Clinical Specialist Job at Worldwide Clinical Trials | Apply Now
Looking for a clinical specialist job in the life sciences field? This exciting remote job opportunity at Worldwide Clinical Trials offers professionals a chance to work with a global CRO and contribute to innovative clinical research. If you have experience in supply chain or clinical research, this life science job could be your next big career move.
Job Details
- Job Position: Clinical Supply Specialist
- Job Location: Remote job (Europe) – Virtual Poland, Virtual Croatia, Barcelona (Spain), Virtual United Kingdom, Tbilisi (Georgia), and other locations
- Job ID: JR101932
About the Organisation
Worldwide Clinical Trials is a global, midsize Contract Research Organization (CRO) with over 3,500+ professionals worldwide. The company is known for pushing boundaries and taking innovative approaches to improve patient lives. With a strong focus on collaboration, diversity, and creativity, Worldwide Clinical Trials offers a supportive environment where employees can thrive and grow in their careers.
Job Description
This clinical specialist job focuses on planning, implementing, monitoring, and improving supply chain strategies within clinical trials. The role involves working closely with Project Management, Vendor Management, DLS Leadership, Finance teams, and external vendors to ensure smooth supply chain operations.
This remote job is ideal for candidates with experience in clinical research or supply chain who want to grow in a global CRO environment while contributing to impactful life science jobs.
Qualifications
This Clinical Specialist job requires:
Educational
- Bachelor’s Degree in Life Science or a related field
ExperienceÂ
- Minimum 1 year experience in a Contract Research Organization (CRO)
- 1–2 years of experience in supply chain or clinical research (mandatory)
- Experience with IRT/RTSM systems is a plus
Skills
- Strong planning and organizational skills
- Logical and systematic approach to work
- Excellent time management and ability to meet deadlines
- Problem-solving and strategic thinking abilities
- Strong relationship management and collaboration skills
- Negotiation and influencing skills
- Business and analytical skills
- IT literacy, especially Excel and electronic data handling
- Understanding of risk management in supply chain
Key Responsibilities
The Clinical Specialist Job Role Responsibilities include:
- Plan, implement, and monitor study supply strategy to maximize efficiency and productivity
- Optimize supply levels to ensure continuity while minimizing costs
- Control manufacturing and delivery processes
- Collaborate with Project Management, Vendor Management, and DLS Leadership
- Develop and maintain detailed inventories of study drugs
- Improve supply chain procedures while ensuring quality and safety
- Define and implement key supply chain KPIs
- Identify process bottlenecks and implement timely solutions
- Perform additional related duties as assigned
Why Join Worldwide Clinical Trials?
- Work in a global CRO with a strong reputation
- Inclusive and diverse workplace culture
- Opportunity to work on innovative clinical trials
- Supportive leadership and collaborative teams
- A meaningful role contributing to improving patient lives
