Clinical Trials Jobs in Alīgarh
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Search Results - Clinical Trials Jobs in Alīgarh
Safeguard Global RecruitingAlīgarh
of project management principles, methodologies, and processes
KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED:
• At least 2 years’ experience working in clinical trials.
• Demonstrable experience in the management or coordination of clinical trials...
Era UniversityAlīgarh
measures
• Leading research initiatives, publications, and clinical trials in cardiology
• Participating in curriculum development, academic planning, and institutional committees
• Organizing and contributing to CMEs, conferences, and academic programs...
CytelAlīgarh
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.
Our values
• We...
VeramedAlīgarh
Purpose:
This function supports the protection of patient privacy when clinical trial data is shared externally.
Typical use cases: Regulatory submissions
Data sharing with researchers
Health authority requests
External collaborations
Clinical...
Safeguard Global RecruitingAlīgarh
on Protocol and CSR projects across all clinical trial phases and a variety of therapeutic areas.
• Passion for science and healthcare.
• Excellent computer skills including knowledge of Adobe, Internet software, Spreadsheet software, Word Processing software...
PDC CROAlīgarh
Pharmaceutical Development Company is a leading clinical research organization, providing a Full-Service End-to-End Solution for Phase I to IV clinical trials and NIS /RWE studies in the Middle East and Africa region.
Our clients include...
VeramedAlīgarh
of CDISC standards, and experience supporting NDA/BLA/MAA submissions.
Key Responsibilities:
• Lead statistical programming activities for ISS/ISE analyses and pooled clinical trial datasets.
• Design, develop, validate, and maintain integrated ADaM...
ACL DigitalAlīgarh
Statistical Programmer of Statistical Programming is responsible for all statistical programming aspects of one or more clinical trials of drug development plans. The position ensures drug development plans are executed efficiently, with timely and high...
IQVIAAlīgarh
if working knowledge with R software.
• Min. 3 years industry experience.
• Strong working knowledge of R software (important)
• Interest in PK/PD and clinical trial concepts.
• Studious and data driven person. Eye for detail is very important.
• Proficient...
Syneos HealthAlīgarh
in a clinical trial environment.
Excellent written and verbal communication skills.
Ability to read, write, speak and understand English.
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