Conducts clinical trials as a principal or sub-investigator, ensuring participant safety, protocol compliance, and data integrity.
Locations (2)
Richfield, Minnesota, United States
Minneapolis, Minnesota, United States
Compensation
The salary range estimated for this position based in Minnesota is $240,000.00–$315,000.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy.
Responsibilities
Conduct clinical trials according to ICH GCP and local regulations
Ensure participant safety and protocol compliance
Collaborate with site leadership and cross-functional teams
Support participant recruitment and retention
Oversee investigational medical product and multiple studies
Requirements
MD or DO degree (or equivalent medical degree)
Active, unrestricted medical license in good standing
The Clinical Research Coordinator, Level 2 (CRC2) is a specialized, independent research professional who ensures oversight and compliance of both system-wide and local SHC clinical research activities.
Compensation
The pay range for this position is $32.40 - $48.60/hour.
Responsibilities
Maintains a contemporary knowledge of clinical research regulatory requirements
Tracks all aspects of projects including study, investigator and IRB information, patient recruitment activity, and financial management
Coordinates the collection, statistical analysis and dissemination of data results throughout a clinical study
Contributes in compiling, critically analyzing and preparing study results to share with research team
Demonstrates knowledge of ethical standards set forth by the Belmont Report, the Nuremberg Code and the International Conference of Harmonization GCP standards
Requirements
Bachelor's degree in Clinical Research, science or other health-care related field
Nice to have: Bachelor's or Master's in Clinical Research
Nice to have: CCRP or CCRC certification
Nice to have: coordination of intergroup or multi-site clinical studies
Lead clinical development for late‑stage oncology programs, ensuring scientific oversight, data integrity, and regulatory compliance.
Compensation
The annual base salary for this position ranges from $176,600.00 to $294,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program.
Responsibilities
Provide clinical development expertise for assigned studies
Partner with clinical, medical, and operational colleagues to implement trials
Oversee scientific oversight and data quality
Represent study team in governance meetings
Author protocols, consent documents, and regulatory submissions
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