drjobs Associate Director Clinical Alliance Management

Associate Director Clinical Alliance Management

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1 Vacancy
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Job Location drjobs

Princeton, NJ - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Kyowa Kirin is a fastgrowing global specialty pharmaceutical company that applies stateoftheart biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease. A Japanbased company our goal is to translate science into smiles by delivering therapies where no adequate treatments currently exist working from drug discovery to product development and commercialization. In North America we are headquartered in Princeton NJ with offices in California North Carolina and Mississauga Ontario.

Summary:

The Vendor Management & Vendor Budget and Contract Management team focuses on Clinical Portfolio Financial Management Vendor and Site Financial Management and Data Analytics. Clinical Alliance Management Associate Director supports the Global Head of Clinical Vendor Budget and Contract Management in the creation organization and operational structure of vendor management and governance. This role involves overseeing relationships with external vendors who provide clinical trial services (including and not limited to 3rd party vendors CROs and strategic partnerships (In and Outlicensing engagements codevelopment partnerships) ensuring compliance with contractual obligations regulatory requirements company standards and project timelines. By utilizing key deliverables from Business Operations Leads and Clinical Operations Leads such as benchmarking financial standard reports and operational escalations combined with creating deliverables such as KPIs and performance analysis the Clinical Alliance Management Associate Director drives vendor performance and efficiency. This position requires close understanding of the Business Operations Leads and strong collaboration with internal stakeholders clinical operations procurement legal and finance teams.

Essential Functions:

Vendor Management
Identify evaluate and select vendors for clinical trial services such as CROs laboratories and other specialized service providers with key stakeholder collaboration.
Negotiate contracts and service agreements with vendors ensuring alignment with project budgets and timelines.
Maintain ongoing relationships with vendors acting as the primary point of contact for issue resolution and performance management.
Conduct regular performance reviews and participate and contribute in CAPA resolutions where applicable to ensure compliance with regulatory requirements and company standards.

Support to Global Head and Sr. Management
Support the Global Head of Clinical Vendor Budget and Contract Management in developing and implementing the vendor management and governance framework. Including Vendor Level process map Risk Categorization Tool Metrics Framework Catalog Performance & Metrics Review Process Vendor Selection Scorecard and Feedback process.
Contribute to the strategic planning and of vendor management initiatives.
Provide insights and recommendations to enhance vendor governance and operational efficiency.

Project Improvement Efforts in coordination with the BOL and COL of each project
Monitor vendor performance metrics risk management and key performance indicators (KPIs) to ensure quality and efficiency.
Work with internal project teams to align vendor activities with overall project goals and timelines.
Centralize the oversight of vendor interactions to ensure timely delivery of clinical trial services and optimize vendor performance.
Address and resolve escalated discrepancies or issues that arise during clinical trials.

KPIs and Performance Analysis
Establish and monitor KPIs to assess vendor performance quality and efficiency.
Train BOL on KPIs and vendor performance day to day management)
Conduct regular performance analysis to identify trends address issues and implement corrective actions.
Provide detailed performance reports to senior management highlighting key insights and recommendations.
Monitor and report on vendorrelated expenses identifying opportunities for cost savings and efficiency improvements.
Utilize BOL Deliverables include the financial study outputs in the Vendor Management performance and governance structure.
Utilize data to evaluate vendor performance against industry standards and identify areas for improvement.
Implement best practices and standards derived from benchmarking to enhance vendor performance and efficiency.

Requirements:

Education
Bachelors degree in life sciences business administration or closely related field; advanced degree preferred.

Experience
Minimum of 10 years of progressive experience in clinical trial management including substantial responsibilities in vendor oversight. Experience working within a global organization and managing international vendors is strongly preferred.

Technical Skills
Indepth knowledge of GCP FDA regulations and other relevant regulatory requirements.
Strong negotiation contract management and project management skills.
Excellent communication and interpersonal skills with the ability to build and maintain relationships with external partners and internal stakeholders.
Proficiency in Microsoft Office Suite and clinical trial management systems and analytics tools.
Familiarity with clinical trial technologies and Analytics.

NonTechnical Skills
Ability to manage multiple projects and priorities in a fastpaced environment. Strong work ethic is required. Detail oriented and excellent follow through. Has the ability to flex and deal with ambiguity in a dynamic fastpaced high growth environment. Has a passion for personal learning and development to be able to grow with the company. Cultural sensitivity and ability to develop consensus within a multinational organization.

Working Conditions:

Requires up to 10 domestic and international travel. Occasional requires travel to vendor sites clinical trial locations and industry conferences. May involve working outside of regular business hours to accommodate global time zones and project deadlines.

KKNA and all of its employees have an obligation to act in accordance with the law and with integrity in all our operations and interactions

It is the policy of Kyowa Kirin North America Inc. to provide equal employment opportunity to all qualified persons without regard to race religion creed color pregnancy sex age national origin disability genetic trait or predisposition veteran status marital status sexual orientation or affection preference or citizenship status or any other category protected by law.

When you apply to a job on this site the personal data contained in your application will be collected and stored by Kyowa Kirin Inc. (Controller) which is located at 510 Carnegie Center Dr. Princeton NJ 08540 USA and can be contacted by emailing Controllers data protection officer can be contacted at . Your personal data will be processed for the purposes of managing Controllers recruitment related activities which include setting up and conducting interviews and tests for applicants evaluating and assessing the results thereto and as is otherwise needed in the recruitment and hiring processes. Such processing is legally permissible under Art. 61(f) of General Data Protection Regulation (EU) 2016/679 (GDPR) as necessary for the purposes of the legitimate interests pursued by the Controller which are the solicitation evaluation and selection of applicants for employment.

Your personal data will be shared with Greenhouse Software Inc. a cloud services provider located in the United States of America and engaged by Controller to help manage its recruitment and hiring process on Controllers behalf. Accordingly if you are located outside of the United States your personal data will be transferred to the United States once you submit it through this site. The transfer will be made using appropriate additional safeguards under the standard contractual clauses approved by regulators for transfers of personal data outside the European Union.

Your personal data will be retained by Controller as long as Controller determines it is necessary to evaluate your application for employment. Under the GDPR if you are located in the European Union you have the right to request access to your personal data to request that your personal data be rectified or erased and to request that processing of your personal data be restricted. You also have the right to data portability and to lodge a complaint with an EU supervisory authority. If you have any questions about our use of your data you may contact us by email at .

Recruitment & Staffing Agencies

Kyowa Kirin does not accept agency resumes unless contacted directly by internal Kyowa Kirin Talent Acquisition. Please do not forward resumes to Kyowa Kirin employees or any other company location; Kyowa Kirin is not responsible for any fees related to unsolicited resumes.

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Required Experience:

Director

Employment Type

Full Time

Company Industry

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