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Junior Study Jobs In - 49 Job Positions Available

1 – 20 of 49 jobs
Tate & Lyle jobs

As the Associate Principal Scientist - Sensory, you are part of the Global Science & Innovation Team and play a key role in partnering with Technical Service team in APAC, Global applications & Ingredient Science with

Tate & Lyle  21 hours ago
Thermo Fisher Scientific jobs

Work Schedule Environmental Conditions Job Description Join us as a Project Manager - Labs – make an impact at the forefront of innovation. The Project Manager - Labs monitors and manages all aspects of designated clinical

Thermo Fisher Scientific  28 days ago
AstraZeneca jobs

The Bioanalysis Laboratory supports AstraZeneca R&D China by generating quality-compliant PK, PD, ADA, NAb, and biomarker data for cell therapy projects, biotherapeutic development and regulatory filing. The Associate Principal or Principal Bioanalysis Scientist is responsible for:

AstraZeneca  27 days ago
Gilead Sciences jobs

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives

Gilead Sciences  26 days ago
Amazon.com jobs

Amazon China is an inventive research and development company that designs and engineers high-profile consumer electronics products, like the Kindle, Kindle Fire, Fire TV, and Echo, etc. The products we design and engineer are easy-to-use and

Amazon.com  24 days ago
AstraZeneca jobs

Typical Accountabilities: Takes medical responsibilities to ensures successful conduct and integrity of all in-scope clinical studies Work as China study physician in China-join global studies, PK studies or country-specific clinical initiatives under the supervision from program/study lead physicians. Contributes to study design

AstraZeneca  21 days ago
AstraZeneca jobs

JOB REQUIREMENTS: Academic / Professional Qualification / Working Experience * Advanced SAS programming knowledge * 2 or 5+ years of working experience in Pharmaceutical industry * BSc or higher degree in Mathematical, Statistical, Computer Science or

AstraZeneca  21 days ago
AstraZeneca jobs

Responsible for providing technical leadership as compound or indication lead within a cross-functional team to design, execute, analyse and interpret clinical studies. Ensures projects (including multiple studies) adhere to Good Clinical Practice and regulatory requirements. Typical Accountabilities Provides

AstraZeneca  19 days ago
Novotech jobs

Responsible for day-to-day data processing operations for data management projects, including CRF (or other study data document) tracking, entry, and filing. Provides administrative and project management support to CDMs for data management projects as required, including creation

Novotech  15 days ago
Novotech jobs

Purpose of Pharmacovigilance Associate Role: The purpose of the Pharmacovigilance Associate role is to monitor and manage the safety aspects of clinical studies/post-marketing surveillance including but not limited to monitoring safety mailbox, preparation of safety management plan,

Novotech  15 days ago
ICON plc jobs

Informed Consent Specialist II, China, office based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration,

ICON Plc  11 days ago
Carrier jobs

Build a career with confidence Carrier Global Corporation, global leader in intelligent climate and energy solutions is committed to creating solutions that matter for people and our planet for generations to come. From the beginning, weve

Carrier  11 days ago
Syneos Health jobs

Site Contracts Specialist II/Sr - China Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping

Syneos Health  10 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 of

Fortrea  8 days ago
Biogen jobs

The Lead, Medical Writing in collaboration with global medical writing team and China CPT is responsible for the creation of medical writing deliverables for China, ensuring the high-quality, timely, and efficient development of clinical and regulatory

Biogen  7 days ago
Hatch jobs

Requisition ID: 100304 Job Category: Engineering Location: Shanghai, 31, China Join a company that is passionately committed to the pursuit of a better world through positive change. With more than 70 years of business and technical

Hatch  7 days ago
Onsemi jobs

Job Purpose · Ag Sintering Process Development for Power Module and Discrete with SiC · New Process and Package Development for High Power Discrete and Module Package · New Sintering Material Development for Discrete and Module

Onsemi  7 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  6 days ago
Danaher jobs

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At SCIEX, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all

Danaher  6 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  5 days ago

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