Clinical Investigator - Hybrid - Eagan, MN

SOLVENTUM•Eagan, MN

3d•$96,000 - $132,000•Hybrid

About The Position

At Solventum, the Clinical Investigator serves as Principal Investigator for non-significant risk clinical research studies, leading and overseeing work from study concept and planning through closeout. The role protects participants’ rights, safety, and wellbeing through protocol development, informed consent oversight, and adverse event evaluation and reporting. It ensures studies follow approved documentation, Good Clinical Practice (GCP), applicable regulations, ethical requirements, and organizational procedures throughout the study lifecycle. The investigator partners with cross-functional stakeholders to design, plan, and execute clinical research activities that generate high-quality data and support business and research objectives. The role provides clinical research expertise to help ensure studies are ethically sound, operationally feasible, and conducted with data integrity and participant safety as priorities. The position is hybrid eligible, with duties requiring travel to Eagan, Minnesota at least three days per week. Travel may include up to 5% domestic travel. Relocation assistance may be authorized. Candidates must be legally authorized to work in the country of employment without sponsorship for employment visa status.

Requirements

Bachelor’s degree or higher.
At least 2 years of clinical research experience, including application of Good Clinical Practice (GCP) requirements.
Nurse (RN) licensure or Physician Assistant (PA) licensure.
Legal authorization to work in the country of employment without sponsorship for employment visa status.

Nice To Haves

Ability to manage multiple clinical research studies, deliverables, timelines, and competing priorities simultaneously.
Ability to communicate study-related information verbally and in writing and collaborate with cross-functional teams.
Ability to apply GCP, ISO 14155, and other applicable clinical research regulations and standards to study activities.
Ability to identify, assess, and mitigate participant safety and study execution risks and support resolution of clinical study issues.
Experience collaborating with cross-functional research teams and stakeholders to support clinical study activities and deliverables.

Responsibilities

Serve as Principal Investigator for non-significant risk clinical research studies, providing leadership and oversight from study concept and planning through closeout.
Protect study participants’ rights, safety, and wellbeing through protocol development, informed consent oversight, and adverse event evaluation and reporting.
Ensure studies comply with approved study documentation, 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 help ensure studies are ethically sound, operationally feasible, and conducted with data integrity and participant safety as priorities.
Comply with corporate policies, procedures, and security standards while performing assigned duties.