...JOB DESCRIPTION
About therole:
The Clinical Programmer (SDTM) is primarily responsible for SDTM programming based on Clinical Protocols... ...& Experience:
Bachelor's Degree in Life ...
The Position
The Project Clinical Data Programmer Specialist is overall accountable and responsible for implementation and adherence to project standards template in EDC and DMW. Demonstrates subject matter expertise and equips in-depth knowledge and...
...is a leading company in the None industry, specializing in data research and analysis. Our team of experts delivers high-quality insights... ...industry.
Role And Responsibilities
As a ...
...trial activities for our medical device portfolio, ensuring compliance with international regulatory standards for markets including the U.S. and Japan. The role requires extensive experience in clinical trial manag...
...execution of clinical trials for our anti-diabetes and anti-cancer product portfolios. With a primary focus on developing innovative therapies to combat diabetes and cancer, you will play a pivotal role in revolutio...
...for CT under the EU Regulation.
Position Responsibilities
Manage the signing of clinical trial documentation such as powers of attorney, expected to be able to coordinate many signing at the same time.
Prov...
...from trial outline to Submission. Responsible for being the point of contact during Audits and Inspections for the respective allocated therapy/project area. Responsible for performing/implementing various tasks rel...
...As a Clinical Researcher, Your Main Responsibilities Are
Design and conduct clinical trials in the skin category such as Acne, Pigmentation, Atopic Dermatitis, Skin hydration, Skin Barrier function Anti-ageing.
...
...Tabulation Mode deliverables.
Active participation in sharing better practices on use of standards in alignment with Lead Clinical Data Programmer and Process & Automation Specialist.
Maintain system related d...
