16 jobs voor project manager clinical research gevonden

We'd love to find a.Clinical Project Manager to help us serve our sophisticated customers while adhering to our rigorous but sensible procedures...As a Cell.

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

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.

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.

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..

The main responsibility of the Proposal Coordinator is following up on the creation of budget quotations for our clients in response to Request for Proposals (RFP) and Change in Scope (CIS) requests.As Proposal Coordinator you bring together different operational teams to collect and process all necessary input for the development of your budget proposals while respecting deadlines and combining multiple simultaneous projects.By complying with our internal standards, you ensure we deliver polished and accurate documents to our clients.This is a detail-driven role and as such any successful candidate will bring a seasoned eye for detail and commitment to compliance with SGS Clinical Research processes and guidelines for budget development.

You will be part of a small but tight-knit team as part of a diverse organization in a fascinating industry.

Your responsibilities

• You act as the lead for assigned budget requests, in response to RFP and CIS requests.
• You identify the internal or external client's requirements and you interact with business development and the operational teams to obtain input for your budgets.
• You set up budgets (ballparks, detailed budgets, client-specific bid grids) for our various clinical conduct services, including our early phase clinical sites, biometrics activities and clinical operations.
• You take care of all necessary administrative proceedings.
• You establish and adhere to timelines for completion of deliverables in cooperation with the sales team and/or the operational teams.
• You ensure clear and open communication towards upper management, the sales team and the applicable operational team members (and occasionally our clients).
• You review, verify, and evaluate cost estimates to ensure agreement with written information, client specifications and internal assumptions.
• You conduct quality control measures to ensure the final budget meets the company and departmental standards.
• You interact with the other Proposal Development team members to ensure alignment on processes, transfer and sharing of expertise and knowledge, and to develop the department's improvement projects.

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.

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:

.The Client Services (CS) team at the Antwerp Cell.

Our client is a growing research laboratory specializing in the field of immune oncology.They mainly collaborate with pharmaceutical and biotechnology companies in the research and development of innovative new drugs for the treatment of cancer..

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.

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.

Are you looking for an exciting new opportunity?Cell.Carta, a renowned Contract Research Organization, is actively seeking a highly skilled and motivated.Medical Writer to join our dynamic team.

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.

Are you looking for an exciting new opportunity?Cell.