1,956 All India Institute Of Medical Sciences jobs in India

• Design and conduct advanced genomics experiments, including sample preparation for NGS.
• Perform library preparation, sequencing, and associated quality control measures.
• Analyze large-scale genomic datasets using bioinformatics tools and pipelines.
• Interpret sequencing data and troubleshoot experimental and analytical challenges.
• Collaborate with PIs and research staff on experimental design and data interpretation.
• Contribute to the writing of scientific manuscripts and grant proposals.
• Mentor and train junior research staff and students.
• Maintain accurate laboratory records and manage experimental data.
• Stay current with the latest advancements in genomics and bioinformatics.
• Contribute to the overall scientific strategy and direction of the research group.

• Ph.D. or Master's degree in Genomics, Molecular Biology, Bioinformatics, or a related life science field.
• Extensive hands-on experience with NGS library preparation techniques (e.g., Illumina, PacBio).
• Proficiency in using bioinformatics software, databases, and programming languages (e.g., R, Python) for data analysis.
• Demonstrated experience in analyzing various types of sequencing data (e.g., whole-genome, exome, RNA-seq).
• Strong understanding of genetic principles and molecular mechanisms.
• Excellent analytical, critical thinking, and problem-solving skills.
• Proven track record of scientific publications in peer-reviewed journals.
• Strong communication and interpersonal skills.
• Ability to work independently and collaboratively in a research team.

• Design and implement computational approaches to analyze large-scale biological datasets (genomics, proteomics, transcriptomics, etc.).
• Develop and validate novel algorithms and software tools for biological data analysis.
• Collaborate with experimental biologists, clinicians, and other researchers to define research questions and translate them into computational strategies.
• Interpret complex data, draw meaningful conclusions, and present findings to both technical and non-technical audiences.
• Contribute to the writing of research proposals, grant applications, and peer-reviewed publications.
• Stay current with the latest advancements in computational biology, bioinformatics, and related fields.
• Mentor junior researchers and provide technical guidance on computational methods.
• Manage research projects, ensuring timely completion and adherence to scientific rigor.
• Develop and maintain high-quality, well-documented code and workflows.
• Explore and implement cutting-edge machine learning and AI techniques for biological research.
• Contribute to the strategic direction of computational biology research within the organization.

• Ph.D. in Computational Biology, Bioinformatics, Computer Science, Statistics, or a related quantitative field.
• Minimum of 5 years of post-doctoral or industry research experience in computational biology or bioinformatics.
• Proven expertise in analyzing diverse biological datasets using statistical and computational methods.
• Strong programming skills in languages such as Python, R, or Perl.
• Experience with relevant bioinformatics tools and databases (e.g., BLAST, Gene Ontology, TCGA).
• Proficiency in machine learning techniques and their application to biological data.
• Excellent written and verbal communication skills, with a track record of publications.
• Ability to work independently, manage multiple projects, and collaborate effectively in a remote team.
• Strong analytical and problem-solving skills.
• Experience with high-performance computing environments is a plus.

• Design and develop clinical trial protocols in alignment with regulatory requirements and scientific objectives.
• Oversee the conduct of clinical trials, ensuring data integrity, patient safety, and protocol compliance.
• Select and qualify clinical trial sites and investigators.
• Monitor trial progress and manage timelines, budgets, and resources effectively.
• Analyze clinical trial data and interpret results to support regulatory submissions and product development.
• Prepare clinical study reports, manuscripts, and presentations for scientific and regulatory audiences.
• Collaborate with cross-functional teams, including R&D, regulatory affairs, and marketing.
• Stay current with scientific literature, emerging technologies, and regulatory changes in the pharmaceutical industry.
• Manage vendor relationships and ensure the quality of outsourced services.
• Contribute to the strategic planning of clinical development programs.

• PhD or Master's degree in Life Sciences, Pharmacy, Medicine, or a related field.
• 5-8 years of experience in clinical research within the pharmaceutical or biotechnology industry.
• In-depth knowledge of Good Clinical Practice (GCP), ICH guidelines, and regulatory affairs.
• Proven experience in designing and managing clinical trials across different phases.
• Strong understanding of statistical principles for clinical data analysis.
• Excellent scientific writing and presentation skills.
• Ability to work effectively in a cross-functional team environment.
• Strong analytical and problem-solving abilities.
• Proficiency in relevant software and data management systems.
• Adaptability to a hybrid work environment and strong organizational skills.

