Manages pharmaceutical tender submissions for central and state government hospitals. Monitors tender notifications from GeM, eProcure, and state procurement portals. Prepares tender documentation including technical and commercial bid documents. Coordinates product qualification and registration for government tender participation. Manages rate contract renewals and existing government supply agreements. Coordinates with supply chain for tender price calculations and availability. Builds relationships with government procurement officers and hospital administrators. Tracks tender outcomes and prepares business analysis for management review. Manages government account receivables and coordinates payment collections. Coordinates with regulatory affairs for product approvals required for tenders. Prepares quarterly government business reports and forecasts for management. Supports PMBJP and Jan Aushadhi scheme registration and supply activities. Stays current with GeM portal updates, DPCO pricing, and government procurement policies.

Prepares high-quality clinical study reports for Phase I to III clinical trials. Writes clinical sections of regulatory submissions including CTD modules 2 and 5. Drafts investigator brochures, informed consent forms, and patient information sheets. Prepares scientific manuscripts and posters for publication in medical journals. Writes PBRER, DSUR, and periodic safety update reports for regulatory submissions. Develops standard operating procedures and training materials for clinical teams. Reviews and edits documents prepared by investigators and study teams. Coordinates with clinical, regulatory, and medical affairs teams for document review. Manages document versions and tracks review cycles through electronic systems. Ensures all documents comply with ICH, CONSORT, and regulatory style guides. Supports preparation of responses to regulatory authority queries on documents. Maintains awareness of recent clinical data for therapy area writing activities. Stays current with ICH E3, E8, publishing software, and medical writing standards.

Creates accurate and high-quality scientific and medical content. Writes clinical study reports, protocols, and regulatory submissions. Develops manuscripts for peer-reviewed scientific journals. Prepares medical education materials, CME content, and training modules. Writes product monographs, prescribing information, and label text. Creates patient-facing health information in clear language. Collaborates with medical affairs, clinical, and regulatory teams. Ensures all content complies with CONSORT, ICH E3, and editorial guidelines. Reviews and edits medical content for accuracy and clarity. Manages multiple writing projects to agreed timelines and quality standards. Participates in author and KOL liaison for publications. Stays current with therapeutic area literature and scientific advances. Prepares bibliographic summaries and evidence-based literature reviews.

Performs elective and emergency general surgical procedures daily. Manages appendicitis, hernias, gallbladder disease, and bowel conditions. Performs laparoscopic and open abdominal surgical techniques. Conducts pre-operative evaluation and post-operative patient care. Manages surgical complications and coordinates ICU care. Participates in MDT discussions for complex surgical cases. Supervises surgical residents and medical students in theatre. Ensures sterile technique and patient safety in the OR. Reviews imaging and pathology to plan surgical interventions. Performs endoscopic procedures including gastroscopy and colonoscopy. Contributes to surgical audit and quality improvement programs. Stays current with surgical guidelines and evidence-based practice. Manages emergency on-call duties and trauma cases.

Position: Clinical Data Manager We invite a proactive and capable Clinical Data Manager to lead and execute within a collaborative, agile environment. The incumbent will operate in a structured yet agile environment that prioritises quality and professional growth. Scope of Responsibilities: Maintain up-to-date knowledge of ICH E2A-E2F, GCP, and pharmacovigilance regulations. Ensure all cases are coded and processed per MedDRA and applicable global standards. Participate in regulatory inspections, health authority meetings, and internal audits. Conduct structured literature reviews and contribute to scientific summaries and labelling. Prepare high-quality clinical and regulatory documents aligned to CTD submission standards. Liaise with clinical, medical affairs, and regulatory teams for accurate safety data management. Assist in preparing and submitting regulatory safety reports in compliance with ICH guidelines. Review and analyse PSURs, PBRERs, DSURs, and other aggregate safety reports. Competencies and Qualifications: Commitment to ongoing professional learning and industry knowledge enhancement. Exceptional organisational skills with the ability to handle multiple concurrent responsibilities. Ability to work both independently and in a team-oriented, collaborative environment. Detail-oriented mindset with the ability to synthesise and present complex information clearly. At least 24 years of hands-on experience in a comparable professional setting. Bachelor's degree in a relevant discipline; master's degree or professional certification is preferred. Knowledge of ICH E2A-E2F, MedDRA coding, GCP, and global regulatory requirements. This is an outstanding opportunity for a motivated professional to advance their career within a reputable organisation.