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
Lead efforts to build and maintain strong relationships with clinical trial sites, ensuring effective communication and collaboration throughout the study lifecycle.
Lead and manage local quality and compliance activities for drug and non-drug projects, ensuring readiness for inspections and adherence to GCP and regulatory standards.
Responsibilities
Lead design and implementation of local quality management activities
Conduct site visits and in-house quality checks
Provide quality metrics and dashboards to local management
Advise DevOps staff on procedural frameworks and guidelines
Clinical Team Manager / Sr. (CTM) - HemOncThermo Fisher Scientific · Remote, US