• Design and develop clinical trial protocols in alignment with scientific objectives and regulatory requirements.
• Oversee the execution of clinical trials, ensuring adherence to GCP and other relevant guidelines.
• Manage relationships with clinical sites, investigators, and study coordinators.
• Monitor study progress, data quality, and patient safety throughout the trial lifecycle.
• Analyze clinical trial data, interpret results, and contribute to the preparation of study reports.
• Collaborate with biostatisticians and data management teams to ensure data integrity.
• Prepare regulatory submissions, including Investigational New Drug (IND) applications and New Drug Applications (NDA).
• Contribute to the development of scientific publications and presentations.
• Stay abreast of the latest scientific advancements and regulatory changes in the pharmaceutical industry.
• Provide scientific and clinical expertise to internal teams and external partners.

• Ph.D. or M.D. in a relevant scientific discipline (e.g., Pharmacology, Medicine, Biology).
• Minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry.
• Proven track record in designing and executing Phase I, II, III, or IV clinical trials.
• In-depth knowledge of ICH-GCP guidelines and regulatory requirements (e.g., FDA, EMA, CDSCO).
• Strong understanding of drug development processes and biostatistics.
• Excellent scientific writing, presentation, and communication skills.
• Demonstrated ability to analyze complex scientific data and draw sound conclusions.
• Experience with clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to work collaboratively in a team environment and manage multiple projects effectively.
• Strong problem-solving skills and attention to detail.

Clinical Research Associate (Freshers Only)

Location : (Insert City or "Across India" if remote/hybrid)

Organization : Clinogenesis Research Organization

Department : Clinical operations

Type : Full-Time

About the Role:

Clinogenesis Research Organization is offering an excellent opportunity for fresh graduates to launch their careers as Clinical Research Associate.

Please note: This position is strictly for freshers. Candidates with prior experience are not eligible for this role.

If you’re passionate about clinical research and eager to grow in a structured, accredited environment, we invite you to apply.

Key Responsibilities:

• Assist with on-site coordination of clinical trial activities under supervision
• Maintain essential documents, site files, and case report forms
• Support the investigator in protocol compliance and patient coordination
• Ensure all trial activities adhere to ICH-GCP and ethical guidelines
• Participate in training sessions and team meetings as part of learning

Eligibility Criteria:

• Education: , B pharma , M pharma, B.Sc / M.Sc in Life Sciences, Pharmacy, Nursing, or equivalent healthcare field
• Experience: Freshers only
• Strong communication and organizational skills
• Eagerness to learn and grow in the clinical research domain

Why Start at Clinogenesis?

• Work alongside expert mentors and gain practical exposure
• Structured learning in a globally accredited research setup
• Continuous development and support for long-term career growth

Job Description

We are seeking a highly organized and proactive Clinical Research Assistant to support the daily operations of our longitudinal clinical trials. The study involves Continuous Glucose Monitoring (CGM), lab testing, gut microbiome analysis, and remote consultations with physicians. The ideal candidate will play a critical role in coordinating participant involvement, ensuring accurate data collection, and maintaining clear communication among all stakeholders including patients, labs, physicians, and the internal research team.

Key Responsibilities

Participant Coordination:

· Schedule and follow up on appointments for CGM setup, lab tests, stool sample collection, and virtual consultations.

· Provide clear instructions and support to participants for app usage and test procedures.

Data Collection & Management:

· Monitor and collect data from wearable CGM devices and study-related apps.

· Ensure timely entry and validation of participant data in study databases or CRFs (Case Report Forms).

· Flag and report data inconsistencies or protocol deviations to the study coordinator or PI.

Communication & Support:

· Act as a liaison between participants, clinical labs, logistics partners, and physicians.

· Maintain regular, empathetic communication with participants to encourage adherence and resolve concerns.

· Coordinate specimen shipment and tracking with third-party labs.

Documentation & Compliance:

· Maintain accurate participant records in accordance with GCP (Good Clinical Practice) and IRB protocols.

