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Requirement for Clinical Logistics Specialist at PAREXEL
Posted May 2, 2011
· 1 - 3 Years
Organization
PAREXEL International is a growing, fast-paced, global Clinical Research Organization (CRO) that has helped bring to market 49 of the top 50 selling pharmaceuticals. In fact, we have worked with all 10 of the world's top 10 pharmaceutical companies.
Given our breadth of expertise and the trust placed in us by major pharmaceutical companies worldwide, PAREXEL can provide you with a number of career options in Clinical Research that can rarely be found within just one company. In fact, over 25% of the positions opened at PAREXEL are filled by current employees working to advance their skills and careers.
Given our breadth of expertise and the trust placed in us by major pharmaceutical companies worldwide, PAREXEL can provide you with a number of career options in Clinical Research that can rarely be found within just one company. In fact, over 25% of the positions opened at PAREXEL are filled by current employees working to advance their skills and careers.
Role
Designation Clinical Logistics Specialist
Job Description
The Clinical Logistics Specialist conducts logistics processes, in collaboration with other Clinical Logistics personnel, ensuring that projects are progressing and systems are set up and maintained according to quality standards, Standard Operating Procedures and applicable ICH-GxP* and other applicable local regulation and industry guidelines.
Key Accountabilities
- Oversees the logistics aspect of designated projects to ensure that the right supplies are delivered to the right locations at the right time and right conditions.
- Maintains strong focus on external and internal client satisfaction.
- Provides support for development of project specific logistics strategy.
- Executes clinical logistics procedures for clinical trials.
- Supports set-up of clinical trial logistics.
- Prepares and distributes study documents and materials.
- Performs day-to-day communication with the clinical team, sites and vendors.
- Participates in regular study team and client meetings, as required.
- Tracks and reports logistics study metrics to the project team.
- Supports financial control; tracks, checks and compiles invoices.
- Contributes to meeting study timelines and works efficient with systems in place.
- Supports central filing and final archiving activities.
- Complies with GxP* standards, including applicable Standard Operating Procedures (SOPs).
- Works toward and ensures he/she stays within budget / time allocated, in agreement with the applicable Clinical Logistics Services Manager and Clinical Logistics Leader.
- Travels as required by projects or Clinical Logistics Services activities.
- Uses a positive, objective, balanced, and result-driven approach.
- Participates in other Clinical Logistics Services project activities as required.
Clinical Trial Supply Services:
- Supervises shipments of medication in cooperation with drug depots, CRA's, investigators and courier service providers to and/or from sites.
- Executes processes for temperature control for Clinical Trial Supplies.
- Prepares documents for delivery to central file and product specification file.
- Organizes and supervises import / export and purchase of medication.
- Organizes re-labeling procedures for assigned projects.
- Organizes and supervises Clinical Trial Supplies destruction.
Desired Profile
Skills
- Understanding of the regulatory framework of drug development
- Multi-tasking and prioritization ability.
- Result-oriented, confident, self-motivated, and driven / high energy.
- Credible team player with good facilitation skills.
- Good interpersonal , verbal and written communication skills
- Solid communication (verbal & written) and negotiation skills. Ability to influence and gain collaboration from and respect of key stakeholders.
- Demonstrated ability to conduct business in English (written and spoken) and in local language if different from English.
- Practical understanding of the drug development regulatory framework.
- Good knowledge of Microsoft Office programs (Word, PowerPoint, and Excel).
- Strong client focus.
- Ability to build rapport with a culturally diverse group at multiple levels and disciplines.
- Flexible, capable of managing change and ambiguity.
- Good analytical capabilities combined with creative problem-solving skills and a sense of urgency.
Minimum Work Experience
- Experience in clinical logistics, or related field within the biopharmaceutical industry or in general logistics.
- Demonstrated multinational work experience.
