Clinical Project Manager (Solventum)
Remote - Minnesota
Job Description:
Clinical Project Manager (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 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 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, 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.
- Clinical research certification by SoCRA or ACRP.
- 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.
- 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.
- Current, valid Driver’s License is desired.
Work location:
Work location: Remote
Travel: May include up to [25%][domestic/international]
Relocation Assistance: Not 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
Solventum 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.
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.
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Job Profile
Regions Countries Benefits/Perks SkillsClinical Research Clinical Trials Management Communication Compliance GCP Guidelines Healthcare New Product Development Product Development Regulatory Submissions Training
Tasks- Communicate study results
- Manage multi-site clinical trial research
- Negotiate contracts with study sites
- Oversee clinical research associates
- Support product development and regulatory affairs teams
5 years
EducationBachelor's degree GED High school diploma High school diploma/GED
RestrictionsMust be legally authorized to work in country of employment without sponsorship for employment visa status
TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9