We are seeking a dedicated Clinical Research Coordinator to join our growing clinical team. The CRC will support the planning, coordination, and execution of clinical trials according to regulatory guidelines and Good Clinical Practice standards.
Responsibilities: Assign accurate medical codes (ICD-10, CPT) based on patient records Understand basic anatomy, physiology, and medical terminology Follow guidelines from CMS, AAPC, and internal policies Work under the supervision of senior coders or team leads Maintain productivity and accuracy benchmarks
Clinical Data Associate ensures accurate management and validation of clinical trial data. Responsibilities include data entry, query resolution, reconciliation, and supporting the team to maintain compliance with GCP standards throughout the trial.
We are seeking a motivated and detail-oriented Entry-Level Clinical Research Associate to join our team.This role is ideal for recent graduates or freshers with a background in life sciences or pharmacy, looking to build a career in clinical research
As a Clinical Research Coordinator (CRC), you will assist in the planning, coordination, and execution of clinical trials at the site level. Required Candidate profile Assist the Principal Investigator in screening, recruiting, and enrolling study participants. Schedule subject visits and coordinate study-related procedures.
We are looking for Entry-Level Medical Coders who are passionate about healthcare and eager to begin a career in medical coding. Fresh graduates with relevant education or certification are welcome to apply. Required Candidate profile As a Medical Coder, you will be responsible for reviewing clinical documents and assigning appropriate medical codes for diagnoses, procedures, and services.
Entry-level Pharmacovigilance Associate responsible for processing adverse event reports, data entry, MedDRA coding, narrative writing, and ensuring regulatory compliance. Supports safety reporting for clinical and post-marketing activities.
Regulatory documentation, CTD/eCTD dossier preparation, product registration, license renewal, CDSCO guideline knowledge, and coordination with QA/QC/Production. Freshers welcome. Hybrid work mode.
Entry-level Pharmacovigilance Associate responsible for processing adverse event reports, data entry, MedDRA coding, narrative writing, and ensuring regulatory compliance. Supports safety reporting for clinical and post-marketing activities.