· Maintain participant data such as participant information sheets, consent forms, and data tracking tools.

Required Skills & Qualifications:

• Bachelor’s degree in a health-related field (e.g., Life Sciences, Medicine, Nursing, Public Health, or similar).
• Experience in clinical research or healthcare setting preferred (internships count).
• Knowledge of lab logistics and biospecimen handling.
• Familiarity with CGM devices and mobile health tracking tools is a strong advantage.
• Proficient in using spreadsheets (Excel/Google Sheets), EDC platforms, or research data systems.
• Strong organizational skills and attention to detail.
• Excellent verbal and written communication skills.
• Ability to work independently, manage time efficiently, and multitask across projects.
• Comfortable working with patients remotely and explaining technical processes in simple terms.
• A proactive, empathetic, and collaborative attitude.

Greetings from HCL Technologies!

About the Company

HCL Technologies is a global technology company that helps enterprises reimagine their businesses for the digital age. Our mission is to deliver innovative solutions that drive business transformation and enhance customer experiences.

About the Role

We are looking for talented individuals to join our team and contribute to our mission of delivering exceptional technology solutions.

Responsibilities

• Bachelor’s degree in Life Sciences, Computer Science, or related field.
• 8+ years of experience in clinical data testing and validation.
• Perform UAT for CRF screens, database edit checks, and exceptional reports/listings.
• Test clinical study setup configurations including protocol parameters, visit schedules, and form designs.
• Validate external data acquisition (Lab, ECG, PK/PD) and ensure accurate processing.
• Collaborate with Clinical Data Scientists and Study Data Managers to understand study scope and expectations.
• Strong experience with clinical study setup and CDMS platforms and CTMS
• Review edit check specifications; write and execute UAT scripts.
• Conduct QC on metadata listings and peer review of programming checks.
• Support automation tool validation and standardization of test scripts.
• Ensure consistent use of clinical data standards across programs and repositories.
• Work with Clinical Data Management Systems (e.g., Medidata Rave, Oracle InForm) to validate database builds and data flows.
• Ensure compliance with GxP/GcP and internal SOPs.
• Document and share study-related testing deliverables and lessons learned
• Solid understanding of SDLC, validation methodology, and document management
• .

Pay range and compensation package

The compensation package will be competitive and commensurate with experience.

Equal Opportunity Statement

HCL Technologies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Interested candidates please drop mail to " "

``

Greetings from HCL Technologie!

About the Company

HCL Technologies is a global technology company that helps enterprises reimagine their businesses for the digital age. Our mission is to deliver technology solutions that drive business transformation and create value for our clients.

About the Role

We are looking for a talented individual to join our team and contribute to our mission of delivering innovative technology solutions.

Responsibilities

• Bachelor’s degree in Life Sciences, Computer Science, or related field.
• 6+ years of experience in clinical data testing and validation.
• Perform UAT for CRF screens, database edit checks, and exceptional reports/listings.
• Test clinical study setup configurations including protocol parameters, visit schedules, and form designs.
• Validate external data acquisition (Lab, ECG, PK/PD) and ensure accurate processing.
• Collaborate with Clinical Data Scientists and Study Data Managers to understand study scope and expectations.
• Strong experience with clinical study setup and CDMS platforms and CTMS
• Review edit check specifications; write and execute UAT scripts.
• Conduct QC on metadata listings and peer review of programming checks.
• Support automation tool validation and standardization of test scripts.
• Ensure consistent use of clinical data standards across programs and repositories.
• Work with Clinical Data Management Systems (e.g., Medidata Rave, Oracle InForm) to validate database builds and data flows.
• Ensure compliance with GxP/GcP and internal SOPs.
• Document and share study-related testing deliverables and lessons learned
• Solid understanding of SDLC, validation methodology, and document management

Qualifications

• Bachelor's degree in Computer Science or a related field.
• Relevant certifications are a plus.

Location - PAN INDIA

Pay range and compensation package

The compensation package will be competitive and commensurate with experience.

Equal Opportunity Statement

HCL Technologies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Interested candidate please drop mail to " "

Regards.

Suganya Periyasamy

``