Their responsibilities include reviewing safety data, identifying potential safety signals, assessing causality, and providing guidance on risk management and communication. Key Responsibilities: Safety Data Review and Analysis Risk Management and Communication Regulatory Compliance Qualifications Bachelor's or Masters degree in a related field, such as Medicine, pharmacy or related field 0-2 years of experience in related field Strong analytical and problem-solving skills Excellent communication and interpersonal skills Ability to work independently and as part of a team Interested to apply can share CV or call/whatsapp to 9342735755

Responsibilities: Develop, configure, and maintain the SAS platform infrastructure across enterprise environments. Integrate SAS tools with external databases, applications, and data pipelines (e.g., Oracle, Hadoop, DB2, SQL Server). Design and implement SAS architecture, security, performance tuning , and automation solutions. Support the deployment, upgrade, and patching of SAS environments (e.g., SAS 9.4, SAS Viya). Work with application developers, data scientists, and administrators to ensure platform reliability and scalability. Manage SAS metadata, libraries, and user access controls . Troubleshoot system-level issues and optimize platform performance. Ensure compliance with IT policies, data governance, and audit requirements. Interested to apply can share CV or call/whatsapp to 9342735755

Roles and Responsibilities Lead global and local PV teams including medical reviewers, case processors, and safety scientists. Oversee ICSR management, medical assessments, signal detection , and aggregate report submissions (PSUR, PBRER, DSUR). Define and implement company-wide drug safety strategy aligned with regulatory expectations (CDSCO, EMA, FDA, MHRA, PMDA). Ensure full compliance with global PV regulations , including GVP Modules, ICH E2E/E2D , and local Indian guidelines. Liaise with Regulatory Affairs, Medical Affairs, Quality, Clinical, and R&D functions. Represent the company in regulatory inspections, audits , and safety governance boards . Review and sign-off on Risk Management Plans (RMPs) , Safety Data Exchange Agreements (SDEAs) , and PV SOPs . Guide implementation of PV systems and databases (e.g., Argus, ArisGlobal, Veeva Vault Safety). Lead PV input for due diligence, licensing, and product launches . Qualifications MBBS / MD / PharmD / PhD / MPharm / BDS (mandatory depending on regulatory scope) Additional certifications in GVP, ICH-GCP, Drug Safety, or PV Compliance are preferred Proven experience with regulatory authority interactions , inspections, and PV audits. Interested to apply can share CV or call/WhatsApp to 9342735755

Roles and Responsibilities: Analyze structured and unstructured data from EMR/EHR, clinical systems, pharmacy, claims , and public health databases Design dashboards and reports using Excel, Power BI, Tableau , or similar tools Use SQL / Python / R to retrieve, clean, and analyze large datasets Collaborate with clinicians, IT, and business teams to identify gaps and improve performance Perform trend analysis, predictive modeling , or cost-benefit studies on healthcare data Ensure data quality, privacy, and regulatory compliance (HIPAA / NABH / NDHM) Support population health management, disease tracking, or hospital operations Qualifications: Bachelors / Masters in Life Sciences, Statistics, Public Health, Computer Science, Pharmacy , or equivalent Certification in Health Analytics / Data Science / SQL / Power BI preferred Exposure to ICD-10, CPT, LOINC, SNOMED , or hospital data systems is a plus Interested to apply can share CV or call/whatsapp to 9384592766

Roles and Responsibilities; Provide scientific and clinical support to internal teams, field force, and external stakeholders. Develop and deliver medical education, scientific slide decks, advisory boards , and KOL engagement plans . Lead product monograph development , scientific publications , and medical content review . Collaborate with regulatory, R&D, pharmacovigilance, and marketing on product lifecycle. Participate in medical strategy development , ensure compliance with promotional practices. Ensure all materials meet global and local medical, ethical, and regulatory standards . Work with Medical Science Liaisons (MSLs) for field-based scientific engagement. Manage clinical studies (IIS/phase IV) in coordination with clinical operations teams. Eligibility / Qualifications: MBBS / MD / PharmD / Ph.D. / M.Pharm (Pharmacology / Clinical Pharmacy / Life Sciences) Knowledge of therapeutic areas, ICMJE, ICH-GCP, GVP , and Indian regulatory guidelines Strong experience in scientific writing, medical review, and stakeholder interaction Interested to apply can share you CV in Whatsapp/Call to 9342735755

