Offer summary

Qualifications:

5+ years of experience in clinical development operations or clinical trial outsourcing with a master's degree., 2+ years of experience in clinical development operations or clinical trial outsourcing with a Juris Doctorate or equivalent., Experience with clinical study budgets and contracting negotiation principles., Knowledge of applicable business discipline principles and concepts..

Key responsabilities:

Lead direct site-facing contract and budget negotiations with clinical investigator sites.

Manage the Per-Subject Cost (PSC) process for assigned studies.

Oversee other contracting professionals on assigned studies and resolve budget issues.

Collaborate with other teams to plan site contracting timelines through start-up.

Job description

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.

Parexel FSP is currently hiring for an Investigator Contracts Lead.

Home-based in Turkey.

Single sponsor dedicated to a worldwide biopharmaceutical company that relentlessly seeks breakthroughs to improve patients’ lives. Their daily innovation contributes to a healthier global community. This is the space where today’s visionaries, solution-seekers, and trailblazers converge to shape tomorrow’s groundbreaking solutions. Together, we have the power to revolutionize patients’ well-being. Every choice we make and every step we take is guided by our unwavering focus on patients, fostering an environment where innovation thrives.

Investigator Contracts Lead (ICL ) is 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 through start-up.

Required experience:

Experience with clinical study budgets and contracting negotiation principles, practices, processes, and activities.
Knowledge of the principles, concepts, and theories in applicable business discipline
Experience in drafting and negotiation of Clinical Trial Agreements with clinical trial sites in a global operation is preferred.

Education

5+ years of experience in clinical development operations or clinical trial outsourcing with a master’s degree.
2+ years of experience in clinical development operations or clinical trial outsourcing with a Juris Doctorate (or equivalent).

We offer exceptional financial rewards, training, and development. Expect exciting professional challenges but with a healthy work/life balance. We value your welfare just as highly as that of our patients.

Apply today!

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