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Contract Negotiator
1 tydzień temu
Site Contract Analyst II - Bulgaria
ICON plc is a renowned global healthcare intelligence and clinical research organization.
We're proud to foster an inclusive environment driving innovation and excellence, and we welcome talented professionals to join us on our mission to shape the future of clinical development.
As a Site Contract Analyst II at ICON, you will be working within a large-scale, fast-paced environment, supporting the Study Start Up Team Lead in developing and executing the plan for country and site distribution. Your expertise and dedication will be essential in efficiently conducting SSU (Study Start Up) activities in the assigned countries, ensuring the smooth initiation and progress of clinical trials.
Key Responsibilities:
- Drive study initiation by reviewing and negotiating clinical site investigator contracts and budgets.
- Maintain effective communication with investigative sites, sponsors, and internal personnel regarding contract status and related documents.
- Analyse contracts, agreements, and legal documents related to clinical trial activities and vendor relationships.
- Negotiate contract terms and conditions with clients, vendors, and other stakeholders to ensure compliance with regulatory requirements and company policies.
- Collaborate with cross-functional teams to assess contract risks, identify opportunities for improvement, and develop strategies to mitigate potential issues.
- Maintain accurate records of contract status, milestones, and deliverables using contract management systems.
- Provide guidance and support to internal teams on contract-related matters, including interpretation, compliance, and dispute resolution.
Your Profile:
- Bachelor's degree in Business Administration, Legal Studies, or a related field; advanced degree or certification in Contract Management or a relevant discipline preferred.
- Minimum 2 years of experience in contract administration, contract management, or a related field, preferably in the pharmaceutical or clinical research industry.
- Strong understanding of contract law, legal terminology, and regulatory requirements related to clinical trials and vendor agreements.
- Excellent analytical and problem-solving skills, with the ability to evaluate complex contractual issues and propose effective solutions.
- Strong attention to detail and organizational skills, with the ability to manage multiple tasks and prioritize work effectively in a fast-paced environment.
