Kg Puneeth Kumar
M Pharm
- Role
- Clinical Process Coordinator at IQVIA
- Location
- Bengaluru, KA, IN
- LinkedIn followers
- 500 followers
About Kg Puneeth Kumar
Clinical Research professional with hands-on experience as a Clinical Process Coordinator (CTA) at IQVIA, contributed to 3 global clinical trials in the diabetes therapeutic areaduring study start-up phase and close-out phase. At IQVIA, coordinated essential documentation across 150+ global clinical sites, maintained eTMF quality through document tracking, milestone reconciliation, and follow-ups with site teams. I supported Clinical Research Associates (CRAs), Clinical Leads, and Study Managers by managing CTMS entries, conducting quality checks of site and PI data, maintaining training logs, providing system access (CDMS, Preclarus etc.), and ensuring study systems remained compliant and current. My responsibilities extended to filing and organizing critical study documents (e.g, SDVs, DOAs, SIVs, COVs, IP logs, CRA meeting materials, SVRs, MVRs, study team member transitions checklists) and tracking milestone triggers to ensure timely updates and TMF completeness. Due to personal circumstances, I concluded my role on 4 June 2025 to prioritize personal responsibilities, and have since focused on strengthening my knowledge in Clinical Research, Data Management, Pharmacovigilance, and Regulatory Affairs through upskilling. I’m now seeking new opportunities to apply my knowledge, experience, skills and continue learning in a collaborative environment. Open to entry-level roles or those aligned with my background. Looking forward to the opportunity to restart my career. I bring a commitment to compliance, detail orientated and cross-functional teamwork. Available immediately | Reach out to me at p••••••••@gmail.com
Experience
Clinical Process Coordinator
Jan 2025 — Present · Bengaluru, IN
Contributed to global clinical trials in the diabetes therapeutic area during study start-up phase and the close-out phase. Collaborated with cross-functional teams across 150+ global sites to ensure timely documentation, compliance, and operational support.Key Responsibilities & Contributions:Study Start-up Support:Assisted the SGTM in creating study-specific and project-specific folders.Conducted initial quality checks during PI addition to CTMS.Supported access management for study team members (CRA, SRS, etc.) in platforms such as CDMS and Preclarus.Handled project training coordination, including compliance tracking and eTraining updates.Ongoing Study Activities:Ensured accurate and timely updates of clinical systems and maintained compliance with monitoring plans.Supported CRA, SGTM, and cCRA with transition documentation checklists and filing.Assisted in the periodic review of study files for accuracy, completeness, and audit readiness.Close-out Phase Tasks:Conducted eTMF review and filing of essential documents: SDVs, DOAs, In-Progress PD logs, IP logs, and related site documentation.Performed milestone trigger checks (e.g, Pre-FPV) and ensured corresponding documents were filed correctly.Tracked document status with CRAs and ensured timely follow-up for any pending items.Team Collaboration & Contribution:Maintained effective communication with internal stakeholders to meet project timelines.Proactively supported team members in additional responsibilities, demonstrating adaptability and ownership.
Education
SCS college of Pharmacy Hospet
Bachelor of Pharmacy - B. Pharm
2018 — 2022
Rajiv Gandhi University of Health Sciences
Master's of Pharmacy
2023 — 2024
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