Investigator Contracts Lead - FSP Homebased Germany

Parexel; Berlin; Vor Ort; EUR 60.000 - 100.000; Vollzeit

Zusammenfassung

An innovative biopharmaceutical company is seeking an Investigator Contracts Lead to manage site-facing contract negotiations and oversee contracting professionals. This role is pivotal in ensuring smooth operations in clinical development, where your expertise will directly impact patient wellbeing. With a focus on collaboration and innovation, you'll navigate the complexities of clinical trial agreements while enjoying exceptional professional rewards and a balanced work/life environment. Join a team dedicated to making a difference in global health and drive meaningful change in patient care.

Leistungen

Exceptional financial rewards

Training and development

Healthy work/life balance

Qualifikationen

• 5+ years in clinical development operations with a master's degree.
• 2+ years in clinical trial outsourcing with a Juris Doctorate.

Aufgaben

• Manage contract and budget negotiations with clinical investigator sites.
• Oversee contracting professionals on assigned studies.

Kenntnisse

Epidemiology

Public Health

Bioinformatics

Research Experience

Writing Skills

Ausbildung

Master's Degree in Clinical Development

Juris Doctorate or equivalent

Jobbeschreibung

When our values align theres 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 a deep conviction in what we do.

Each of us, regardless of our role at Parexel, contributes to the development of therapies that ultimately benefit patients. We take our work personally, do it with empathy, and are committed to making a difference.

Parexel FSP is currently hiring for an Investigator Contracts Lead.

Location: Homebased in Germany.

We are a single sponsor dedicated to a worldwide biopharmaceutical company that relentlessly seeks breakthroughs to improve patients' lives. Our daily innovation contributes to a healthier global community. This is a space where today's visionaries, solution seekers, and trailblazers converge to shape tomorrow's groundbreaking solutions. Together, we have the power to revolutionize patient wellbeing. Every decision and step we take is guided by our unwavering focus on patients, fostering an environment where innovation thrives.

Responsibilities:

• Manage direct site-facing contract and budget negotiations with clinical investigator sites, including initial agreements and amendments.
• Oversee other contracting professionals on assigned studies.
• Manage the Per-Subject Cost (PSC) process, including escalation and resolution of budget and non-legal term issues.
• Collaborate with other lines to plan site contracting timelines through startup.

Required experience:

• Experience with clinical study budgets and contracting negotiation principles, practices, processes, and activities.
• Knowledge of principles, concepts, and theories in an applicable business discipline.
• Experience in drafting and negotiating Clinical Trial Agreements with clinical trial sites in a global operation (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).

What we offer:

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

Apply today!

Key Skills:

Epidemiology, Public Health, Bank Secrecy Act, Bioinformatics, Fraud, Genetics, Interviewing, Law Enforcement, Qualitative Research Interviewing, Research Experience, Next Generation Sequencing, Writing Skills