Open to opportunities

Dr Aamuktha Pvnls

@draamukthapvnls

India

Message

What I'm looking for

I’m looking for a GCP-forward clinical trials role where I can drive audit-ready TMF/eCRF documentation, strong quality checks, and cross-site coordination—available immediately for remote, hybrid, or on-site opportunities globally.

I am a medically qualified Clinical Trial Associate (BHMS) from Hyderabad, India, with ICH-GCP E6 R3 certification (2026) and a Johns Hopkins Clinical Trials Specialization (Coursera, 2026). I bring 2+ years of GCP-aligned research experience with CCRH, Govt. of India, hands-on familiarity with Veeva Vault (eTMF), Medidata Rave, CTMS, and REDCap workflows, and a strong background in study start-up, audit-ready documentation, and site coordination. I am available immediately for remote CTA, CRC, TMF Specialist, Medical Writer, or Pharmacovigilance roles globally.

Experience

Work history, roles, and key accomplishments

Current

Founder & Consulting Clinician

Current

Vaidya Setu Homoeo Clinic

Sep 2025 - Present (8 months)

Built a GCP-aligned documentation system generating 20–25 audit-ready case records weekly with near-zero inconsistency rates. Produced 100+ structured clinical outcome reports and authored 15+ patient education documents, standardizing templates to improve inspection readiness and traceability.

Clinical Documentation Clinical Data Management Medical Writing

Duty Medical Officer

Srikara Hospitals

Jul 2025 - Aug 2025 (1 month)

Maintained 100% documentation compliance across 30–40 daily OPD and emergency cases with zero reported errors. Matched real-time EMR entries to CRF completion standards and coordinated multi-department patient handovers while producing structured discharge summaries under time pressure.

Trial Style Documentation

Research Contributor

Central Council for Research in Homoeopathy

Jan 2023 - Apr 2025 (2 years 3 months)

Delivered 2+ years of GCP-aligned support for a nationally funded government research study, including audit-trail maintenance and protocol-aligned documentation. Contributed to study start-up filing into master-file systems, conducted PubMed literature synthesis, and performed QA/data consistency checks on collected records.

PubMed Clinical QA Checks