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Syneos HealthVer más

addressDirecciónSpain-Europe - ESP-Home-Based (Madrid), Spain
CategoríaCiencias sociales

Descripción del trabajo

Description

Clinical Trial Supplies Manager (Master Planner)

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.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

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. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.

CTSM(Master Planner)

The Master Planner (MP) is responsible to manage schedule and coordinate supply activities required to deliver clinical studies on time from drug product production to packaging product release.

Key Responsibilities

  • Develop and manage a planning schedule detailing all tasks required and when they should be completed by to meet study clinical needs and company targets within Platos (SAP planning tool)
  • Understand capacity management in system and operational relationship into PLATOS. Manage load leveling and bottleneck scheduling
  • Liaise with suppliers, and all the stakeholder of clinical studies (Clinical supply manager, QA stakeholder, labelling team , etc) to ensure tasks will be completed on time
  • Monitors project's progress to ensure it is following the schedule
  • Lead and coordinate operational meetings with several levels of management
  • Troubleshoots problems that occur during such as capacity issues, delays in activity completion and provide with appropriate action plan and impact on the overall planning
  • Collects and assesses data about the production and team's performance
  • Prepare reports about processes for upper management and suggests ways to improve efficiency

Qualifications

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%)

Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health

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.  Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description.  The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above.   Further, nothing contained herein should be construed to create an employment contract.  Occasionally, required skills/experiences for jobs are expressed in brief terms.  Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.  The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Refer code: 701171. Syneos Health - El día anterior - 2024-02-17 00:28

Syneos Health

Spain-Europe - ESP-Home-Based (Madrid), Spain

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