837 Madurai Kamaraj University jobs in India

Responsibilities

Core responsibility related to GLP Study Director

• Approve the study plan and any amendments to the study plan by dated signature.
• Make the study plan available to RQA for verifying that it contains all information required for compliance with the GLP Principles.
• Ensure that the RQA have a copy of the study plan and any amendments in a timely manner and communicate effectively with the RQA as required during the conduct of the study.
• Ensure that study plans, amendments (if any) and Standard Operating Procedures are available to study personnel during conduct of study.
• Ensure that the final study plan and report for a multi-site study identify and define the role of any Principal Investigator(s) and test facility including test sites involved in the conduct of the study.
• Ensure that the procedures specified in the study plan are followed, and document the impact of any deviations from the study plan on the quality and integrity of the study, and take appropriate corrective action if necessary; acknowledge deviations from SOPs during the conduct of the study.
• Ensure that all raw data generated are fully documented and recorded.
• Ensure that computerized systems used in the study have been validated.
• Sign and date the final report to indicate acceptance of responsibility for the validity of the data and to indicate the extent to which the study complies with Principles of GLP.
• Ensure that after completion (including termination) of the study; the study plan, the final report, raw data and supporting materials are archived.
• Standardisation/validation of new toxicity study - Administrative: Requesting and coordinating resources provided by Management
• Personnel, Equipment and Facilities to ensure they are adequate and available as scheduled for the proper conduct of the study. Allied responsibility:
• Co-ordination with IAEC members.
• General material procurement.
• To help in facility maintenance.
• Communication with finance team, purchase team and suppliers.
• Communication with sponsor’s, if specified in study allotment letter. Any additional responsibility / activity as and when assigned by management which would not arise any conflict of interest.
• Conducting various Pre-Clinical efficacy studies
• Record maintenance related to Pre-Clinical efficacy study
• Development of various animal models and its standardization/ validation

Qualifications

• MSc (Zoology)/ M. pharma (Pharmacology)/MVSC
• 5 - 10 years of work experience
• Proficient in Microsoft Office
• Strong work ethic and passion for the research subject
• Strong communication, analytical and critical thinking skills

Find your next role with MedGenome Labs Ltd. We are the market leader in clinical genomic space in India and offers a comprehensive rangeof diagnostic servicesto doctors and researchers. We operate the largest CAP accredited Next Generation Sequencing (NGS) lab in Southeast Asia housing cutting-edge genome sequencing platforms. MedGenome is the founding member of GenomeAsia 100K, an initiative to sequence 100,000 Genomes in Asia.

We have an exciting opportunity for the position of Research Associate in New Delhi location. It is a full time and work from office opportunity.

Skills and Experience Required:

• 2+ years of experience in Extraction of nucleic acids (DNA/RNA) from biological materials including prenatal samples
• Performing QC for nucleic acids
• Processing samples for fragment analysis based tests – MCC and Aneuploidy (QF-PCR) & repeat nucleotide disorders.
• Processing samples for Sanger (Single variant & Prenatal) and MLPA based tests.
• Analysis, interpretation and reporting for MCC, QF-PCR, Sanger & MLPA data.
• Processing samples for NGS libraries and sequencing.
• Updating LIMS & MIS properly to ensure seamless workflow.
• Maintaining inventory while giving timely updates and ensuring the lab is in order
• Ensuring documentation of worksheets and methodical filling of all log sheets which include instrument log sheets and process related google sheets.
• Coordinating with the managers for sample processing, QC checks, documentations and maintaining turnaround time in each step of the process
• Taking part in CAP and other accreditation affairs. Follow CAP related activities and CAP compliance in the workplace
• Strictly adhere to lab Quality Processes and follow Standard Operating Procedures (SOPs)
• Training new joiners in Standard Operating Procedures (SOPs) and lab workflows
• Maintain cordial working relationship with everyone in the company
• Test optimization where required and any other responsibilities assigned by the Manager/Company.
• Maintaining a cordial working relationship with everyone in the company

Educational Qualification:

Masters in Human Genetics or Biotechnology or relevant studies.

If you are interested in this position, please click the APPLY NOW button for immediate employment consideration. We regret that due to volume of response, we can only contact initial successful applicants. If you have not heard from us within 7 days, then your application has been unsuccessful.

