
Clinical Supply Specialist - LATAM/Europe- Remote
- Experience
- Junior
- Employment
- Full-time
- Company size
- Enterprise
Open to GB only. Set where you work from to check your eligibility.
No BS summary
Clinical Supply Specialist (LATAM/Europe) — remote/telecommute with applicant location requirement: United Kingdom. Requires a Bachelor’s Degree in Life Science or Clinical Supply Chain (or similar) and minimum 1 year clinical research plus 1 year clinical supply chain operations experience. IT literacy with skills in Excel; hands-on IRT experience preferred.
Core skills
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. Why Worldwide We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us! What does the Supply Chain Department do at Worldwide Clinical Supply Specialist will plan, implement, monitor and improve company supply strategy including collaboration with Project Management, Vendor Management, DLS Leadership, Finance and vendors. What you will do Plan, implement and monitor study supply strategy overall supply chain strategy in order to maximize efficiency and productivity Optimize supply levels to ensure continuity while minimizing carrying costs Control manufacturing and delivery processes Collaborate with Project Management, Vendor Management, and DLS Leadership Develop and maintain detailed inventories of study drug Develop procedures to increase efficiency throughout the supply chain while ensuring quality and safety; implements subsequent changes to processes. Collaborate with DLS Leadership to define and implement key supply chain KPIs at study and functional levels Identify process bottleneck and implement solutions in a timely manner Performs other related duties as assigned. What you will bring to the role Strong planning skills Logical and systematic approach to work Good time management, with the ability to work under pressure, maintain accuracy and keep to deadlines Ability to solve problems and make decisions, as well as to think strategically and laterally Excellent relationship management skills, with the ability to work collaboratively with internal and external teams Negotiation and influencing skills Business management and analytical skills IT literacy, skills in Excel and the ability to handle electronic data Understanding of risk management in the context of the supply chain Your background Bachelor’s Degree in Life Science or Clinical Supply Chain Management or a similar relevant field Clinical research setting experience required (1 year minimum) Clinical supply chain operations experience required (1 year minimum) Hands-on experience with supply chain functionality in an IRT system (preferred) Sense of ownership, critical thinking, detail-oriented, and problem-solving skills Excellent communication skills We love knowing that someone is going to have a better life because of the work we do. To view our other roles, check out our careers page at Discover a world of difference at Worldwide! Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law. This is who we are. We’re a team of clinicians, scientists, and researchers who want to make healthcare better. We were founded on an unwavering commitment to authentic, personalized attention. And today, as CROs consolidate and the industry changes rapidly, that personalized attention is more important than ever. We all came to this industry for different reasons, from different walks of life. If you ask any one of us why we’re here, you’ll get a different answer. And that’s what makes us special. Not finding the right fit? Let us know you're interested in a future opportunity by clicking Get Started below or create an account by clicking 'Sign In' at the top of the page to set up email alerts as new job postings become available that meet your interest!
What you'll do
- Plan, implement and monitor study supply strategy and overall supply chain strategy to maximize efficiency and productivity.
- Optimize supply levels to ensure continuity while minimizing carrying costs.
- Control manufacturing and delivery processes and collaborate with Project Management, Vendor Management, and DLS Leadership.
- Develop and maintain detailed inventories of study drug and develop procedures to increase efficiency throughout the supply chain while ensuring quality and safety.
- Define and implement key supply chain KPIs at study and functional levels; identify process bottlenecks and implement solutions.
What they require
- Bachelor’s Degree in Life Science or Clinical Supply Chain Management or a similar relevant field
- Clinical research setting experience required (1 year minimum)
- Clinical supply chain operations experience required (1 year minimum)
- Preferred: Hands-on experience with supply chain functionality in an IRT system
- IT literacy, skills in Excel and the ability to handle electronic data
Global, midsize CRO with over 3,500 experts focused on clinical trials and drug development.
What people say about this company
2.8/ 5
- Mixed reviews on management effectiveness.
- Some employees enjoy the collaborative work environment.
- Concerns about workload and work-life balance.