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Chiyoda, Japan
… as new data becomes available and re-assesses as necessary Provides input into strategy with respect to clinical study design for local studies. (Provides input into global clinical studies with Japanese requirement if …
Chiyoda, Japan
Johnson & Johnson Innovative Medicine is recruiting for a Senior Document Specialist, Document Publishing Solutions (DPS), located in the Tokyo office, Japan. DPS is a global team that …
Mumbai, India
MAIN RESPONSIBILITIES • As the Specialist in the Medical Affairs Sub-Function, considered as highly experienced and knowledgeable resource within the …
Durham, North Carolina, United States
Pay posted by employer$68,400–$171,000
Overview: The Site Investigational Product Specialist (SIPS) will serve as a subject matter expert for nursing administration as it relates to the process and …
Sofia, Bulgaria
Summary An excellent opportunity for students eager to launch their Clinical Research careers while gaining practical experience in Clinical Trial Agreement support, Contract …
Shanghai, China +1 location
Clinical Trials Co-chairs clinical study team and works collaboratively with other study team members. Point of …
Beijing, China +1 location
Clinical Trials Co-chairs clinical study team and works collaboratively with other study team members. Point of …
Shanghai, China +1 location
… Johnson & Johnson Innovative Medicine is recruiting for a Associated Medical Director / Medical Director - Clinical Research. They will be a member of a matrix team dedicated to the implementation of clinical research …
Sofia, Bulgaria
… teams. Ensure all work is conducted in accordance with standard operating procedures, policies, good clinical practices and applicable regulatory requirements. Meeting quality and timeline metrics. Essential Functions …
Shanghai, China
RESPONSIBILITIES: Provide technical support for HCP initiated clinical study Make appropriate product and procedural recommendations and work closely with doctor/patient related …
São Paulo, Brazil
Responsible for investigator site management and monitoring for assigned sites: Clinical Trial Monitoring • Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan …
Budapest, Hungary
Negotiate clinical trial contracts with research sites, ensuring agreements are completed on time and meet quality and …
Amsterdam, The Netherlands
Why Join Clinical Functional Service Partnerships (CFSP)? At IQVIA, our Clinical Functional Service Partnership (CFSP) model …
Bratislava, Slovakia
… teams. Ensure all work is conducted in accordance with standard operating procedures, policies, good clinical practices and applicable regulatory requirements. Meeting quality and timeline metrics. Essential Functions …
Remote, North Carolina, USA +4 locations
Pay posted by employer$100,000–$120,000 USD per year
About the Role Help shape how patients find, access, and stay engaged in clinical trials around the world. PPD, the clinical research business of Thermo Fisher Scientific, is transforming …
Hyderabad, India
… while transforming your career. Job Description We are looking for a talented individual to join us as a Study Designer and Edit Check Programmer, reporting directly to the Sr. Manager, Clinical Systems and Analytical …
Hyderabad
… oversight, and continuous improvement of local laboratory reference range data management supporting our clinical development portfolio. In this role, you will oversee the end-to-end local laboratory data process, …
Bengaluru, India +1 location
… have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our expert team, you’ll have the opportunity …
Beijing, China +1 location
Position Summary: The Sr Local Trial Manager (Sr LTM) is responsible for local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. The Sr LTM is the primary …
Taipei, Taiwan
… Create and/or review technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Provide specialist regulatory and technical scientific support to …
Location reference: GeoNames (CC BY 4.0), normalized by Referizz.
