34 jobs voor clinical support manager gevonden

You will provide organizational and administrative support to Clinical Oncology teams located in multiple countries in Europe:

- general administrative support,

- mail and calendar management,

- arrange travel and expense reporting (using Concur system),

- expense booking

Bedrijfsprofiel:

VOOR JANSSEN PHARMACEUTICA, ONDERDEEL VAN JOHNSON EN JOHNSON CAMPUS BEERSE, ZIJN WIJ OP ZOEK NAAR:

As a Project Manager you support the business with their technology needs and requests, and you coordinate the Information Technology related projects.

You coach and advise multidisciplinary teams turning their business ideas and needs into products and solutions.

You keep all stakeholders well informed, and you collaborate closely with the business, vendors, local and global IT teams.

Your challenges and responsibilities:

• As a Project Manager you are involved from inception to completion, including needs assessment, solution exploration (with a keen eye on cost implications), implementation, and handover to the support team.
• You create a detailed project planning, update the planning when required, follow the budget and make sure progress is made.
• You organize and lead project meetings with all stakeholders to keep them informed.

Clinical Pharmacology and Pharmacometrics (CPP) is an integrated part of the Global Development organization within Johnson & Johnson Innovative Medicines.We work in cross disciplinary compound development teams and apply clinical pharmacology principles and pharmacometrics methodologies across the R&D portfolio to enable optimal decision making in drug development at the earliest time point and in the most efficient manner.CPP Summer Internships are available for Pharm.

.Create and update study documentation on project(s).Report metrics and data trends on project(s).Identify data conflicts and issues on project(s).

Job Summary.Medpace Reference Laboratories (MRL) is a full service central clinical trial laboratory offering project management, laboratory services, data management, logistics, and sample management and archiving capabilities, and quality assurance..

Job Summary.Medpace Reference Laboratories is a global, full service central clinical trial laboratory specializing in a multitude of therapeutic areas.

Your unique talents and perspective can make a vital contribution to innovative products that improve the lives of

people everywhere.Career opportunities within Johnson & Johnson companies may provide you with an ideal

setting to build your leadership experience, express your passion, and touch the world.

Janssen Research & Development aims to transform patients' lives by discovering and developing innovative

solutions to address the most important medical needs of our time.Within the Janssen R&D Finance

organization,

Global Development group together with around¿ 9000¿ internal and external colleagues from across the globe, we

manage clinical sites¿ and the execution of clinical trials, lead the operational delivery of clinical R&D trials and

programs, transform data into information to build knowledge, deliver the medical affairs portfolio & pre-approval

access and implement a great variety of¿ clinical operations processes and systems.

Key responsibilities of the role include:

- Supporting Affiliate funding process including Quarter close Journal Entry posting

- Supporting Flex process with reconciliation and Journal Entry posting

- Time compliance reports ¿ sharing the reports with the finance team.

- Travel&Entertainment expense reporting for Global Development organization

- Headcount management on ad-hoc basis for Global Development

- Creation of new cost centers, Non-Development projects codes and overall master data transactions

- Assisting reporting activities.

Bedrijfsprofiel:

VOOR JANSSEN PHARMACEUTICA, ONDERDEEL VAN JOHNSON EN JOHNSON CAMPUS BEERSE, ZIJN WIJ OP ZOEK NAAR:

As a Key Account Manager, you will focus on a select number of identified key/strategic clients and work to embed and grow business opportunity from a global SGS Clinical Research perspective.You will act as the point of contact between the client and the SGS Clinical Research Organization.

Your key responsibilities are:

• Build and maintain strong relationships with key clients, serving as their primary point of contact for all business-related matters.
• Develop and implement strategic account plans to achieve sales targets, foster account growth, and identify new business opportunities.
• Conduct regular business reviews with clients to assess their needs, address concerns, and provide solutions that meet their objectives.
• Collaborate with cross-functional teams to ensure seamless delivery of services and exceptional customer experience.
• Identify upselling and cross-selling opportunities within existing clients to maximize revenue generation.
• Stay updated on industry trends, market conditions, and competitor activities to proactively identify potential threats and opportunities.
• Prepare and present reports on account performance, sales forecasts, and market insights to internal stakeholders.
• Manage contract negotiations, renewals, and pricing discussions in collaboration with the SGS business development & support team
• Provide exceptional customer service by promptly addressing customer inquiries, resolving issues, and coordinating with internal teams to deliver timely solutions.
• Work collaboratively with SGS colleagues across the organization to ensure they are engaged and aligned to the account strategy and support new business opportunities within clients.

CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry.

Global Planview Adaptive.Work Administrator.Summary.The Global Planview Adaptive.

The Production Quality Assurance (PQA) Engineer manages quality activities within the Production Line to guarantee deployment of production quality strategy..1.

PPD Global Central Labs is a central laboratory to support clinical studies in the pharmaceutical industry.We are looking for a colleague to strengthen our team..Tasks..

.Lead, direct, coach, and develop an effective Warehouse Operations team responsible for all inbound, outbound, material receipt & inventory management, and distribution processes for raw materials and final drug products..

Your responsibilities include ensuring timely support for clinical and commercial readiness while maintaining the highest quality and safety standards.BedrijfsomschrijvingOur client is on a mission to revolutionize healthcare by combatting life threatening diseases with groundbreaking biotechnology.Situated in the vibrant heart of New Jersey, their global influence extends far and wide as they pioneer advanced cell therapies across various technology platforms.

