Director, Site Contract Management

Precision Medicine Group; Lecce; Remoto; EUR 70.000 - 90.000; Tempo pieno

Descrizione del lavoro

A clinical research organization is seeking a Director, Site Contract Management. This remote position requires a minimum of 8 years of relevant experience, focusing on clinical trial agreements and site budgets. Responsibilities include leading site contracting, negotiating agreements, and ensuring compliance. Candidates must have strong organizational and leadership skills. The role offers flexibility and the chance to contribute to innovative clinical trials.

Competenze

• 8+ years of relevant experience in clinical trial agreements and site budgets.
• Experience with North American/European institutions.
• Proven skills in strategy, planning, and execution to improve quality and productivity.

Mansioni

• Lead the global site contracting function.
• Establish processes for contract management.
• Review, draft, and negotiate various agreements.
• Resolve complex issues with legal and finance.
• Ensure compliance with policies and standards.

Conoscenze

Organizational skills

Communication skills

Leadership and negotiation skills

Proficiency in MS Office

Relationship-building skills

Formazione

4-year college degree in a scientific or healthcare discipline

Strumenti

Site budget tools

Descrizione del lavoro

We are seeking a Director, Site Contract Management to join our team!

This is a remote-based opportunity with flexible location options in the following countries: UK, Spain, Italy, Hungary, Poland, Romania, Serbia, or Slovakia.

At Precision for Medicine, we believe in advancing personalized medicine through innovative assays and clinical trials. Our mission is to help biotech and pharmaceutical companies accelerate the development of targeted treatments.

Position Summary

The Director will ensure the success of the site budget and contract negotiations globally. Responsibilities include drafting, reviewing, negotiating, and tracking legal agreements such as confidentiality agreements, clinical study agreements, and amendments. The role involves collaborating with Clinical Operations, legal, and finance teams to resolve contract issues and ensure alignment with study timelines. The position also involves participating in strategic initiatives like the Precision Site Network and Rapid Start-up.

Essential functions include:

1. Leading the global site contracting function.
2. Establishing processes and procedures for contract management.
3. Reviewing, drafting, and negotiating various agreements.
4. Resolving complex issues with legal, finance, or senior management.
5. Ensuring compliance with policies and standards.
6. Updating study teams on contract status.
7. Overseeing agreement execution across portfolios.
8. Managing contract metrics and database maintenance.
9. Identifying process improvements and implementing policies.
10. Representing the organization in meetings as a Subject Matter Expert.
11. Performing other tasks as assigned.

Qualifications

Minimum Required:

• 4-year college degree or equivalent, preferably in a scientific or healthcare discipline.

Other Required:

• 8+ years of relevant experience in clinical trial agreements and site budgets.
• Experience with North American/European institutions.
• Proven skills in strategy, planning, and execution to improve quality and productivity.

Preferred:

• Experience in contract research, biotech, or pharmaceutical industries.

Skills and Competencies:

• Strong organizational and communication skills.
• Ability to multitask and prioritize.
• High self-motivation and independence.
• Leadership and negotiation skills.
• Professionalism and good interpersonal skills.
• Sound business judgment and proactive work style.
• Proficiency in MS Office and site budget tools.
• Discretion handling sensitive issues.
• Ability to work independently and in a virtual team environment.
• Relationship-building skills.
• Willingness to travel domestically and internationally, including overnight stays.

Please apply in English.

We comply with privacy policies and are an Equal Opportunity Employer. We do not make employment decisions based on protected characteristics. If you need accommodations during the application process, contact us.

Beware of fraudulent job offers; our organization will only extend offers through verified communication channels.