Roles and Responsibilities Your primary responsibility will be to integrate with the existing laboratory workflow and maintain good (a) Identifying patients eligible for the study (b) Check availability of samples from biobank (c) Isolation and Quality Control of DNA and RNA required for the RADICAL workflow (d) Active participation in library preparation and optimisation of the high-throughput workflows that (e) Proper documentation of regular experiments carried out and troubleshooting if required. (f) Participation in SOP preparation and helping out with preparation of annual reports. (g) Basic data analysis skills Minimum required qualifications/experience (ICMR Guidelines) 1. Three Years Graduate in relevant subject/field + three years experience Post-Graduate in relevant subject/field 2. For Engineering/IT/CS- First Class Four Years Graduate Degree + Three Years Experience. Desired qualifications/experience (a) M.Sc. (with 1-2 years of experience) in Biological Sciences with expertise in Molecular Biology and (b) Expertise in DNA extraction, qPCR, Sanger Sequencing, NGS library preparation and sequencing using (c) Soft skills: MS Office, Excel, Laboratory and clinical data documentation, Data analysis tools using R packages, PRISM, SPSS etc. (preferable) (a) Integrity, motivation, enthusiasm, responsibility and reliability (b) Focus and commitment in carrying out tasks and duties (c) Critical analytical and problem-solving skills, capable of independent work (d) Ability to work effectively as part of a multidisciplinary team Knowledge/ Aptitude/Skills, Requirements Essential / desirable a. Integrity b. Flexibility c. Motivated d. Committed e. Willing to learn new skills f. Works as part of a team g. Receptive to new ideas h. Capable of independent work & to an agreed plan i. Good time management j. Organized, able to prioritize responsibilities k. Works to high technical and Essential i. Essential 2. Education / Qualifications M.Sc. in Biological Science (1-4 yrs experience) 3. Experience a. Good laboratory practice b. DNA and RNA technology c. Library preparation for sequencing d. Handling Illumina sequencer a. Essential b. Essential c. Desirable d. Desirable Application form CV Interview & References 4. Skills and ability a. Critical thinking b. Problem solving skills c. Readiness to evaluate, develop and test new approaches and strategies d. Mentoring junior team members a. Essential b. Essential c. Essential d. Desirable

DHR-ICMR Advanced Molecular Oncology Diagnostic Services (DIAMOnDS) PROJECT Conceptualised in the year 2004 as a philanthropic initiative for the Eastern and North- Eastern parts of India and the neighbouring countries, the Tata Medical Centre (TMC) started operations in Kolkata on May 16, 2011. The hospital is governed by a charitable trust Tata Medical Centre Trust. It is an integrated Oncology facility with well-trained professional staff and equipped with modern facilities and the most contemporary medical equipment. Set up at a cost of more than 500 crores, the Hospital, with a capacity of 450 beds, serves all sections of the society, with a proportion of the infrastructure earmarked for free/subsidized treatment for the underprivileged sections. The hospital provides a wide spectrum of services from diagnosis, therapy to rehabilitation and palliative support in cancer. The Institutions objective is to excel in service, education and research. TMC invites applications for the following positions under DHR-ICMR Advanced Molecular Oncology Diagnostic Services (DIAMOnDS) proposal to set up zonal Immuno- Histochemistry, Cytogenetics and Molecular Pathology labs to provide basic as well as high-end advance diagnostic services to cancer patients and research facilities for basic, translational and clinical research (https://dhr.gov.in/node/1533). DHR-ICMR Advanced Molecular Oncology Diagnostic Services (DIAMOnDS) Funding Agency: DHR-ICMR Qualification: - B.Sc in any science subject / B.C.A. Experience: Fresher. 2 to 3 years experience in computers and data management is desirable. Duration of the Employment: One years from the date of appointment, extendable yearly; maximum upto three years. Selected candidate will have to join at the earliest. The Project is likely to continue for three years with yearly extensions. Job Description: The candidate should be able to design and develop a data base for lung and breast cancer. Should be involved in data collecting, data entry, evaluating and drafting reports concerning data findings. Able to deal with data protection, different queries and implement quality control procedures and guidelines. Enter & update patient demographics, diagnosis, treatment & follow up information in the DIAMOnDS database. Maintain & manage electronic and paper based medical records related to the cancer care. Co-ordinate with OPD on regular basis for registering the patient s in the project as per the guideline. Co-ordinate with outside hospitals, receive the samples with proper labeling and upload it in database. Generate data report and submit it to the NCDIR as required. Follow standard operating procedures (SOPs) for data entry & data quality control. *For more details and application forms, please log on to our website today: www.tmckolkata.com. Last date of receiving application: 20/6/2025 You may also Email or Post applications to : Mr. Suvasish Mukherjee, Head- Human Resources, Tata Medical Center, 14 MAR (EW), New Town, Kolkata 700156.

