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Submissions Coordinator Jobs In China - 32 Job Positions Available

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1 – 20 of 32 jobs
IQVIA jobs

Responsibilities include, but are not limited to: • Trial and site administration: o Track (e.g. essential documents) and report o Ensure collation and distribution of study tools and documents • Document management: o Prepare documents and

IQVIA  26 days ago
Labcorp jobs

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology

Labcorp  13 days ago
Chinachem Group jobs

Job Overview Responsibilities Periodic review and audit of building services systems and building maintenance standard for recommending and implementing works including incorporation of new technologies and standards to maintain the required quality standards and conditions Provide

Chinachem Group  11 days ago
Novotech jobs

Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. Major Responsibilities Describe the tasks, duties, and responsibilities the employee who

Novotech  7 days ago
dsm-firmenich jobs

Job Title: Sales Account Coordinator City, Country: Shanghai, China Join the Global Consumer Business team in a role that keeps projects, customer relationships, and commercial activities moving forward. As a Sales Account Coordinator, you will work closely with

Dsm-firmenich  4 days ago
Centric Brands jobs

About Us Centric Brands is a leading lifestyle brand collective that designs, sources, markets and sells high quality products in multiple segments, including women’s, men’s and kid’s apparel, accessories, entertainment and beauty. Centric Brands is focused

Centric Brands  3 days ago
Fortrea jobs

Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation

Fortrea  28 days ago
PAREXEL jobs

When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every

PAREXEL  27 days ago
Fortrea jobs

Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation

Fortrea  27 days ago
Fortrea jobs

Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all

Fortrea  27 days ago
Fortrea jobs

Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all

Fortrea  26 days ago
Fortrea jobs

Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation

Fortrea  26 days ago
Kone jobs

• Project Admin is responsible for collecting information for Project Manager’s and Supervisor decision making • Monitors the project schedule (e.g. expiring S-plan milestones) for helping to maintain the project plan and notifies Project Manager about

Kone  21 days ago
AstraZeneca jobs

Serve as SDTL Responsible for planning and leading the delivery of all components of a clinical study to time, cost, and quality from Study Specifications (SS) through study closeout activities and Clinical Study Report (CSR). Form

AstraZeneca  20 days ago
Prudential plc jobs

Prudential’s purpose is to be partners for every life and protectors for every future. Our purpose encourages everything we do by creating a culture in which diversity is celebrated and inclusion assured, for our people, customers,

Prudential Plc  18 days ago
Hong Kong Baptist University jobs

LANGUAGE CENTRE Executive Officer (26270059) The appointee is expected to provide general administrative support to the Centre’s programmes, activities and projects. Responsibilities: Providing secretarial support to the Head of Language Centre, the Manager, and coordinators; Serving as

Hong Kong Baptist University  17 days ago
Roche jobs

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,

Roche  16 days ago
UN Women jobs

Background: UN Women, grounded in the vision of equality enshrined in the Charter of the United Nations, works for the elimination of discrimination against women and girls; the empowerment of women; and the achievement of equality

UN Women  14 days ago
Roche jobs

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,

Roche  14 days ago
Johnson & Johnson jobs

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our

Johnson & Johnson  12 days ago

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