Data Entry 招聘 在 Beijing (Peking) - 21 Job Positions Available

Job Description The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under the supervision of a Global Pharmacovigilance

Job Description The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under the supervision of a Global Pharmacovigilance

Company Description Do you want to develop your career and make an impact in the fast-growth, fast-moving B2B technology space? At Informa TechTarget, you’ll collaborate and grow alongside some of the industry’s most respected experts. You’ll

Job Description The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under the supervision of a Global Pharmacovigilance

Job Description The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under the supervision of a Global Pharmacovigilance

Clinical Research Associate, Beijing, office base ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on

Job Description SummaryRotational Engineering Leadership program committed to growing GEHCs entry level, high potential talent-people with a passion for technology, a drive for technical excellence, professional skills and GEHC values-by accelerating their development through intense technical training

BandLevel 3 Job Description SummarySite relationship management role to ensure sustainable trial execution at Site. Performs on-site and remote monitoring activities related to initiation, conduct and timely completion of Phase I-IV GDD trials within the country

公司描述 We take care of our employees, and they take care of our customers! Become a member of a global community! The international logistics industry is an integral piece of the global trade puzzle; we make

Job Overview: The Contracts Specialist II (CS II) works in collaboration with project teams and the Contracts Lead (CL) to perform key study start-up tasks related to site contracts in their country, or countries, of expertise.

Job Description:Essential Job Functions:•Collaborate with the team to contribute to the design of solutions addressing clients technology challenges.•Analyze data to derive insights, inform solution recommendations, and support strategic decision-making.•Assist in building and maintaining client relationships, understanding their

Clinical Site Associate, Beijing, 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, agility,

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

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

Job Title: Clinical Research Associate Job Location: China Job Overview: The CRA monitors investigational sites to ensure subject safety and provide quality data review and reporting in compliance with the Caidya and/or client Standard Operating Procedures (SOPs),