Clinical Investigator - Hybrid - Eagan, MN

Clinical Investigator (Solventum)

The Impact You’ll Make in this Role

As a Clinical Investigator 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:

• Serve as Principal Investigator for non-significant risk clinical research studies, providing overall leadership and oversight from study concept and planning through study closeout
• Protect the rights, safety, and wellbeing of study participants through protocol development, informed consent oversight, and adverse event evaluation and reporting
• Ensure studies are conducted in compliance with approved study documentation, Good Clinical Practice (GCP), applicable regulations, ethical requirements, and organizational procedures throughout the study lifecycle.
• Partner with cross-functional stakeholders to design, plan, and execute clinical research activities that generate high-quality data and support business and research objectives.
• Provide clinical research expertise to ensure studies are ethically sound, operationally feasible, and executed with data integrity and participant safety as top priorities.

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 AND 2 years of clinical research experience, including application of Good Clinical Practice (GCP) requirements.

AND

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

• Nurse Licensure (RN) or Physician Assistant (PA) Licensure

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

• Manages multiple clinical research studies, deliverables, timelines, and competing priorities simultaneously.
• Communicates study-related information through written and verbal formats and collaborates with cross-functional teams.
• Applies Good Clinical Practice (GCP), ISO 14155, and other applicable clinical research regulations and standards to study activities.
• Identifies, assesses, and mitigates participant safety and study execution risks and supports resolution of clinical study issues.
• Collaborates with cross-functional research teams and stakeholders to support clinical study activities and deliverables.

Work location: Hybrid Eligible (Job Duties allow for some remote work but require travel to Eagan, MN for at least 3 days per week)

Travel: May include up to 5% domestic

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).

Applicable to US Applicants Only:The expected compensation range for this position is $96,000 - $132,000, 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.