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Job Requirements of Clinical Contract Administrator III:
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Employment Type:
Contractor
-
Location:
Arden Hills, MN (Onsite)
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Clinical Contract Administrator III
Careers Integrated Resources Inc
Arden Hills, MN (Onsite)
Contractor
Job Title: Clinical Contract Administrator III
Location: Hybrid Arden Hills, MN 55112
Work Schedule: 3 days onsite / 2 days remote
Hours: 30 40 hours per week
Contract Type: 3-month W2 contract with high potential for extension based on performance and business needs
Pay Range: $50 to $ 57.29
Must-Have Skills
Position Overview
This position, based in the Legal department, supports global clinical studies through the preparation, review, and negotiation of a high volume of clinical study agreements and related documents. The Clinical Contract Administrator III will collaborate with global internal teams and external vendors to streamline and manage the contracting process.
Key Responsibilities
Required Qualifications
Preferred Qualifications
Location: Hybrid Arden Hills, MN 55112
Work Schedule: 3 days onsite / 2 days remote
Hours: 30 40 hours per week
Contract Type: 3-month W2 contract with high potential for extension based on performance and business needs
Pay Range: $50 to $ 57.29
Must-Have Skills
- In-depth understanding of clinical contracting terms and conditions (non-negotiable)
- Ability to read, interpret, redline, and negotiate contract terms with a practical, business-focused approach
- Advanced proficiency in Microsoft Office (Word, Excel, PowerPoint) and Adobe software
- Strong written and verbal communication skills
Position Overview
This position, based in the Legal department, supports global clinical studies through the preparation, review, and negotiation of a high volume of clinical study agreements and related documents. The Clinical Contract Administrator III will collaborate with global internal teams and external vendors to streamline and manage the contracting process.
Key Responsibilities
- Prepare clinical study agreements and related documents (e.g., hospital use agreements, device purchase agreements) using approved templates
- Independently review and revise contract language proposed by clinical sites in accordance with company policies and procedures
- Escalate contract issues appropriately and coordinate resolution with Legal, Risk Management, and clinical teams
- Manage a high-volume workload efficiently in a fast-paced environment
- Interface with internal teams including Clinical, Global Clinical Operations, and Contract Research Organizations
- Monitor group inboxes, triage requests, and assign contract reviews
- Schedule and support Global Regulatory Legal team meetings, including minute-taking
- Maintain tracking spreadsheets for active clinical studies
- Ensure accurate execution and proper upload of contracts to the contract management system
- Organize and manage digital folders and contract repositories
- Identify and propose process improvements to enhance contracting efficiency
Required Qualifications
- Bachelor s degree with 5+ years of relevant professional experience; OR
- High School Diploma / GED or Associate degree with 7+ years of related experience (preferably within a legal department of a medical device or pharmaceutical company)
- Demonstrated expertise in clinical contracting processes and terminology
- Strong ability to negotiate and manage contracts with a solution-oriented mindset
- High proficiency in Microsoft Word, Excel, PowerPoint, and Adobe
Preferred Qualifications
- Experience in the medical device industry (strongly preferred)
- Proven ability to manage multiple priorities and meet deadlines without sacrificing accuracy
- Experience collaborating with global stakeholders across legal and clinical teams
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