Clinical Trials Jobs in Thāne
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Search Results - Clinical Trials Jobs in Thāne
ProductLife GroupThāne
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 RecruitingThāne
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, ideally gained...
Safeguard Global RecruitingThāne
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...
Safeguard Global RecruitingThāne
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...
ClinoGenesis Research InstituteThāne
and data integrity.
• Collaboration: Working closely with our senior team to support clinical trial operations and study coordination.
• Reporting: Learning the basics of tracking trial progress and ensuring all data is audit-ready.
What We Are Looking...
VeramedThāne
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...
Teamware SolutionsThāne
/ statistical programming experience within pharmaceutical clinical development - Supporting regulatory filings (e.g. NDA, BLA, MAA)
• Knowledge of the drug development process, clinical trial methodology, statistics and familiarity with global regulatory...
ACL DigitalThāne
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...
CytelThāne
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...
Statistical InsightsThānemncjobsindia.com
As a pharmacologist you ll need to design plan and conduct controlled experiments and or clinical trials to improve understanding of a drug s activity collect analyse and interpret data using computers high technology measuring systems...
VeramedThāne
knowledge 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...
IqviaThānefoundit.in
of internal systems, databases, tracking tools and project plans.; - Manage the operational insight of the assigned sites/studies and complete the study/site metrics trending (trend analysis of clinical aspects of the trial, share trends and agree on action...
IQVIAThānemncjobsindia.com
and Home Page Complete the Study Authorization Form and Trial Capacity Request Form InForm Attend the Pre-Design Meeting Online Screen Review Meeting Unblinded Data review meeting Attend and present comments at the Internal Design Review Meeting May...
CytelThāne
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...
IQVIAThānemncjobsindia.com
support as appropriate If applicable may be accountable for supporting development of project subject recruitment plan on a per site basis If applicable may be accountable for site financial management according to executed clinical trial agreement...
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