Site Contract Specialist

Join us as a Site Contract Specialist to support clinical trial contracts for pharmaceutical and biotech companies, ensuring compliance, quality, and timely site activation.

Location: Mexico

Responsibilities

• Draft, review, negotiate, and finalize agreements with study sites.
• Negotiate investigator grant budgets and contractual terms within approved parameters.
• Ensure compliance with negotiation parameters, approval authority, and contractual processes.
• Identify and escalate legal, financial, and operational risks.
• Coordinate with internal teams to align site startup activities with contractual activities.
• Achieve target cycle times for site activations.
• Follow guidelines and processes for escalation of issues.

Requirements

• Bachelor's degree or equivalent with relevant academic/vocational qualification.
• 2-5 years of relevant experience or equivalent combination of education, training, and experience.

Additional Information

• Work schedule: Standard (Mon-Fri).
• Environmental conditions: Office setting.
• Ability to work in upright/stationary position for 6-8 hours.
• Repetitive hand movements, frequent mobility, occasional crouching, bending, twisting.
• Light to moderate lifting (up to 20 lbs).
• Use of computer software, effective communication, multitasking under variable conditions.