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 SolventumAt 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 RoleAs 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.ORHigh 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.ANDIn 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 IDE trialsHaving experience working with cross-functional teams.Demonstrated ability to prioritize and manage multiple projects; good communication skills; being customer-service orientated; and having the ability to adapt to change in work priorities and procedures.Work location: Work location: Remote in USATravel: May include up to 25% domestic/internationalRelocation Assistance: Not authorizedMust be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).Supporting Your Well-beingSolventum offers many programs to help you live your best life – both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope.Applicable to US Applicants Only:The expected compensation range for this position is $137,439 - $167,981, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: https://www.solventum.com/en-us/home/our-company/careers/#Total-RewardsResponsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. Applicants must remain alert to fraudulent job postings and recruitment schemes that falsely claim to represent Solventum and seek to exploit job seekers.Please note that all email communications from Solventum regarding job opportunities with the company will be from an email with a domain of @solventum.com. Be wary of unsolicited emails or messages regarding Solventum job opportunities from emails with other email domains.Please note, Solventum does not expect candidates in this position to perform work in the unincorporated areas of Los Angeles County.Solventum is an equal opportunity employer. Solventum 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.Solventum Global Terms of Use and Privacy StatementCarefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at Solventum are conditioned on your acceptance and compliance with these terms.Please access the linked document by clicking here, select the country where you are applying for employment, and review. Before submitting your application you will be asked to confirm your agreement with theterms.