Investigator Contracts Lead - FSP Homebased Germany
Investigator Contracts Lead - FSP Homebased Germany
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Job Description
When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal to improve the worlds 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 were committed to making a difference.
Parexel FSP is currently hiring for an Investigator Contracts Lead.
Homebased in Germany.
Single sponsor dedicated to aworldwide biopharmaceutical companythatrelentlessly seeks breakthroughstoimprove patients lives. Their daily innovation contributes to ahealthier global community. This is the space wheretodays visionaries solutionseekers and trailblazers convergeto shapetomorrows groundbreaking solutions. Together we have the power torevolutionise patients wellbeing. Every choice and step we make is guided by our unwavering focus on patients fostering an environment whereinnovation thrives.
Investigator Contracts Lead (ICL is responsible for direct sitefacing contract and budget negotiations through contract with assigned clinical investigator sites including initial agreements and amendments and oversight of other contracting professionals on assigned studies. This also includes managing the PerSubject Cost (PSC) process for assigned studies managing escalation and resolution for budget and nonlegal term issues from other ICL or preferred Contract Research Organisations (pCRO) and collaborating 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 the principles concepts and theories in an 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 masters 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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Employment Type
Full-Time
