Clinical Investigator - Hybrid - Eagan, MN

Solventum•Eagan, MN

2d•Hybrid

About The Position

Solventum is seeking a Clinical Investigator to serve as Principal Investigator for non-significant risk clinical research studies. The role provides leadership and oversight from study concept and planning through closeout, while protecting study participants’ rights, safety, and wellbeing. The investigator develops protocols, oversees informed consent, and evaluates and reports adverse events. The Clinical Investigator ensures studies follow approved documentation, Good Clinical Practice (GCP), applicable regulations, ethical requirements, and organizational procedures throughout the study lifecycle. The role partners with cross-functional stakeholders to design, plan, and execute clinical research that generates high-quality data and supports business and research objectives. The investigator provides expertise to ensure studies are ethically sound, operationally feasible, and conducted with data integrity and participant safety as priorities. This is a hybrid role requiring travel to Eagan, Minnesota, at least three days per week. Domestic travel may be up to 5%. Relocation assistance may be authorized. Applicants 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.
Legally authorized to work in the country of employment without sponsorship for employment visa status.

Nice To Haves

Experience managing multiple clinical research studies, deliverables, timelines, and competing priorities simultaneously.
Ability to communicate study-related information in writing and verbally 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, leading and overseeing studies from concept and planning through closeout.
Protect 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 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.