Eclaro

Please be sure to list the city and state where the candidate currently resides in, under their name on the resume and in the comments section of Beeline.. 3+ years of experience with interacting with a wide range of suppliers (e.g., Contract Research Organizations, Cooperative groups, Clinical laboratories, Core laboratories including ECG and Imaging service providers): initiating, negotiating, and executing legal and/or financial agreements in the clinical trials environment- biotech or pharmaceutical industry.. groups, Clinical laboratories, Core laboratories including ECG and Imaging service providers): initiating,. This individual contributor role has task-level responsibility for in-house and outsourced studies while ensuring adherence to the client's outsourcing strategies within a specific therapeutic area(s) and is accountable to support clinical trial vendor partnerships across select or multiple service categories of clinical trial activities in R&D.. 401k Retirement Savings Plan administered by Merrill Lynch

outsourcing manager

JOB TITLE: Outsourcing Manager Location: Lawrenceville, NJ (100% onsite)Duration: 6 months initial (potential extension/potential right to hire) The candidate must be able to work onsite at Lawrenceville, so local candidates only please. Please be sure to list the city and state where the candidate currently resides in, under their name on the resume and in the comments section of Beeline. It must be Please note that the EM will NEED THREE RESOURCES. All suppliers will be able to submit 3 candidates initially. I can open this up if the EM needs additional resumes down the road. Must Have List: • 2-5 years contract management experience with direct negotiation experience• 3+ years of experience with Clinical Development and understanding of clinical operations• 3+ years of experience with interacting with a wide range of suppliers (e.g., Contract Research Organizations, Cooperative groups, Clinical laboratories, Core laboratories including ECG and Imaging service providers): initiating, negotiating, and executing legal and/or financial agreements in the clinical trials environment- biotech or pharmaceutical industry.• Degree in Legal, Life science, Business Administration or equivalent. Advanced degree a plus. Background Job Description: Position SummaryThis individual contributor role has task-level responsibility for in-house and outsourced studies while ensuring adherence to the client's outsourcing strategies within a specific therapeutic area(s) and is accountable to support clinical trial vendor partnerships across select or multiple service categories of clinical trial activities in R&D. Key Responsibilities• Drive outsourcing activities by interfacing with operational teams, support groups and service providers forsuccessful selection, contracting and execution of outsourced studies while ensuring compliance withregulatory standards, ethical practices, outsourcing and procurement policies and procedures• Drive the success of projects to meet short-term objectives & adhere to project schedules• Support Outsourcing team in a variety of tasks across outsourcing, alliance management, FSP operations andFinancial/ Resource accountability• Communicate with business partners and internal clients regarding contractual issues as needed• Provide operational expertise and support, guidance and training to teams on all aspects of outsourced work• Ensure alignment of teams to the related Client outsourcing strategies Qualifications & Experience• Minimum of a BA or BS Degree in Legal, Life science, Business Administration or equivalent. Advanced degree aplus.• Clinical development experience of 3 to 5 years of relevant industry experience (pharma, biotech, CRO) required.• Experience engaging with a wide range of suppliers (e.g., Contract Research Organizations, Cooperativegroups, Clinical laboratories, Core laboratories including ECG and Imaging service providers): initiating,negotiating and executing legal and/or financial agreements in the clinical trials environment- biotech orpharmaceutical industry• Proven experience in managing key internal and external stakeholders effectively by frequently soliciting inputand gathering and incorporating feedback into processes as appropriate• Effective management of cross-functional, multi-cultural teams and demonstrated ability to work and influencewithin a matrix structure• Proven time management skills and ability to be flexible to meet job demands, manage multiple priorities andtake on new initiatives and improvement efforts• Demonstrates a high level of adaptability in dealing with ambiguous and complex work environment andbalances multiple demands on role in a responsive and professional manner.• Ability to sustain high levels of performance in a constantly changing environment If you feel you are qualified with the required skills and if you are interested, please free to send your word version most updated resume TAILORED to the job description above to June@eclaro.com or call (212)804-7476. If hired, you will enjoy the following Eclaro Benefits:<ul><li>401k Retirement Savings Plan administered by Merrill Lynch</li><li>Commuter Check Pretax Commuter Benefits</li><li>Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro</li></ul> Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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