Experience 1 - 3 Years
Industry Type Pharma/ Biotech/Clinical Research
Role Other
Functional Area Other
Education UG - B.Pharma,B.Sc - Biology, Microbiology, Nursing, Zoology,B.Tech/B.E. - Bio-Chemistry/Bio-Technology, Biomedical,BDS - Dentistry,BHM,MBBS - Medicine
PG - M.Pharma - Pharmacy,M.Sc - Any Specialization, Biology, Botany, Microbiology, Nursing, Zoology,M.Tech - Any Specialization, Bio-Chemistry/Bio-Technology, Biomedical,M.S/M.D - Cardiology, Dermatology, ENT, General Practitioner, Gyneocology, Hepatology, Immunology, Microbiology, Neonatal, Nephrology, Obstretrics, Oncology, Opthalmology, Orthopaedic, Pathology, Pediatrics, Psychiatry, psychology, Radiology, Rheumatology, Urology
Location Hyderabad / Secunderabad
Keywords Clinical Logistics, Pharma Depot, Pharmacist, World Courier, Clinical Trial Supplies, re - labeling
Contact PAREXEL International (India) Pvt Ltd
Website http://www.parexel.com
Job Description
The Clinical Logistics Specialist conducts logistics processes, in collaboration with other Clinical Logistics personnel, ensuring that projects are progressing and systems are set up and maintained according to quality standards, Standard Operating Procedures and applicable ICH-GxP* and other applicable local regulation and industry guidelines.
Key Accountabilities
- Oversees the logistics aspect of designated projects to ensure that the right supplies are delivered to the right locations at the right time and right conditions.
- Maintains strong focus on external and internal client satisfaction.
- Provides support for development of project specific logistics strategy.
- Executes clinical logistics procedures for clinical trials.
- Supports set-up of clinical trial logistics.
- Prepares and distributes study documents and materials.
- Performs day-to-day communication with the clinical team, sites and vendors.
- Participates in regular study team and client meetings, as required.
- Tracks and reports logistics study metrics to the project team.
- Supports financial control; tracks, checks and compiles invoices.
- Contributes to meeting study timelines and works efficient with systems in place.
- Supports central filing and final archiving activities.
- Complies with GxP* standards, including applicable Standard Operating Procedures (SOPs).
- Works toward and ensures he/she stays within budget / time allocated, in agreement with the applicable Clinical Logistics Services Manager and Clinical Logistics Leader.
- Travels as required by projects or Clinical Logistics Services activities.
- Uses a positive, objective, balanced, and result-driven approach.
- Participates in other Clinical Logistics Services project activities as required.
Clinical Trial Supply Services:
- Supervises shipments of medication in cooperation with drug depots, CRA's, investigators and courier service providers to and/or from sites.
- Executes processes for temperature control for Clinical Trial Supplies.
- Prepares documents for delivery to central file and product specification file.
- Organizes and supervises import / export and purchase of medication.
- Organizes re-labeling procedures for assigned projects.
- Organizes and supervises Clinical Trial Supplies destruction.
Desired Profile
Skills
- Understanding of the regulatory framework of drug development
- Multi-tasking and prioritization ability.
- Result-oriented, confident, self-motivated, and driven / high energy.
- Credible team player with good facilitation skills.
- Good interpersonal , verbal and written communication skills
- Solid communication (verbal & written) and negotiation skills. Ability to influence and gain collaboration from and respect of key stakeholders.
- Demonstrated ability to conduct business in English (written and spoken) and in local language if different from English.
- Practical understanding of the drug development regulatory framework.
- Good knowledge of Microsoft Office programs (Word, PowerPoint, and Excel).
- Strong client focus.
- Ability to build rapport with a culturally diverse group at multiple levels and disciplines.
- Flexible, capable of managing change and ambiguity.
- Good analytical capabilities combined with creative problem-solving skills and a sense of urgency.
Minimum Work Experience
- Experience in clinical logistics, or related field within the biopharmaceutical industry or in general logistics.
- Demonstrated multinational work experience.
Experience 1 - 3 Years
Industry Type Pharma/ Biotech/Clinical Research
Role Other
Functional Area Other
Education UG - B.Pharma,B.Sc - Biology, Microbiology, Nursing, Zoology,B.Tech/B.E. - Bio-Chemistry/Bio-Technology, Biomedical,BDS - Dentistry,BHM,MBBS - Medicine
PG - M.Pharma - Pharmacy,M.Sc - Any Specialization, Biology, Botany, Microbiology, Nursing, Zoology,M.Tech - Any Specialization, Bio-Chemistry/Bio-Technology, Biomedical,M.S/M.D - Cardiology, Dermatology, ENT, General Practitioner, Gyneocology, Hepatology, Immunology, Microbiology, Neonatal, Nephrology, Obstretrics, Oncology, Opthalmology, Orthopaedic, Pathology, Pediatrics, Psychiatry, psychology, Radiology, Rheumatology, Urology
Location Hyderabad / Secunderabad
Keywords Clinical Logistics, Pharma Depot, Pharmacist, World Courier, Clinical Trial Supplies, re - labeling
Contact PAREXEL International (India) Pvt Ltd
Website http://www.parexel.com