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Job Description
- Req#: JR139324
Employer Industry: Clinical Research Organization
Why consider this job opportunity:
- Competitive salary with additional benefits focused on well-being and work-life balance
- Various annual leave entitlements to ensure personal time off
- Comprehensive health insurance options catered to you and your family's needs
- Access to a Global Employee Assistance Programme for 24-hour support
- Flexible benefits including childcare vouchers, gym memberships, and health assessments
- Commitment to diversity and inclusion in the workplace
What to Expect (Job Responsibilities):
- Coordinate, prepare, and execute clinical study contracts in collaboration with various project stakeholders
- Support country Study Start Up strategy to meet timelines and deliverables
- Track and oversee contract status, including dispatch and return of contracts
- Negotiate financial and legal conditions while escalating issues as needed
- Serve as the single point of contact for local Legal and Ethics Review Committees (ERC)
What is Required (Qualifications):
- Bachelor's degree in business administration, law, or a related field; advanced degree or legal qualification preferred
- Minimum of 5 years of experience in contracts management, preferably in the pharmaceutical, biotechnology, or clinical research industry
- Strong knowledge of contract law and regulatory requirements relevant to clinical trials
- Excellent negotiation and communication skills to influence stakeholders
- Detail-oriented with strong analytical and problem-solving abilities
How to Stand Out (Preferred Qualifications):
- Advanced degree or legal qualification in a relevant field
- Experience with international contracts and regulations
- Proven ability to work in a fast-paced environment managing multiple priorities
- Familiarity with GCP/ICH guidelines and regulatory compliance
#ClinicalResearch #ContractsManagement #HealthcareCareers #DiversityAndInclusion #NegotiationSkills
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