Latest Job Openings
Showing 6 of 120+ opportunities
Conduct clinical trials, site monitoring, data collection and ensure compliance with GCP.
Develop & validate SAS programs, datasets and outputs for clinical research studies.
Analyze biological data, perform sequence analysis and generate meaningful insights.
Evaluate adverse events reports, documentation, and maintain regulatory safety reporting.
Coordinate dossier submissions, CTD compliance, and liaise with healthcare regulatory authorities.
Oversee EDC databases, perform data cleaning and validation according to clinical protocols.
Lead multi-center clinical trials, conduct site visits, and ensure strict ICH-GCP protocol adherence.
Generate CDISC SDTM/ADaM datasets, TLFs and validation programs for global regulatory submissions.
Perform safety surveillance, ICSR case processing, signal detection and aggregate safety reporting.
Develop automated NGS pipelines, sequence annotation workflows and clinical genomics data models.
Oversee USFDA and EMA dossier submissions, variation management, and regulatory compliance.
Author Clinical Study Reports (CSR), protocols, investigator brochures, and safety narratives.
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FAQs on Cliniwave Job Portal
New career opportunities across Clinical Research, Clinical SAS, Bioinformatics, and Pharmacovigilance are updated on our job portal regularly on a daily and weekly basis in partnership with leading CROs, pharmaceutical MNCs, and healthcare organizations across India and globally.
Yes! The Cliniwave job portal features dedicated entry-level and fresher job openings (0-1 year experience) alongside mid-level and senior roles. Look for the 0-2 Years and Fresher badges on job listings to explore entry-level positions.
While the job portal is open for all healthcare and life science graduates to explore, Cliniwave certified students receive priority placement assistance, direct interview referrals, resume boosting, and mock interview preparation with hiring partners.
Simply click on the Apply Now button on any active job card. You will be guided to submit your resume, portfolio, and credentials directly to the hiring company or through Cliniwave's placement desk.
We host openings for Clinical Research Associates (CRA), Clinical SAS Programmers, Bioinformatics Analysts, Drug Safety Associates (Pharmacovigilance), Regulatory Affairs Executives, Clinical Data Managers (CDM), and Medical Writers across top healthcare hubs including Bangalore, Hyderabad, Pune, Mumbai, Delhi NCR, and Remote.
Yes! You can use the Location filter on the portal to select Remote or Hybrid to discover flexible work-from-home opportunities in Clinical SAS programming, Medical Coding, and Bioinformatics data analysis.
Cliniwave provides 100% dedicated placement support, including 1-on-1 mentorship, GCP/ICH compliant project portfolios, SAS coding validation, resume building, and direct campus recruitment drives with 100+ hiring partners like IQVIA, Novartis, Pfizer, Parexel, and ICON.