You support the Business Development Managers by expanding the Clinical Research client base.You will identify new prospecting opportunities and actively reach out to understand their development needs.Close collaboration with the Business Development Managers will be required to create a plan to enhance new account penetration.You will be actively sourcing and calling on new accounts and scheduling meetings for the Business Development Managers, contributing to the growth of the client base and the health of the sales pipeline.

Responsiblities:

• Develop a sales methodology and strategy for increasing new account penetration
• Initiate outbound and respond to inbound sales calls, qualify leads, reach out to prospective clients and schedule meetings for the Business Development Managers
• Maintain frequent email and phone contact with prospective clients to grow and expand business relationships.
• Generate client interest for SGS webinars, company updates and conferences
• Maintain and manage the CRM database with all sales activity.
• Attend internal business development calls and meetings to discuss new opportunities and the overall sales pipeline
• Provide general intelligence on key competitors.
• Collaborate effectively with Business Development Managers from other SGS Health & Nutrition business units to bring potential opportunities to their attention.
• Leverage Social Selling techniques and tools to reach clients through digital channels sharing information

• Contribute to the implementation of a cutting-edge payroll software.
• Ensure the accurate compensation of both employees and medical staff.
• Provide administrative support to your colleagues, handling thematic leaves, sabbaticals, and other social documents.
• Facilitate seamless communication between the Accounting and Personnel Departments.

Medpace Laboratories is een centraal labo ter ondersteuning klinische studies pharmaceutische industrie.Wij zijn gevestigd industriepark Heverlee en zoeken enthousiaste Administratief medewerker ter ondersteuning van project management team.

We, at Sanofi, are there beside people in need, as a health journey partner+100,000 employees, representing 142 nationalities90 countries where Sanofi is present, providing healthcare solutions in 170 countries69 manufacturing sites in 32 countries21 Research and Development sites comprising medicines, clinical research and vaccinesJobomschrijvingThe MSAT Scientist is a member of the Analytical Science and Technology (AST) team in the Recombinant Mammalian Drug Substance (DS) function within the global Manufacturing Science, Analytics and Technology (MSAT) organization and is based in Sanofi Geel biopharmaceutical manufacturing site The Recombinant Mammalian DS platform function within global MSAT is the owner of Life Cycle Management of mammalian cell culture based DS Processes within Sanofi biologics manufacturing network.We deliver innovative, robust, and cost effective next generation processes, enable launch of new products, and provide commercial manufacturing/Quality Control support.

We, at Sanofi, are there beside people in need, as a health journey partner..+100,000 employees, representing 142 nationalities.90 countries where Sanofi is present, providing healthcare solutions in 170 countries.

The Analytical function within global Manufacturing Sciences, Analytics and Technology (MSAT) is responsible for method development and supports method validation, all part of the Analytical Life Cycle Management (ALCM), within Sanofi Biologics network.We deliver innovative, robust, and cost effective next generation analytical methods.

The MSAT Scientist is a member of the Analytical Science and Technology (AST) team in the Recombinant Mammalian Drug Substance (DS) function within the global Manufacturing Science, Analytics and Technology (MSAT) organization and is based in Sanofi Geel biopharmaceutical manufacturing site..The Recombinant Mammalian DS platform function within global MSAT is the owner of Life Cycle Management of mammalian cell culture based DS Processes within Sanofi biologics manufacturing network.

The TMF Records Specialist is a member of the core trial team and is responsible to provide operational expertise to the core trial team, oversees the implementation of the (Trial Master File) TMF strategy for the trial and supports the core trial team in all aspects of TMF management and in inspections or audits.The TMF Records Specialist provides and maintains oversight and guidance related to TMF activities throughout the course of the trial, to safeguard the protection of the trial subject, reliability of the trial results, compliance with study protocol, ICH GCP and applicable regulations and ensure inspection readiness at all times.The TMF Records Specialist closely collaborates with the core trial team to create, implement and maintain the list of trial specific expected records.This includes the identification of all relevant trial level records required to reconstruct the trial, independent of owner or system hosting the record.In this role you are responsible for the planning, tracking, formal QC and filing of all TMF trial level records according to internal and external standards and also to initiate the close out of the TMF.

Onze klant, Legend Biotech, gevestigd in Zwijnaarde, is een wereldwijd biotechnologiebedrijf dat de innovatieve CAR T celtheraptie naar Gent brengt.Het Legend Biotech team maakt hiermee dagdagelijks het verschil in het leven van vele patiënten die lijden aan kanker en andere levensbedreigende ziektes..

Our client, Legend Biotech, based in Zwijnaarde, is a global biotechnology company bringing the innovative CAR T cell therapy to Ghent.With this, the Legend Biotech team makes a daily difference in the lives of many patients suffering from cancer and other life threatening diseases..

Onze klant, Legend Biotech, gevestigd in Zwijnaarde, is een wereldwijd biotechnologiebedrijf dat de innovatieve CAR T celtheraptie naar Gent brengt.Het Legend Biotech team maakt hiermee dagdagelijks het verschil in het leven van vele patiënten die lijden aan kanker en andere levensbedreigende ziektes..

The CAR T Operations Supervisor is an exempt level position working within Technical Operations team, responsible for directing the daily production of a personalized cell therapy to support both clinical and commercial requirements in a sterile c.GMP environment.

Join our client’s team and play a crucial role in their cutting edge biotechnology advancements..As a CAR T Operations Technician, you'll be responsible for conducting essential CAR T process operations while ensuring compliance with safety policies and quality standards.

As a CAR T Operations Supervisor, you are responsible for the daily production process of personalized cell therapy, both for clinical and commercial purposes, in a sterile c.GMP environment.