Nos aseguraremos de que las personas con discapacidades reciban adaptaciones razonables para participar en el proceso de solicitud de empleo o entrevista de trabajo, para que puedan ejercer las funciones de trabajo esenciales y recibir otros beneficios y privilegios del empleo. Comuníquese con nosotros para solicitar una adaptación.
Project Manager - Global Clinical Supplies
Share job link
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Locations considered:
Bulgaria, Croatia, Greece, Hungary, Kenya, Latvia, Poland, Romania, Serbia, South Africa, Turkey, Ukraine
*Remote/Office/Hybrid*
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
We have a vacancy for Project Manager/Sr Project Manager to join our Global Clinical Supplies Team in the EMEA region. This can be office based, hybrid, or fully homebased in a number of EMEA locations (note that level will be decided after interview depending on skills/competencies).
Role Overview
Manages full supply chain oversight for complex global clinical trials. Ensures project/study activities are in compliance with company and client requirements.. Acts as a department representative on all assigned projects and provides consultation services to clients.
A day in the life:
Develops study specific plans for each assigned project.
Meets with internal teams to coordinate efforts, provide recommendations and risks, and update project reports/spreadsheets.
Integrates all clinical supplies activities into the supply chain to support project logistic strategy and compliance with GxP requirements.
Participates in ongoing training on new regulations.
Represents the department internally and externally at meetings, strategic projects and initiatives as per the business requirements.
Mentors and guides supports junior team members.
Participates in process improvement initiatives.
Maintains and uses existing tools while continously looking for improvement opportunities
May participate in the bidding and/or bid defense opportunities
Client contact for their supply chain strategy/requests/questions/concerns Participates in ongoing training on new regulations
Education and Experience:
Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5 (PM) 8+ (SrPM) years). Preferably eith experience of clinical supplies in a clinical trial environment.
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:
Excellent English and communication skills both written and verbal
Excellent interpersonal, planning, organizational, problem solving, sense of urgency and decision making skills.
Demonstrated leadership and team building skills
Strong working knowledge of Microsoft Office suite
In-depth focus on customers and attention to detail
Ability to work in team environment, as well as work completely independent
Comprehensive understanding of clinical supply operation
Strong client building and 3rd party relationship management
Outstanding ability to provide customer service with the highest standards of quality and excellence
Skillful in bid preparation and bid defense
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Apply today! http://jobs.thermofisher.com
Recibe notificaciones de trabajos similares
¡Error!
Recomendaciones de perfil
Trabajos similares
-
Associate Project Manager - Global Clinical Supplies
Id. del empleo R-01305745
Integrates all clinical supplies activities into the supply chain to support project logistic strategy and compliance with GxP requirements. We require experience working in a clinical trial environme...
-
Clinical trial coordinator - FSP
Id. del empleo R-01306115
CTC works cross-functionally, with internal and external partners, on clinical study management activities, as agreed with the Study Delivery Lead, for in-house and outsourced studies across all phase...
-
Clinical Trial Coordinator I/II
Ubicación Sofia, Bulgaria Id. del empleo R-01301966
Performs investigator file reviews and logging of outstanding issues in project related tracking tools. Project administration. Disseminates study related information, including project tracking updat...
-
Clinical Trial Coordinator, Athens/Thessaloniki
Ubicación Athens, Grecia Id. del empleo R-01269537
Shown ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspect...
-
Sr Clinical Trial Coordinator
Ubicación Belgrade, Serbia Id. del empleo R-01305930
Supports the maintenance of study specific documentation and global support with specific systems, tools and trackers including but not limited to: study team lists, tracking of project specific train...
-
Clinical Trial Coordinator- Client- dedicated
Ubicación Athens, Grecia Id. del empleo R-01295867
Performs administrative tasks on assigned trials, including, but not limited to, timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, distributing mass mailings...
-
Clinical Trial Coordinator (Encouraging Applications from Disabled Individuals)
Ubicación Istanbul, Turquía Id. del empleo R-01299221
Supports the maintenance of study specific documentation and systems including but not limited to: study team lists, tracking of project specific training requirements, system access management, and t...
-
Senior Medical Project Coordinator, EMEA
Id. del empleo R-01307151
Independently functions as the Project Lead for medical monitoring services when SAE case processing has not been contracted. Previous experience that provides the knowledge, skills, and abilities to...
-
Medical Project Coordinator, EMEA
Id. del empleo R-01307148
Reviews data for safety trends, coding consistencies, and potential follow up with investigator sites. Previous experience that provides the knowledge, skills, and abilities to perform the job (compar...
Los solicitantes de empleo también vieron
Nos aseguraremos de que las personas con discapacidades reciban adaptaciones razonables para participar en el proceso de solicitud de empleo o entrevista de trabajo, para que puedan ejercer las funciones de trabajo esenciales y recibir otros beneficios y privilegios del empleo. Comuníquese con nosotros para solicitar una adaptación.