Generics [U.K.] Ltd.
At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.
Viatris empowers people worldwide to live healthier at every stage of life.
We do so via:
Access – Providing high quality trusted medicines regardless of geography or circumstance;
Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and
Partnership – Leveraging our collective expertise to connect people to products and services.
Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment.
For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world.
The Role & What You Will Be Doing
Sr Manager of Clinical Supply Operations is responsible for investigational material activities for Phase I-IV assigned studies within Viatris Clinical Operations, including coordination of packaging, labelling, and distribution at Contract Packaging Vendors.
This individual will collaborate with medical, regulatory, and clinical experts/personnel to ensure that quality Clinical Supplies are provided according to departmental SOPs and applicable regulations. This position also interacts with both internal and external supply chain and logistics personnel in the procurement of clinical drug supplies.

Every day, we rise to the challenge to make a difference and here’s how the Senior Manager Clinical Supply Operations role will make an impact:

• Serves as core team member for clinical projects representing investigational materials and/or technical operations.
• Responsible for technical assessments, selection of contract packaging vendors to provide service for specific projects, review and approval of contracts, pack design, drug ordering, supply plan management for packaging and labelling activities conducted by clinical supply vendors and monitoring of budget.
• Participates in audits and monitoring of clinical supplies vendors.
• In conjunction with the clinical supply vendors and internal departments, coordinates QA/QP release of investigational materials to be used in global clinical trials.
• Reviews and approves IVRS specifications from investigational materials perspective.
• In conjunction with CRO and Regulatory, co-ordinates the design of clinical labels to meet protocol, FDA, EU and other country specific regulatory requirements.
• Writes or reviews the Study Medication Sections of the protocol and IND as required.
• In conjunction with clinical supply vendors, monitors Investigational Materials inventories and expiry/retest dates supplies.
• Trains investigators and CROs on protocol procedures related to Investigational materials.
• Creates, reviews, and revises Clinical Supply related SOPs as appropriate.
• Perform other duties as assigned.

About Your Skills & Experience

For this role, we’re looking for a candidate who has an effective combination of the following qualifications, skills and experiences:

• Clinical Supplies knowledge with comprehensive operational experience in R&D Clinical Supplies and related areas on a global level. Must possess advanced knowledge of project management, packaging, labelling and distribution of clinical studies. Knowledge of and excellent understanding of Good Manufacturing Practice (GMP) and other associated regulations, guidelines, and industry standards for clinical trials.
• Excellent interpersonal and communication skills
• Strong planning, organizational, and problem-solving skills
• B.S. Degree or related scientific discipline + 7 years pharmaceutical industry experience.
• Thorough understanding of the development and clinical supplies process
• Ability to maintain accurate records and files in accordance with GMPs, SOPs, and other regulatory requirements.
• Experience with e-mail, Windows, word-processing, database, spreadsheet applications as well as Microsoft Project and PowerPoint
• Strong decision-making, detail-oriented, multi-tasking, and negotiation skills
• Ability to work effectively in a multifunctional team environment.
• Be flexible.

At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles.
Benefits at Viatris

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Some of our benefits include the following on top of a competitive salary:

• Top Employer Accreditation, demonstrating that we provide excellent people policies and practices
• Competitive compensation package inclusive of annual discretionary bonus
• Focus on career progression with growth and development opportunities
• Hybrid work model
• Emphasis on Health & Wellness programmes
• 100% paid medical insurance and Employee Assistance Programme
• Life cover
• Excellent employer-matched pension scheme with Viatris contributing up to 11%
• 2 paid volunteer days per year

Diversity & Inclusion at Viatris
At Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of our business can be one of our greatest strengths in redefining healthcare not as it is, but as it should be. If you would like to know more about what diversity, equity and inclusion means to us, please visit
https://www.viatris.com/en/Careers/Diversity-and-Inclusion
Sustainability at Viatris
Corporate social responsibility is fundamental to the Viatris mission. We work to advance responsible and sustainable operations and leverage our collective expertise to empower people to live healthier at every stage of life, recognizing that our actions affect the stakeholders and communities we serve. To learn more about our efforts, please visit
https://www.viatris.com/en/about-us/corporate-responsibility
At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.
Viatris is an Equal Opportunity Employer.

LI-Remot

Every day, we rise to the challenge to make a difference and here’s how the Senior Manager Clinical Supply Operations role will make an impact:

• Serves as core team member for clinical projects representing investigational materials and/or technical operations.
• Responsible for technical assessments, selection of contract packaging vendors to provide service for specific projects, review and approval of contracts, pack design, drug ordering, supply plan management for packaging and labelling activities conducted by clinical supply vendors and monitoring of budget.
• Participates in audits and monitoring of clinical supplies vendors.
• In conjunction with the clinical supply vendors and internal departments, coordinates QA/QP release of investigational materials to be used in global clinical trials.
• Reviews and approves IVRS specifications from investigational materials perspective.
• In conjunction with CRO and Regulatory, co-ordinates the design of clinical labels to meet protocol, FDA, EU and other country specific regulatory requirements.
• Writes or reviews the Study Medication Sections of the protocol and IND as required.
• In conjunction with clinical supply vendors, monitors Investigational Materials inventories and expiry/retest dates supplies.
• Trains investigators and CROs on protocol procedures related to Investigational materials.
• Creates, reviews, and revises Clinical Supply related SOPs as appropriate.
• Perform other duties as assigned

For this role, we’re looking for a candidate who has an effective combination of the following qualifications, skills and experiences:

• Clinical Supplies knowledge with comprehensive operational experience in R&D Clinical Supplies and related areas on a global level. Must possess advanced knowledge of project management, packaging, labelling and distribution of clinical studies. Knowledge of and excellent understanding of Good Manufacturing Practice (GMP) and other associated regulations, guidelines, and industry standards for clinical trials.
• Excellent interpersonal and communication skills
• Strong planning, organizational, and problem-solving skills
• B.S. Degree or related scientific discipline + 7 years pharmaceutical industry experience.
• Thorough understanding of the development and clinical supplies process
• Ability to maintain accurate records and files in accordance with GMPs, SOPs, and other regulatory requirements.
• Experience with e-mail, Windows, word-processing, database, spreadsheet applications as well as Microsoft Project and PowerPoint
• Strong decision-making, detail-oriented, multi-tasking, and negotiation skills
• Ability to work effectively in a multifunctional team environment.
• Be flexible