Pharmaceutical Clinical Associates, LLC
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N. Jersey,
NJ
Responsibilities will include, but are not limited to, the following:
1. Perform and manage all activities associated with the development and execution of contracts with Clinical Research Organizations performing clinical trial services and other vendors as necessary
2. Prepare study specific request for proposals (RFPs); manage and influence RFP process (vendor selection), competitive bidding negotiations, benchmarking and sourcing strategy
3. Prepare contracts, negotiate any requested changes to wording, identifying changes to the Legal department and coordinate any changes requested in areas of the contract that are critical to Celgene’s interest.
4. Track, manage and monitor all changes to study scope ensuring timely change order finalization and implementation
5. Negotiate contract and change order costs of moderate to high complexity
6. Manage vendor relationships and issue resolution of moderate to high complexity
7. Monitor vendor performance in accordance with contract, utilizing metrics and benchmarking
8. Involved in projects or programs (complex and multiple)
9. Lead Medical Operations Initiatives
10. Responsible for making decisions & direction of outcomes
11. High organizational impact
12. Contribute to strategy and new processes, Identify new best practices & Contribute to continuous improvement
13. Anticipate & prevent problems & create backup plans
14. Requires minimal supervision, independently author contractual documents and design and revise templates as required
15. Able to lead others, provide direction to teams and coach lower level staff
16. Interact with internal and external customers
17. Member of cross-functional teams- may lead mtgs. as appropriate and influence line functions
18. Update tracking system with all contracts/cost information
19. Maintain an electronic library of previously negotiated contracts
20. Train & coach others in processes and industry practices
21. Maintain business intelligence through monitoring outsourcing environment & awareness of industry trends
Skills/Knowledge Required:
· Advanced knowledge of contract terms and conditions ( T&C)
· Advanced knowledge of benchmarking, market analyses and financial negotiations
· Advanced problem solving skills in a team environment
· Excellent negotiation or influencing skills
· Proficient in drug development process
· Competent in computer skills, oral & written communication & multi-tasking
· Ability to manage personal timelines provide input to support staff timelines timelines
· Ability to establish and influence team timelines & expectations
· Knowledge of GCP guidelines
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Experience and Skills:
4+ years in the Pharmaceutical Industry; 3+ years in outsourcing Phase I –IV clinical trial services, BA/BS degree in life sciences, business, finance or equivalent (MBA/MS-4+ years in the Pharmaceutical Industry; 2+ years in outsourcing
Phase II-IV clinical trial services)
Additional Information:
Job Level: Any
Number of Openings: 1
Years of Experience: Any
Level of Education: Any
Salary: TBD
Starting Date : TBD
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Pharmaceutical Clinical Associates is always accepting employment inquiries from professionals interested in our opportunites. If you are interested in career opportunities at Pharmaceutical Clinical Associates please use our online resume formto apply. Pharmaceutical Clinical Associates is an Equal Opportunity Employer.
N. Jersey, NJ
N. Jersey, New Jersey
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