What are the responsibilities and job description for the Clinical Research Spec - Exempt (22983) position at Advanced Clinical?
We are currently searching for a skilled professional to join a well-known client’s team as a contract Clinical Research Specialist in Mounds View, Minnesota. The Clinical Research Specialist role will oversee, design, and execute clinical evaluation studies supporting new products with strong medical or commercial potential. This role requires a detail-oriented professional capable of managing clinical trial activities, ensuring compliance with regulatory standards, and collaborating cross-functionally to deliver high-quality clinical outcomes. Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity.
RESPONSIBILITIES
• Design, plan, and develop clinical evaluation research studies in alignment with strategic objectives.
• Prepare and author study protocols, patient record forms, and supporting documentation.
• Conduct both registered and non-registered clinical studies to evaluate product safety, performance, and applicability.
• Interpret clinical data and study results for use in regulatory submissions, product development, and new device/drug/consumer applications.
• Oversee operational aspects of clinical trials in partnership with project teams, ensuring adherence to SOPs, Good Clinical Practice (GCP), and applicable country regulations.
• Support clinical trial budgeting processes and may oversee clinical supply logistics.
• Assist with or lead site and vendor selection activities to ensure high-quality study execution.
• Deliver assigned projects from concept to implementation while following established policies and timelines.
• Provide guidance to junior professionals or support staff as needed and contribute to team knowledge sharing.
EXPERIENCE
Minimum of 2 years of related clinical research experience
EDUCATION
Bachelor’s degree in engineering, life sciences, or related medical/scientific field
To be a best-fit your strengths must include:
• Site management experience (either at a clinical site or with a sponsor).
• Hands-on experience with CTMS, EDC, and TMF systems.
• Strong understanding and application of Good Clinical Practice (GCP).
Full-time employees are also eligible for benefits options such as health coverage, life insurance, disability insurance, and 401k benefits.
At Advanced Group, our commitment to diversity and inclusion in every part of our organization is crucial to fulfilling our mission and demonstrating our REAL values. Advanced Group is committed to providing employment opportunities without regard to sex, race, color, age, national origin, religion, gender identity or expression, sexual orientation or sexual preference, pregnancy or maternity, genetic information, marital status, disability, veteran status, or any other basis protected by applicable federal, state or local law.
Advanced Group complies with federal and state disability laws and makes reasonable accommodations for applicants and candidates with disabilities. If a reasonable accommodation is needed to participate in the job application or interview process, please contact accommodationrequest@advancedgroup.com.