Clinical Supply Specialist
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| Company Name | ACROA |
| Company Type | NGO |
| Job Type | Full-Time |
| Salary Range | Market Competitive |
| Location | Tirana, Tirana, Albania |
| Qualifications | Professional Certifications |
| Experience | No Experience / Fresh |
Job Overview
ACROA is seeking a Clinical Supply Specialist to join their team in Tirana, Albania. This entry-level role involves supporting clinical trials and ensuring compliance with Good Clinical Practice (GCP) and other essential regulations.
Company Overview
ACROA is dedicated to promoting Good Clinical Practice (GCP) and adherence to other vital regulations like GLP and GMP in clinical trials. The organization represents its members’ collective views on clinical research issues, following both national and international guidelines to ensure high standards in research services.
Quick Details
- Salary Range: Market Competitive
- Job Type: Full-time
- Qualifications: Professional Certifications
- Experience: No Experience / Fresh
Key Responsibilities
- Support the management and distribution of clinical trial supplies effectively.
- Ensure accurate inventory and meticulous tracking of all study materials.
- Collaborate with research teams to forecast and plan for supply needs.
- Maintain strict compliance with GCP, GLP, GMP, and other relevant regulations.
- Assist in the preparation and secure shipment of clinical samples and kits.
- Document all supply chain activities and related processes meticulously.
Requirements
- Basic understanding of Good Clinical Practice (GCP) principles.
- Strong organizational skills and exceptional attention to detail.
- Ability to work effectively and efficiently in a highly regulated environment.
- Excellent communication and collaborative teamwork abilities.
- Proficiency in basic office software applications.
- Willingness to learn and adapt to new clinical research processes and protocols.
Benefits
- Opportunity to work in the critical and evolving field of clinical research.
- Gain valuable experience with GCP and international regulatory guidelines.
- Structured professional development in a supportive and learning-focused environment.
- Contribute directly to advancements in health care and medical science.
- Engage in a collaborative and team-oriented work culture.
- Receive a competitive salary and comprehensive benefits package.