Manager, R&D Procurement

Employment as a Contingent Worker aligns well with individuals seeking career flexibility and non-traditional work arrangements, while also being motivated to produce exceptional results in prominent roles. Magnit Direct Source is a service provided by Magnit Global that connects top-tier talent directly to an industry-leading company. Daiichi Sankyo, Inc. and Magnit Global, in collaboration, offer flexible contingent assignments across diverse projects creating opportunities for engaging work.  As a Contingent Worker, you will not be employed Daiichi Sankyo, Inc. You will be employed by our Managed Service Provider, Magnit Global, which oversees the majority of our temporary contract recruitment.
 

Manager, R&D Procurement (Level II or Level III) - based on years of experience. 
Preference to local candidate to be based in NJ and come onsite 1-4 times a week as needed (average is onsite 2 days a week).

The purpose of this job is to work with DS teams to assess, select, negotiate and execute clinical trial vendor contracts.  Performs financial reconciliation and negotiation of Vendor contracts prior to study termination and contract closure.  Manages all aspects of sourcing and negotiating Vendor contracts to ensure that the contracts are cost effective.  Provides oversight of Vendor contracts, change orders and works with the Vendor for resolution of all issues/ discrepancies.  

Expertise in complex outsourcing models supporting Clinical R&D and PhI to PhIV outsourced services (e.g., CRO, core labs, Biomarker, central labs); Must have strong problem-solving skills and is able to work in complex categories.  Follow all processes, procedures and/or systems to improve organizational efficiencies and cost controls.

Procurement - Manages all Outsourcing activities from vendor assessment, RFP, selection, contract budget, payment schedule & scope negotiation through to contract execution.  Supports internal customers to help ensure that vendors meet required service level.

Demonstrates expanded understanding of procurement principles, legal language, vendor selection criteria. May assist with the development of a sourcing strategy by spending category that reduces costs, reduces timelines and improves quality. Develops detailed bid analysis for the R&D functional group’s review. May be involved in other ad hoc special projects as they arise.

Communication - Leads contracts related communication with vendors. Respond to questions from internal staff regarding status of contracts. Interacts with vendors on standard administrative matters and contract terms. Appropriately escalates issues and conflicts. This position will work cross-functionally to execute the outsourcing process.

Contract Execution- Builds content of the contract, verifies the unitized budget against the needs, conducts rigorous negotiation of business terms with validation of rates from service providers. Making sure the payment schedules are cash neutral and in-line with deliverable timelines. Responsible for the negotiation, preparation, and execution of  contracts on a timely basis. Management and oversight of clinical development contracting process, review and approval in accordance with company polici

Negotiations - Advanced negotiation skills to drive cost savings. Thinking and acting strategically to drive continuous improvement.

Ensure optimal partnerships with internal stakeholders and outside vendors to deliver commitments with a high level of value, quality and performance.

Interpersonal skills - Manage and maintain collaborative relationships within R&D, Legal, Quality and Finance, as well as with external parties.  Ability to eliminate barriers to resolve procurement and contract issues in a timely manner.

Experience:
Minimum 5 years in clinical trial outsourcing, health sciences or related field (clinical trials). Daiichi Sankyo US is globalizing and interfacing with other departments/functional areas based in Japan.
Advanced WORD and Excel skills - i.e. ability to modify/re-format documents in MS Word; create a final contract in MS Word; in MS excel - write formulas in excel and analyze data.
Must have good organizational skills; able to prioritize workload and tasks; excellent time management skills. 
Must be able to work independnetly and make sound decisions.
Candidate will need to maintain and use a tracker to keep status of the tasks/contract requests.
Must have experience with any of the PhI – PhIV clinical trial vendor contracts.
Experience with laboratory service agreements will be highly preferred. This individual will be working closely with the DS bio-analysis groups (part of translation medicine) and clinical pharmacology group.
Experience with CRO contracts is preferred/acceptable.
Must having outsourcing experience from pharma/bio-tech industry.
Bachelors Degree (in Life Sciences preferred)

Hourly Pay Rate Range (dependent on location, experience, expectation) The pay range that Magnit reasonably expects to pay for this position is: $45 - $61/hr
Benefits: Medical, Dental, Vision, 401K (provided minimum eligibility hours are met)
 

All qualified applicants will not be discriminated against and will receive consideration for employment without regard to protected veteran status, disability, race, color, religion, sex, age, sexual orientation, gender identity or national origin.

 

QUALIFICATION/LICENSURE
Work Authorization : US Citizen
Preferred years of experience : 5 years
Travel required : No travel required
Shift timings : Onsite, then Hybrid possible