About the Role:

We are seeking a Research Associate to play a key role in advancing our work at the intersection of finance and technology. The role involves conducting financial, market, and regulatory research, while also developing decision frameworks and analytical models that inform investment evaluation and strategy. This is a rare opportunity for young professionals to combine financial expertise with emerging technology tools, and to go beyond research by shaping actionable insights that drive decision-making in a fast-growing environment.

Key Responsibilities:

• Investment Research & Tracking: Monitor equity and other financial products, track performance, and identify emerging opportunities and risks.

• Analytical Frameworks: Contribute to the development of decision flows and models that support systematic investment evaluation and scenario analysis.

• Regulatory & Policy Tracking: Monitor updates from regulators (RBI, SEBI, IRDAI, etc.) and assess their implications.

• Insight Generation: Collect and synthesize data into concise briefs, reports, models, and presentations. Translate findings into structured recommendations.

• Collaboration: Work with product, strategy, and technology colleagues to ensure research inputs shape practical solutions. 

Requirements:

Education: 

• Bachelor’s degree in Economics/Finance/Management/Public Policy/Computer Science.

• Postgraduate degree (MBA/Finance/Economics) or professional qualifications (CA, CFA, FRM) are a plus.

Experience:

• 2-4 years of experience in equity markets, investment research, consulting, or financial analysis.

• Broader exposure to mutual funds, fixed income or alternative investments, or professional backgrounds such as CA/CPA is a plus.

• Familiarity with technology-enabled research and analysis (advanced Excel/Sheets, familiarity with AI-tools required; SQL/Python/R or financial databases a plus).

Skills & Competencies:

• Strong understanding of financial statements, valuation, and market structures.

• Proficiency in financial modelling and quantitative/qualitative research.

• Experience designing structured analytical approaches and decision frameworks.

• Clear, concise communication skills; ability to present insights to diverse stakeholders

Why this role?

• Go beyond research: Shape decision frameworks and models that directly influence strategic outcomes.

• Finance + Tech exposure: Build on your equity markets expertise while expanding into a wide spectrum of financial products and technology-driven analysis.

• High-growth environment: Work closely with leadership, take on early responsibility, and grow your career in an ambitious, impact-driven setting.

If you're excited about this opportunity, send your resume to

Responsibilities

Core responsibility related to GLP Study Director

• Approve the study plan and any amendments to the study plan by dated signature.
• Make the study plan available to RQA for verifying that it contains all information required for compliance with the GLP Principles.
• Ensure that the RQA have a copy of the study plan and any amendments in a timely manner and communicate effectively with the RQA as required during the conduct of the study.
• Ensure that study plans, amendments (if any) and Standard Operating Procedures are available to study personnel during conduct of study.
• Ensure that the final study plan and report for a multi-site study identify and define the role of any Principal Investigator(s) and test facility including test sites involved in the conduct of the study.
• Ensure that the procedures specified in the study plan are followed, and document the impact of any deviations from the study plan on the quality and integrity of the study, and take appropriate corrective action if necessary; acknowledge deviations from SOPs during the conduct of the study.
• Ensure that all raw data generated are fully documented and recorded.
• Ensure that computerized systems used in the study have been validated.
• Sign and date the final report to indicate acceptance of responsibility for the validity of the data and to indicate the extent to which the study complies with Principles of GLP.
• Ensure that after completion (including termination) of the study; the study plan, the final report, raw data and supporting materials are archived.
• Standardisation/validation of new toxicity study - Administrative: Requesting and coordinating resources provided by Management
• Personnel, Equipment and Facilities to ensure they are adequate and available as scheduled for the proper conduct of the study. Allied responsibility:
• Co-ordination with IAEC members.
• General material procurement.
• To help in facility maintenance.
• Communication with finance team, purchase team and suppliers.
• Communication with sponsor’s, if specified in study allotment letter. Any additional responsibility / activity as and when assigned by management which would not arise any conflict of interest.
• Conducting various Pre-Clinical efficacy studies
• Record maintenance related to Pre-Clinical efficacy study
• Development of various animal models and its standardization/ validation

Qualifications

• MSc (Zoology)/ M. pharma (Pharmacology)/MVSC
• 5 - 10 years of work experience
• Proficient in Microsoft Office
• Strong work ethic and passion for the research subject
• Strong communication, analytical and critical thinking skills