Clinical Supply Support Specialist Services - Spain - FSP
WFA Digital Insight
The demand for skilled professionals in clinical supply chain management has grown significantly, with a 25% increase in job postings over the past year. As the pharmaceutical industry continues to evolve, companies like Parexel are looking for experts who can navigate the complexities of clinical trials logistics. With the shift towards remote work, this role offers a unique opportunity for candidates to work with a global company while leveraging their digital skills. According to recent statistics, 75% of clinical trial managers consider digital skills essential for success in the field. Before applying, candidates should be aware of the importance of attention to detail, analytical skills, and the ability to work in a fast-paced environment.
Job Description
About the Role
Parexel is seeking a Clinical Supply Support Specialist to join their team in Spain. As a key member of the clinical supply chain management team, you will be responsible for ensuring the efficient and timely delivery of clinical supplies to trial sites. Your day-to-day activities will involve coordinating with various stakeholders, including trial managers, suppliers, and logistics providers. You will be working closely with a team of experienced professionals who are passionate about improving the world's health through innovative clinical trials solutions.The clinical supply chain management team plays a critical role in ensuring that clinical trials are conducted efficiently and effectively. As a Clinical Supply Support Specialist, you will be responsible for managing the flow of clinical supplies, from procurement to delivery, and ensuring that all regulatory requirements are met. Your work will have a direct impact on the success of clinical trials and the development of new treatments for patients.
Parexel is a global company with a strong reputation for delivering high-quality clinical trial solutions. As a member of the Parexel team, you will have the opportunity to work with a diverse range of clients, from small biotech companies to large pharmaceutical organizations.
What You Will Do
- Manage clinical supply chain activities, including procurement, inventory management, and logistics
- Coordinate with trial managers, suppliers, and logistics providers to ensure timely delivery of clinical supplies
- Conduct risk assessments and develop mitigation strategies to ensure supply chain continuity
- Monitor and report on supply chain performance metrics, including inventory levels, shipment tracking, and delivery timelines
- Develop and maintain relationships with suppliers and logistics providers to ensure high-quality service and competitive pricing
- Collaborate with cross-functional teams, including clinical operations, regulatory affairs, and quality assurance
- Develop and implement process improvements to increase efficiency and reduce costs
- Participate in audits and inspections to ensure compliance with regulatory requirements
- Manage and maintain accurate and up-to-date records and documentation
What We Are Looking For
- Bachelor's degree in a related field, such as life sciences, logistics, or supply chain management
- At least 2 years of experience in clinical supply chain management or a related field
- Strong knowledge of clinical trials regulations and guidelines, including GCP and GDP
- Excellent communication and interpersonal skills, with the ability to work effectively with cross-functional teams
- Strong analytical and problem-solving skills, with the ability to develop and implement process improvements
- Experience with inventory management and logistics systems, including ERP and CRM software
- Strong attention to detail and organizational skills, with the ability to manage multiple tasks and priorities
Nice to Have
- Experience with clinical trial management systems, including CTMS and EDC
- Knowledge of pharmaceutical industry regulations and guidelines, including FDA and EMA
- Experience with lean sigma or other process improvement methodologies
Benefits and Perks
- Competitive salary and benefits package
- Opportunity to work with a global company and diverse range of clients
- Professional development and training opportunities
- Flexible working hours and remote work options
- Access to cutting-edge technology and systems
- Collaborative and dynamic work environment
How to Stand Out
- Develop a strong understanding of clinical trials regulations and guidelines, including GCP and GDP
- Highlight your experience with inventory management and logistics systems, including ERP and CRM software
- Emphasize your analytical and problem-solving skills, with examples of process improvements you have developed and implemented
- Prepare to discuss your experience working with cross-functional teams and developing relationships with suppliers and logistics providers
- Research Parexel's company culture and values, and be prepared to discuss how your own values and motivations align with those of the company
- Be prepared to provide specific examples of your experience with clinical trial management systems, including CTMS and EDC
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