Responsibilities: Write and optimize complex SQL queries, joins, subqueries, stored procedures, and triggers Extract, transform, and analyze data from multiple sources (relational databases, cloud platforms, APIs) Generate periodic and ad-hoc reports and dashboards for business stakeholders Work with cross-functional teams to translate business questions into data insights Perform data validation, profiling, and cleansing to ensure data accuracy and consistency Assist in database management tasks (indexing, tuning, monitoring performance) Document query logic, data dictionaries, and business rules Qualifications: Bachelors in Computer Science, Information Technology, Statistics, or related fields Certification in SQL (Oracle/MS SQL/MySQL/PostgreSQL) or BI tools (Power BI/Tableau) preferred Experience with ETL pipelines, data warehouses, or reporting tools is a plus Interested to apply can share CV or call/whatsapp to 9342735755

Responsibilities: Review CDM documentation for quality and compliance Ensure audit readiness of CDM systems and records Conduct internal data audits, QC checks , and issue CAPAs (Corrective & Preventive Actions) Track and report compliance metrics, deviations , and resolution timelines Coordinate with QA teams during sponsor or regulatory inspections Maintain version control and documentation logs for study-specific and global CDM SOPs Participate in training, process improvement , and standardization initiatives Ensure compliance with CDISC, SDTM , and eClinical tools standards. Interested to apply can share CV or call/whatsapp to 9342735755

The Clinical Safety Reviewer (CSR) is responsible for evaluating and interpreting adverse events (AEs), serious adverse events (SAEs), and product safety data collected during clinical trials or post-marketing surveillance. The role ensures scientific and regulatory accuracy in case assessments, contributing to patient safety and regulatory compliance. Roles and Responsibilities; Review clinical safety data including ICSRs, SAEs, and narratives for accuracy and medical completeness. Assess seriousness, expectedness, and causality based on protocol, IB, and regulatory guidelines. Ensure the consistency of MedDRA coding and WHO Drug coding in line with global standards. Review and approve final case versions for submission to regulatory authorities. Collaborate with medical writers, PV associates, and biostatisticians on aggregate report contributions. Participate in signal detection and risk assessment meetings (as required). Ensure compliance with global pharmacovigilance regulations (e.g., ICH E2E, GVP). Eligibility / Qualifications: MBBS / BDS / BPharm / PharmD / MPharm / BHMS / BAMS with relevant PV training. Minimum1- 4 years experience in pharmacovigilance or clinical safety (mandatory for mid-level). Strong understanding of clinical trial protocols, GCP, MedDRA, and WHO-DD. Hands-on experience with PV databases like Argus , ARISg , or equivalent. Interested to apply can share you CV in Whatsapp/Call to 9342735755

Roles & Responsibilities: Perform real-time and post-process data quality assessments across AI/ML models used in healthcare, clinical, or pharma systems. Identify data anomalies, bias, and drift in AI models to ensure reliable outcomes. Collaborate with data engineers, scientists, and medical teams to maintain compliance and accuracy of AI outputs. Design and implement AI model monitoring dashboards and alert systems. Define and document data validation rules, metrics (e.g., completeness, accuracy), and audit logs. Ensure compliance with industry standards in AI data usage. Participate in risk-based monitoring for clinical or pharmacovigilance systems. Report and correct system errors, inconsistencies, or validation failures in structured and unstructured data. Qualifications: B.Tech / M.Tech / B.Sc. / M.Sc. in Data Science, Computer Science, Bioinformatics, Statistics OR PharmD / B.Pharm / M.Pharm with AI/Data Analytics specialization or certification Certifications in AI in Healthcare or Regulatory Compliance preferred Interested to apply can share CV or call/WhatsApp to 9384592766

