Senior Clinical Project Manager - Remote USA (Solventum)

Thank you for your interest in working for our Company. Recruiting the right talent is crucial to our goals. On April 1, 2024, 3M Healthcare underwent a corporate spin-off leading to the creation of a new company named Solventum. We are still in the process of updating our Careers Page and applicant documents, which currently have 3M branding. Please bear with us. In the interim, our Privacy Policy here: https://www.solventum.com/en-us/home/legal/website-privacy-statement/applicant-privacy/ continues to apply to any personal information you submit, and the 3M-branded positions listed on our Careers Page are for Solventum positions. As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Job Description:

Senior Clinical Project Manager, Remote USA(Solventum)

3M Health Care is now Solventum

At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue.

We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you.

The Impact You’ll Make in this Role
 

As a Senior 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 management of and carrying out of multi-site clinical trial research, including site feasibility and selection, site start-up and preparation, and review of essential tools and documents.
• Managing clinical trial sites, including monitoring and/or overseeing assigned clinical research associates in accordance with the monitoring plan, protocols, GCP, ICH guidelines, and federal regulations.
• Negotiating contracts with study sites and establishing clear performance expectations and key milestone activities related to site payments.
• Supporting: Product Development Lab personnel with clinical study and verification testing; Regulatory Affair colleagues in completion of regulatory 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 publications.

Your Skills and Expertise 

To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications:

• Bachelor’s degree or higher (completed and verified prior to start) from an accredited institution AND at least FIVE (5) years of recent and relevant clinical research experience (trial design, protocol preparation/approval, execution; including, site management/monitoring) in a private, public, government or military environment.

OR

• High School Diploma/GED from AND at least Nine (9) years of recent and relevant clinical research experience (trial design, protocol preparation/approval, execution; including, site management/monitoring) in a private, public, government or military environment.

AND

In addition to the above requirements, the following are also required:

• Three years (3) of recent experience managing large, multi-site, medical-device-related clinical trials.

Additional qualifications that could help you succeed even further in this role include:

• Master's degree in health-related field from an accredited University.
• Previous experience working in a Medical Device company is preferred.
• Experience working in a clinical hospital setting is preferred (i.e RN, MA or NP)
• Clinical research certification (SoCRA or ACRP)
• Project Management Professional Certification (PMP)
• Knowledge of Good Clinical Practice (GCP) guidelines and regulations.
• Experience writing and editing study reports, manuscripts, and collaborating with investigators in publishing study results in peer-reviewed journals.
• Previous experience executing