Principal Analyst

buscojobs España; Madrid; A distancia; EUR 50.000 - 75.000; Jornada completa

Descripción de la vacante

A leading biopharmaceutical organization is seeking a Clinical Trial Supplies Manager specializing in cold chain logistics. You will be responsible for managing the integrity of cold chain processes, ensuring compliance with regulatory requirements, and coordinating with multiple stakeholders. This role provides an opportunity to significantly impact the successful execution of clinical trials across diverse locations, contributing to better patient outcomes.

Formación

• Bachelor's degree or equivalent in relevant field.
• Experience in CRO, pharmaceutical, or biopharma project management.
• High competency in English.

Responsabilidades

• Manage the integrity of cold chain logistics for clinical trials.
• Oversee storage and distribution processes.
• Address temperature excursions during clinical studies.

Conocimientos

Strong organizational skills

Excellent communication

Ability to manage time

Flexibility

Educación

Bachelor's Degree in Life Sciences, Medicine, Pharmacy, Nursing

Herramientas

MS Office Applications

Descripción del empleo

Clinical Trial Supplies Manager (Cold Chain)

• Homebased EMEA

Updated : February 20, 2025

Location : Spain-Europe - ESP-Home-Based (Barcelona)

Job ID : 25001871

Clinical Trial Supplies Manager - Cold Chain

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Discover what our 29,000 employees, across 110 countries already know : WORK HERE MATTERS EVERYWHERE.

Why Syneos Health :

• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
• We are continuously building the company we all want to work for and our customers want to work with.

Job responsibilities :

The Third-Party Support Manager – Cold Chain is responsible to oversee and manage the integrity of the cold chain logistics processes, ensuring that vaccines are stored and transported within approved temperature ranges, and to promptly address and resolve any temperature excursions during clinical studies.

Key Responsibilities :

• Master Cold Chain activities related to storage and distribution
• Be responsible for performance management monitoring and reporting (KPI, monthly)
• Ensure correct application of the procedures through ad-hoc training worldwide (local depots, vaccination center, CMO, etc.)
• Identify and share good practices
• Manage Cold Chain Temperature Excursion, deviation, CAPA
• Support Cold Chain Change Control and Risk Assessment
• Support GSK Vaccines sites in the implementation of Cold Chain requirements
• Participate in all meetings that are part of the Cold Chain management, both internally (Business Partners & Global functions) and with the external suppliers, to ensure a good operational progress
• Ensure visibility is given on demand and supply information across the supply chain to ensure pro-active management
• Support SME Cold Chain to feed process & tool improvement / automation opportunities
• Ad hoc projects contribution
• Collaborate with QA team to ensure compliance to cGMP
• Proactive view on critical risks and ownership of mitigation defined

What we're looking for :

• Bachelor's Degree (or equivalent) level of qualification in Life Sciences, Medicine, Pharmacy, Nursing or related field equivalent
• Prior experience in a contract research organization (CRO), pharmaceutical, or biotechnology company in project management or clinical trial supplies management
• Strong knowledge of Good Clinical Practice, ICH guidelines, Good Manufacturing Practices and other applicable regulatory requirements
• Strong organizational skills
• Strong ability to manage time and work independently
• Excellent communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince and persuade
• Flexibility and ability to handle multiple tasks to meet deadlines while delivering high quality work in a dynamic environment
• High level of competency in English language
• Proficiency with MS Office Applications
• Ability to travel as necessary (up to 25%)

Additional Information :

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities.

At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. If your past experience doesn't align perfectly, we encourage you to apply anyway. We also encourage you to join our Talent Network to stay connected to additional career opportunities.

Discover what our 29,000 employees already know : work here matters everywhere. A career with Syneos Health means your everyday work improves patients' lives around the world.

Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status.

J-18808-Ljbffr

J-18808-Ljbffr