Primary Responsibilities: Develop and refine study designs to ensure scientific rigor and alignment with research objectives. Analyse data according to study statistical plan tailored to the studys specific needs, ensuring that data collection methods align with intended analysis strategies. Compile comprehensive reports for relevant committees and funding agency, that summarize the study progress, challenges encountered, and future directions. Organize project meetings to manage progress and timelines. Preparing manuscripts for scientific communication. Site monitoring visits and audits: manage the monitoring visits and address any deviations or concerns related to study execution. Execute action points as indicated by the study monitor during the visit and generate closure reports. Data Audits: Perform thorough audits of collected data to verify accuracy, completeness, and adherence to the study design and ethical standards. Team Collaboration: Work closely with a multidisciplinary team, including data managers, statisticians, other researchers, and clinical staff, to ensure that all aspects of the study are Minimum Essential Qualifications: First Class Post Graduate Degree, including the integrated PG degrees, with PhD Second Class Post Graduate Degree, including the integrated PG degrees, with PhD and with For Engineering/IT/CS- First Class Graduate Degree of four years with three years experience Desirable Qualifications/experience: Experience in clinical or health services research, including expertise in study design and research methodology. Experience in conducting/managing operational feasibility studies Minimum 3 years of experience in clinical data analysis, statistical analysis of large datasets, or Experience in statistical methods, exploratory data analysis, multivariate data analysis, linear, logistic, Poission regression with diagnostic checking, survival analysis, and their implementation in R, SAS, Graphpad prism, or other statistical software. Excellent written and oral communication skills, capable of effectively presenting research findings and writing complex reports. Demonstrated ability to lead and manage research projects, including coordination of Knowledge of regulatory standards and ethical guidelines pertinent to clinical research. Strong attention to detail and commitment to accuracy. Good organizational skills and ability to manage multiple tasks.

The Project Research Scientist II (Non-Medical) plays a crucial role in shaping the direction and success of clinical and health services research projects. This position requires expertise in scientific research, good organizational skills, and the ability to navigate complex regulatory environments. Primary Responsibilities: Develop and refine study designs to ensure scientific rigor and alignment with research objectives. Analyse data according to study statistical plan tailored to the studys specific needs, ensuring that data collection methods align with intended analysis strategies. Compile comprehensive reports for relevant committees and funding agency, that summarize the study progress, challenges encountered, and future directions. Organize project meetings to manage progress and timelines Preparing manuscripts for scientific communication. Site Audits: Conduct regular site visits to ensure compliance with study protocols and Good Clinical Practice (GCP) guidelines. Address any deviations or concerns related to study execution. Data Audits: Perform thorough audits of collected data to verify accuracy, completeness, and adherence to the study design and ethical standards. Team Collaboration: Work closely with a multidisciplinary team, including data managers, statisticians, other researchers, and clinical staff, to ensure that all aspects of the study are Minimum required qualifications/experience: First class post-graduate degree, including integrated PG degrees, with three years experience or Desirable: Experience in clinical or health services research, including expertise in study design and research methodology. Experience in conducting/managing operational feasibility studies Excellent written and oral communication skills, capable of effectively presenting research findings and writing complex reports. Demonstrated ability to lead and manage research projects, including coordination of Knowledge of regulatory standards and ethical guidelines pertinent to clinical research. Strong attention to detail and commitment to accuracy. Good organizational skills and ability to manage multiple tasks.