Senior Site Contract Associate – Biotech

This is a fully remote position, open to applicants in Spain.

📋 Description

• Assist in executing all essential start-up contracting tasks for designated sponsors, studies, or multi-protocol initiatives.

• Create straightforward investigator grant estimates and proposal content to facilitate the proposal development process.

• Utilize and maintain contracting templates, budgets, and systems, along with tools, processes, and training materials.

• Ensure effective collaboration with sponsors, stakeholders, and RSU regions and countries.

• Offer specialized operational and financial contracting support.

• Aid in the development and/or review of core scientific, technical, and administrative documents.

• Contribute to the gathering, interpretation, analysis, and distribution of precise contracting intelligence.

• Guarantee overall contracting efficiency while adhering to project timelines and financial objectives.

• Comply with contract management and quality standards.

• Provide administrative and operational assistance to investigator site contract analysts, managers, and directors.

• Ensure the accurate completion and upkeep of internal systems, databases, tracking tools, timelines, and project plans.

⛳️ Requirements

• Bachelor’s Degree in life sciences or healthcare.

• Over 6 years of relevant experience.

• Experience in clinical site contracting within sponsor or clinical research organizations.

• Excellent negotiation and communication skills.

• Strong interpersonal abilities and a proven team player.

• Exceptional technical writing skills.

• Understanding of the regulated clinical trial landscape and knowledge of the drug development process.

• Familiarity with and capability to apply GCP/ICH and relevant regulatory guidelines.

• Awareness of applicable regulatory requirements, SOPs, and the company’s Corporate Standards.

• Strong organizational and planning skills.

• Proficient in Microsoft Office and email applications.

• Ability to interpret pricing models and prepare proposals, bid grids, and budgets.

• Strong understanding of clinical trial contract management.

🏝️ Benefits

• Health insurance.

• Flexible working hours.

• Professional development opportunities.