Senior Clinical Project Manager - Remote USA (Solventum)

Solventum in; Maplewood (MN); Remote; USD 137,000 - 168,000; Full time

Job summary

A leading company in healthcare seeks a Senior Clinical Project Manager to lead multi-site clinical trials. The role involves managing clinical research associates and ensuring compliance with regulations. Candidates should have extensive experience in clinical research and project management. This remote position offers competitive compensation and benefits, emphasizing the importance of innovation and collaboration in healthcare.

Benefits

Medical, Dental & Vision

Health Savings Accounts

Qualifications

• At least 5 years of clinical research experience.
• 3 years managing large, multi-site clinical trials.

Responsibilities

• Lead and manage multi-site clinical trial research activities.
• Negotiate contracts with study sites and oversee performance.

Skills

Leadership

Communication

Project Management

Education

Bachelor's degree

High School Diploma/GED

Master's degree

Tools

Good Clinical Practice (GCP)

Clinical research certification (SoCRA or ACRP)

Project Management Professional Certification (PMP)

Job description

Senior Clinical Project Manager - Remote USA (Solventum) (Finance)

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:

1. 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.
2. 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.
3. Negotiating contracts with study sites and establishing clear performance expectations and key milestone activities related to site payments.
4. 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.
5. Communicating study results through presentations at technical meetings 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

• 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 (e.g., 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 trials.
• Experience working with cross-functional teams.
• Demonstrated ability to prioritize and manage multiple projects; good communication skills; customer-service orientation; and adaptability to changing work priorities and procedures.

Work location:

Remote in USA

Travel:

May include up to 25% domestic/international

Relocation Assistance:

Not authorized

Legal Work Authorization:

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.

Compensation:

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, etc.). Additional information is available at: https://www.solventum.com/en-us/home/our-company/careers/#Total-Rewards

Responsibilities include ensuring compliance with corporate policies, procedures, and security standards while performing duties.

Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. Applicants must remain vigilant against fraudulent job postings and schemes.

All email communications from Solventum regarding job opportunities will be from an email with the domain @solventum.com. Be cautious of unsolicited emails from other domains.

Note: Solventum does not expect candidates to perform work in unincorporated areas of Los Angeles County.

Solventum is an equal opportunity employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status.

Application Submission: Your application may not be considered if you do not provide your education and work history, either by uploading a resume or entering the information directly.

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