Director, Global CTM & Clinical Ancillary Management - Ancillary Services
Apply NowCompany: LabConnect
Location: Johnson City, TN 37601
Description:
Overview
LabConnect improves lives by partnering with pharmaceutical and biotech companies, and clinical research organizations (CROs) to accelerate the development of new medicines around the world.
We are an independent, global, one-stop-shop focused on delivering Central Laboratory Services that are tailor-made, timely and flexible to meet the evolving study demands of traditional to increasingly complex trials. Additionally, we provide Functional Service Provider (FSP) Solutions, supporting our clients with scientific and technical expertise, acting as an extension of their team, coordinating all laboratory related needs, advising on strategies for lab data collection and providing end-to-end analytical and logistical solutions.
Job Summary
As the Director of Clinical Trial Materials & Clinical Ancillary Supplies, you will be responsible for overseeing the production and leadership of global clinical trial operations in highly regulated environments. This role combines both strategic leadership and operational oversight, ensuring the business objectives of growth, profitability, and efficiency are met. The Director will also lead clinical ancillary supplies and management, ensuring proper inventory management, serviceable equipment, and distribution.
Essential Duties and Other Responsibilities:
Education/Experience/Skills Required:
Working Location:
Read more below and get ready for your next great employment adventure!
Some of the Perks our LabConnectors Love:
We are a growing and global team which Values People First, Quality Focused, Customer Centered, Technology Driven and Accountability Always. In addition to great perks and challenging work assignments, we invest in our people with enriching career growth opportunities.
We believe in a friendly and collaborative environment with open lines of communication. Join our team and discover how your work can impact the lives of people all over the world.
It is the policy of LabConnect to provide equal employment opportunities without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, marital status, veteran status, sexual orientation, genetic information, or any other protected characteristic under applicable law.
Equal Employment Opportunity Posters:
https://www.dol.gov/agencies/ofccp/posters
If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please email talent@labconnect.com or call +1(423)722-3155.
For more information, visit www.labconnect.com
LabConnect improves lives by partnering with pharmaceutical and biotech companies, and clinical research organizations (CROs) to accelerate the development of new medicines around the world.
We are an independent, global, one-stop-shop focused on delivering Central Laboratory Services that are tailor-made, timely and flexible to meet the evolving study demands of traditional to increasingly complex trials. Additionally, we provide Functional Service Provider (FSP) Solutions, supporting our clients with scientific and technical expertise, acting as an extension of their team, coordinating all laboratory related needs, advising on strategies for lab data collection and providing end-to-end analytical and logistical solutions.
Job Summary
As the Director of Clinical Trial Materials & Clinical Ancillary Supplies, you will be responsible for overseeing the production and leadership of global clinical trial operations in highly regulated environments. This role combines both strategic leadership and operational oversight, ensuring the business objectives of growth, profitability, and efficiency are met. The Director will also lead clinical ancillary supplies and management, ensuring proper inventory management, serviceable equipment, and distribution.
Essential Duties and Other Responsibilities:
- Operational Oversight: Direct all activities related to global kitting assembly and inventory management of clinical trial materials, ensuring compliance with FDA and other regulatory standards.
- International Coordination: Maintain a dotted-line reporting structure with international kit build operations, ensuring consistency, best practices, and operational alignment across global sites for optimal customer experience.
- Ensure operational excellence of clinical ancillary supplies and management, maintaining standard operating procedures, training, and other compliance related activities.
- Cross-Functional Collaboration: Work closely with senior leadership, finance, logistics, and other departments to align operational goals with overall business objectives.
- Continuous Improvement: Foster a culture of continuous improvement, identifying opportunities to streamline operations, reduce costs, and enhance operational efficiency.
- Other Duties as Assigned: Perform additional tasks and responsibilities as necessary to support the organization's goals.
Education/Experience/Skills Required:
- Master's degree with 4 years in a manufacturing/assembly environment or bachelor's degree with 6 years related experience preferred.
- Experience working in a federally regulated environment is required.
- Experience leading international operations, in globally regulated environments (FDA, FAA, EMA) with laboratory, logistics, inventory and/or clinical trial management experience preferred.
- European and/or the Asia Pacific experience preferred.
- Collaborative across business functions.
- Strong communication, including professional presentation skills.
- Excellent management skills.
- Ability to perform analytical and financial analysis of business KPIs.
Working Location:
- Johnson City, TN
- Hybrid - 3 days a week in office
Read more below and get ready for your next great employment adventure!
Some of the Perks our LabConnectors Love:
- Financial Security (base pay, 401k match and possible annual bonus eligibility)
- Health Benefits beginning on date of hire
- PTO plan plus 11 Paid Company Holidays and 1 day to Volunteer in your community
- Short and Long-Term Disability, Life and AD&D
- We celebrate our differences, which enrich our Culture
We are a growing and global team which Values People First, Quality Focused, Customer Centered, Technology Driven and Accountability Always. In addition to great perks and challenging work assignments, we invest in our people with enriching career growth opportunities.
We believe in a friendly and collaborative environment with open lines of communication. Join our team and discover how your work can impact the lives of people all over the world.
It is the policy of LabConnect to provide equal employment opportunities without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, marital status, veteran status, sexual orientation, genetic information, or any other protected characteristic under applicable law.
Equal Employment Opportunity Posters:
https://www.dol.gov/agencies/ofccp/posters
If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please email talent@labconnect.com or call +1(423)722-3155.
For more information, visit www.labconnect.com