Datar Cancer Genetics Limited
Website:
datarpgx.com
Job details:
Company Description Datar Cancer Genetics Limited is a world-leading molecular oncology facility that combines fully equipped laboratories, integrated process platforms, and an in-house bioinformatics team to deliver precise, up-to-date reporting. The organization is NABL, ISO, CAP, and CLIA accredited, and serves national and international cancer research institutes as well as patients from regions including the US, Switzerland, Germany, and the UK. Leveraging the latest technology and many years of extensive research, Datar Cancer Genetics provides advanced treatment options for patients whose cancer has not responded to multiple lines of therapy. The state-of-the-art cancer research center spans 40,000 sq. ft. and is staffed by a diverse team of researchers, doctors, scientists, and technologists trained at leading global institutions. The team collaborates closely with clinicians and patients to deliver cutting-edge solutions for complex and challenging cancer cases.
Role Description This is a full-time, on-site role based in Bengaluru. The Job Title will contribute to ongoing oncology research and clinical applications by supporting laboratory workflows, collaborating with multidisciplinary teams, and adhering to established quality and safety standards. Day-to-day responsibilities may include collecting, organizing, and analyzing data; preparing accurate documentation and reports; and assisting in the implementation and optimization of diagnostic or treatment-related processes. The role involves regular interaction with scientists, clinicians, and technical staff to ensure that project milestones are met and that outcomes align with regulatory and institutional guidelines. The Job Title is expected to maintain a high level of professionalism, continuous learning, and commitment to improving patient care.
Qualifications
- Strong foundation in life sciences, biotechnology, molecular biology, bioinformatics, or a related field; relevant degree or certification preferred.
- Experience working in a clinical, research, or laboratory setting with familiarity in standard lab procedures, documentation, and quality control.
- Ability to collect, interpret, and present scientific or clinical data accurately using basic analytical tools and software.
- Effective communication and collaboration skills to work with multidisciplinary teams, including clinicians, researchers, and technical staff.
- Attention to detail, strong organizational abilities, and a commitment to following regulatory, safety, and ethical guidelines.
- Adaptability to a fast-paced environment and willingness to learn and apply new technologies and methods in oncology.
- Prior experience in oncology, genetics, or precision medicine, and familiarity with accredited laboratory standards (NABL, ISO, CAP, CLIA) will be an advantage.
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