Clinical Trials Jobs in Meerut
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Search Results - Clinical Trials Jobs in Meerut
ProductLife GroupMeerut
Education & Experience
• Doctor or pharmacist by training
• Minimum 4 years experience working for service providers performing QC of case
• Minimum 3 years of experience in processing Clinical Trial cases.
• SafetyEasy/ Argus database experience
Profile...
Safeguard Global RecruitingMeerut
and implementation of project management methodologies and processes.
Responsibilities
3. 5 years industry experience including at least 1 year in Project Management roles in clinical trials within a CRO, pharmaceutical or biotech setting.
Good knowledge of the drug...
Proxima Skills AcademyMeerut
will support clinical data review and data validation activities to ensure accuracy, completeness, and consistency of clinical trial data. Daily responsibilities include performing data checks against study protocols, documenting and resolving data...
Era UniversityMeerut
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...
Proxima Skills AcademyMeerut
should possess skills in study design and conduct, including Protocol and Clinical Trials.
• Candidates should possess skills related to participant engagement and ethics, including Informed Consent.
• Relevant educational background in Life Sciences...
CytelMeerut
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...
Safeguard Global RecruitingMeerut
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...
ACL DigitalMeerut
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...
Safeguard Global RecruitingMeerut
Management roles in clinical trials within a CRO, pharmaceutical or biotech setting'
• Good knowledge of the drug development process, associated regulatory and ICH GCP guidelines and their application to clinical trials.
• Detailed and proactive approach...
Syneos HealthMeerut
in a clinical trial environment.
Excellent written and verbal communication skills.
Ability to read, write, speak and understand English.
CytelMeerut
that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials.
Responsibilities
As a Principal Statistical Programmer, your...
VeramedMeerut
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...
Safeguard Global RecruitingMeerut
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 CROMeerut
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...
Trigent Software - Professional ServicesMeerut
Required Skills
• Strong SAS programming expertise; Minimum 1 Year of R programming.
• Hands-on experience with SDTM, ADaM, TLFs, and regulatory submissions.
• Good understanding of CDISC standards and clinical trial processes....
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