trial research.
- Implementing global standard operating procedures to ensure good clinical practice and regulatory compliance in all work-related activities.
- Supporting: Product Development Lab personnel with clinical study and verification testing; Regulatory Affair colleagues in completion of submissions; and product development teams by collecting clinical trial evidence for both new product development and for evidence for maintaining marketed products.
- Communicating study results through presentations at technical meeting and may publish in refereed journals.
- Developing a knowledge and understanding of assigned products, customers, customer needs in areas of responsibility.
Your Skills and Expertise
To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications:
To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications:
- Bachelor’s degree or higher (completed and verified prior to start) from an accredited institution
- Two (2) combined years of clinical research, biomedical, and/or medical device industry experience (claims substantiation, ensuring integrity of clinical study documentation file, trial design, protocol preparation/approval, execution).
- Two (2) combined years of experience working with Good Clinical Practice (GCP) guidelines, FDA guidelines, International Standards Organization (ISO), and/or International Conference on Harmonisation (ICH) .
Additional qualifications that could help you succeed even further in this role include:
- Master's degree in health-related field from an accredited University.
- Clinical research certification by SoCRA or ACRP.
- Experience writing and editing study reports, manuscripts, and collaborating with investigators in publishing study results in peer-reviewed journals.
- Having experience working with cross-functional teams.
- Demonstrated ability to prioritize and manage multiple projects; of good communication skills; being customer-service orientated; and having the ability to adapt to change in work priorities and procedures.
Work location: Hybrid Eligible Job Duties allow for some remote work but require travel to Maplewood, MN Site at least 1 day per week
Location Name: Maplewood, MN
Travel: May include up to 15% domestic/international
Relocation Assistance: May be authorized
Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).
Supporting Your Well-being
3M offers many programs to help you live your best life – both physically and financially. To ensure competitive pay and benefits, 3M regularly benchmarks with other companies that are comparable in size and scope.
Chat with Max
For assistance with searching through our current job openings or for more information about all things 3M, visit Max, our virtual recruiting
Learn more about 3M’s creative solutions to the world’s problems at www.3M.com or on Twitter @3M.
Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.
Our approach to flexibility is called Work Your Way, which puts employees first and drives well-being in ways that enable 3M’s business and performance goals. You have flexibility in where and when work gets done. It all depends on where and when you can do your best work.
Pay & Benefits Overview: https://www.3m.com/3M/en_US/careers-us/working-at-3m/benefits/
3M is an equal opportunity employer. 3M will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status.
Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.
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