Roles and Responsibilities Prepare and review high-quality aggregate safety reports for regulatory submissions. Author and update Risk Management Plans, Core Safety Information, Company Core Data Sheets, and Safety Narratives. Collaborate with global cross-functional teams including pharmacovigilance, medical affairs, regulatory, clinical, and biostatistics. Interpret and summarize safety data from various sources including clinical trials, real-world evidence, and post-marketing surveillance. Track timelines and ensure timely delivery of all safety documents. Qualifications PharmD / M.Pharm / MBBS / BDS / MSc in Life Sciences or Pharmacology Certification in medical writing, regulatory affairs, or pharmacovigilance is an added advantage Strong analytical and problem-solving skills Excellent communication and interpersonal skills Ability to work independently and as part of a team Interested to apply can share CV or call/WhatsApp to 9342735755

Roles and Responsibilities; Perform medical review of ICSRs for seriousness, causality, and expectedness. Assess adverse events (AEs/SAEs) in clinical trial and post-marketing settings. Write and validate concise and medically accurate narratives . Conduct literature review and assist in signal detection & risk analysis . Support preparation of aggregate reports (PSUR, DSUR, PBRER). Collaborate with PV scientists, data entry teams, and global medical reviewers. Qualifications: MBBS / BDS / BAMS / BHMS / Pharm.D / M.Pharm (Pharmacology) 1-5 years of experience in Pharmacovigilance, preferably in medical review/assessment roles Interested to apply can share you CV in Whatsapp/Call to 9342735755

We are seeking an experienced Drug Safety Coding Specialist with a strong background in pharmacovigilance terminology and regulatory coding standards. Roles and Responsibilities Perform accurate and consistent coding of adverse events , medical history, lab terms, and concomitant medications using MedDRA and WHO-DD. Review and validate terms in Individual Case Safety Reports (ICSRs) to ensure alignment with global PV standards. Perform recoding or dictionary version updates in compliance with regulatory requirements. Collaborate with case processors, medical reviewers, and data management teams to resolve coding discrepancies. Ensure compliance with ICH-GCP , GVP , and internal SOPs. Maintain and update code lists and contribute to coding conventions development. Support training of new team members on dictionary use and coding best practices. Participate in audits, inspections , and quality control checks related to coding. Qualifications B.Pharm / M.Pharm / PharmD / MBBS / BDS / B.Sc. Life Sciences MedDRA coding training or pharmacovigilance certification is a plus Strong analytical and problem-solving skills Excellent communication and interpersonal skills Ability to work independently and as part of a team Interested to apply can share CV or call/WhatsApp to 9342735755

Roles and Responsibilities; Develop and review scientific content for clinical/scientific presentations, brochures, product monographs, patient education materials, slide decks, and white papers. Translate complex medical/scientific data into clear, engaging, and compliant communication for various audiences. Assist in the creation of publication plans, scientific abstracts, peer-reviewed articles, and regulatory documents. Collaborate with cross-functional teams including medical affairs, regulatory, pharmacovigilance, marketing, and clinical research. Ensure all content complies with company SOPs, regulatory standards, and industry codes. Conduct literature reviews, gap analysis, and content referencing from PubMed, Embase, Medline, etc. Attend medical conferences, KOL discussions, and advisory boards for content development and insight gathering. Qualifications & Experience: B.Pharm / M.Pharm / PharmD / MBBS / BDS / BAMS / MSc (Life Sciences, Biotechnology, Microbiology) Certification or diploma in medical writing or scientific communication (preferred) Interested to apply can share you CV in Whatsapp/Call to 9342735755