Job description
Title: Contract Manager (For Clinical Trial sites)
Location: remote
Status: 12 month contract
Hourly rate: $50-$55
Please note: This position requires previous experience negotiating sites and vendors for clinical trials. No other backgrounds will be considered for this role.
Manage the end-to-end contract process for clinical trials and studies, including drafting, negotiating, and finalizing agreements with vendors, investigators, and other stakeholders.
Location: remote
Status: 12 month contract
Hourly rate: $50-$55
Please note: This position requires previous experience negotiating sites and vendors for clinical trials. No other backgrounds will be considered for this role.
Manage the end-to-end contract process for clinical trials and studies, including drafting, negotiating, and finalizing agreements with vendors, investigators, and other stakeholders.
- Collaborate with cross-functional teams, including clinical operations, legal, finance, and external partners, to ensure alignment on contract terms and deliverables.
- Review contract terms and conditions to identify risks, propose solutions, and ensure compliance with company policies and regulatory requirements.
- Facilitate communication and maintain strong relationships with internal and external stakeholders throughout the contract lifecycle.
- Track contract status, milestones, and deliverables to ensure timely execution and completion.
- Maintain accurate and up-to-date records of contracts and associated documentation using contract management software or tools.
- Assist in the development and implementation of standard operating procedures (SOPs) and best practices for contract management within the clinical department.
- Provide support and guidance to internal teams on contract-related matters and contribute to process improvement initiatives as needed.
- Bachelor's degree in life sciences, business administration, or related field. Advanced degree preferred.
- Minimum of 3-5 years of experience in contract management, preferably within the clinical research or pharmaceutical industry.
- Strong understanding of clinical trial regulations and guidelines (e.g., ICH-GCP, FDA regulations).
- Excellent negotiation, communication, and interpersonal skills.
- Ability to prioritize tasks, manage multiple projects simultaneously, and meet deadlines in a fast-paced environment.
- Proficiency in Microsoft Office Suite and experience with contract management software.
- Detail-oriented with a high level of accuracy and attention to detail.