Investigator Contracts Lead II - Spain - FSP

When our values align, there's no limit to what we can achieve.

At Parexel , we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel , contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

At Parexel FSP , people make a difference. We have a key mission: to prevent and treat disease by bringing important new medicines and therapies to patients in need. We achieve this important goal through the expertise, experience, innovation, and commitment of our employees around the world.

Our employees have the opportunity to do meaningful things around the world, while we support them locally in environments of challenge, collaboration, flexibility and industry-leading growth potential.

Parexel FSP is looking for an Investigator Contracts Lead II in Spain , 100% remote.

In this position, you will be responsible for direct site facing contract and budget negotiations through contract execution with assigned clinical investigator sites including initial agreements and amendments and oversight of other contracting professionals on assigned studies. This also includes managing the Per-Subject Cost (PSC) process for assigned studies, managing escalation and resolution for budget and non-legal term issues from other ICL or preferred Contract Research Organizations (pCRO) and collaborating with other lines to plan site contracting timelines though start up.

Expect exciting professional challenges, but with a healthy work-life balance. Your wellbeing is as important to us as our patients.

For each role, we look for professionals who have the determination and courage to always put the patient's wellbeing first. For us, this is a job with heart.
Some details of the role:
- Contracting deliverables

- May act as single point of contact for studies with high priority or complex or unique contracting structures and strategies and is expected to be able to plan and solve for these situations with minimum oversight.

- Exercise independent judgement and decision making in areas of site contracting with moderate supervision.

- Effective management of contract and budget escalations from Functional Service Provider (FSP) / pCRO ICL with limited consultation.

- Make appropriate decisions, with limited oversight while balancing the risks for the client in making budget and contractual choices against the impacts to client clinical trial timelines

- Problem solving for site contracting issues of moderate complexity. This includes suggesting and implementing unique solutions, as needed, to achieve study goals.

- Follow client processes to develop, negotiate, track and execute global clinical study agreements with institutions and investigators participating in sponsored clinical trials.

- Work with partners to develop and oversee the global site budget process.

- Work with clinical trial sites and directly negotiate cost, business and contractual terms and conditions with investigators/institutions, making changes to contract templates within the Legal division approved parameters.

- Lead other ICL, pCRO and FSP negotiators in achieving study goals with moderate support from site contracting team leads.

- Act as primary study point of contract for site contracting issues and timelines on assigned studies.

- Partner with Legal and other divisions to manage escalations in the site budgeting and contracting space.

- Partner with Legal, Finance, pCRO and other divisions to identify and implement areas of improvement in the site contracting space.

- Applies acquired job skills and procedures to complete substantive assignments, projects and tasks of moderate scope and complexity in ap