Senior Director Clinical Site Budget Contracts
Senior Director Clinical Site Budget Contracts
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$ 212900 - 354800
1 Vacancy
Job Description
The Senior Director is responsible for leadership of the team of Site Contracts Leads (SCLs) for the assigned therapeutic areas and the daytoday management of the vendors (e.g. CROs FSPs etc. with who we work for site budget and contract negotiationrelated areas. This individual is responsible for managing the global SB&C operational model including internal and vendor staff who are responsible for conducting site budget and contract negotiations. The Senior Director interacts with cross stakeholder senior level management external vendors collaboration partners and clinical study personnel.
In a typical day you will:
- Think strategically about Regenerons ideal approaches to conducting site contracting and drive solutions while ensuring compliance
- Manager the contracting operational model for assigned areas which includes a combination of inhouse vs. outsourced negotiations
- Partner with colleagues in the Law Department and other stakeholder groups as needed to continuously enhance the operational model and prioritize assignments across assigned therapeutic areas
- Maintain key site contracting metrics for vendors and direct reports ensure that internal systems are updated in a timely accurate and complete manner and maintain an overview of contract statuses and issues in order to proactively communicate progress risks issues or changes thatmay impact quality timelines and/or budget
- Act as a point of contact for clinical program and study level contract escalations
- Provide innovative and flexible operational solutions and options and proactively creates and implements risk mitigation strategies
- Identify and recommends changes to practices and policies including initiating and participating in strategic projects initiatives and continuous improvement projects
- Ensure inspection readiness throughout the clinical program lifecycleStaff Management
- Help drive decision making and integrates all operational considerations for studies to ensure that contract finalization goals are attainable prior to implementation Vendor Oversight
- Be accountable for the daytoday management of the applicable vendors across the portfolio in partnership with Clinical Trial Management Strategic Sourcing & Procurement Study Optimization Law Department and Vendor Management colleagues
To be considered you must possess:
- Bachelors degree
- Minimum of 15 years of direct experience with global Phase 14 clinical site agreement and budget negotiations (at a biopharmaceutical company or CRO) required including strong U.S. site negotiation experience
- Minimum of 10 years of people management and U.S. site contractingexperience required
- Minimum of 5 years of experience working with a vendor for global outsourcedclinical site contracting
- Therapeutic areaspecific experience required (e.g. oncology hematologygeneral medicine and/or immunology & inflammation)
- J.D. or MBA preferred
- People Management Experience
- Expertlevel understanding of global site budget and contract negotiations and advanced interpersonal communication skills influencing and problemsolving skills to achieve results and develops plans to meet strategic and operational targets in alignment with The Regeneron Way
- Ability to synthesize complex information and communicate it to a wide variety of audiences
- Ability to effectively spearhead ongoing process improvements (including crossstakeholder strategic initiatives)
- Ability to provide strategic direction and guidance for assigned book of work
- Analytical skills with a data driven approach to planning executing and problem solving
- Budget management experience
- Ability to build train manage and coach high performance and growth teams
- Demonstrated vendor management experience
- Extensive experience in global clinical trial operations
- Ability to travel up to 25
Does this sound like you Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits which often include (depending on location) health and wellness programs fitness centers equity awards annual bonuses and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race color religion or belief (or lack thereof) sex nationality national or ethnic origin civil status age citizenship status membership of the Traveler community sexual orientation disability genetic information familial status marital or registered civil partnership status pregnancy or parental status gender identity gender reassignment military or veteran status or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment unless the accommodation would impose undue hardship on the operation of the Companys business.
For roles in which the hired candidate will be working in the U.S. the salary ranges provided are shown in accordance with U.S. law and apply to U.S.based positions. For roles which will be based in Japan and/or Canada the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S Japan or Canada please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity right to work educational qualifications etc.
Salary Range (annually)
Required Experience:
Exec
Employment Type
Full-Time
