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• 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.

Elevate Your Impact Through Innovation and Learning:

Evalueserve is a global leader in delivering innovative and sustainable solutions to a diverse range of clients, including over 30% of Fortune 500 companies. With presence in more than 45 countries across five continents, we excel in leveraging state-of-the-art technology, artificial intelligence, and unparalleled subject matter expertise to elevate our clients' business impact and strategic decision-making. We have 4,500+ talented professionals operating across 45 countries, including India, China, Chile, Romania, the US, and Canada. Our global network also extends to emerging markets such as Colombia, the Middle East, and the rest of Asia-Pacific. Recognized by Great Place to Work® in India, Chile, Romania, the US, and the UK in 2022, we offer a dynamic, growth-oriented, and open culture that prioritizes flexible work-life balance, diverse and inclusive teams, and equal opportunities for all.

What you will be doing at Evalueserve:

• Pharma Business research and Strategy Consulting support: Define problem statement and initial hypothesis; designing an optimal research approach with a mix of research techniques (e.g., primary/secondary/basic modeling)
• Should be able to structure and present data and results using relevant frameworks
• Ability to arrive at key messages/highlights addressing key objectives as summary of results ready for Executive Leadership consumption
• Presenting results of the research to the client and handling client queries
• Active participation & contribution in team discussions on project specific areas

What we’re Looking for:

• Proven experience in strategy consulting and advisory within the pharmaceutical and biotech sectors, with a strong track record across key project types including opportunity assessment, competitive benchmarking, portfolio optimization, M&A due diligence, go-to-market planning, and go/no-go decision frameworks.
• Deep expertise in primary market research (both qualitative and quantitative), with the ability to apply advanced analytical models and strategic frameworks for data synthesis, trend identification, and triangulation of insights.
• Demonstrated ability to quickly grasp client objectives and deliver high-impact solutions independently or as part of cross-functional teams, ensuring timely and high-quality execution.
• Skilled in developing strategic reports and executive-level presentations, delivering actionable insights and clear recommendations tailored for senior leadership and C-suite stakeholders.
• Strong working knowledge of key pharma and medical data sources, including public databases (e.g., ClinicalTrials.gov, PubMed, FDA, EMA) and commercial platforms (e.g., Citeline, Evaluate Pharma, PharmaTell).
• Analytical and growth-oriented mindset, with a proactive approach to problem-solving and a commitment to delivering value-driven outcomes.
• Excellent written and verbal communication skills, with the ability to convey complex ideas clearly and persuasively.
• Strong interpersonal and collaboration skills, with a focus on active listening, stakeholder engagement, and team synergy.
• Highly organized and time-conscious, with a consistent ability to manage multiple priorities and meet deadlines effectively.
• Proactive contributor to organizational goals, with a keen interest in driving innovation and continuous improvement.
• Proficient in MS Office Suite, particularly PowerPoint and Excel, with strong capabilities in data visualization, report writing, and presentation development
• M.Tech./ M.Pharm/ B.Pharm/ B.Tech (Biotech)/B.E(Biotech)/ MBA
• 6+ years of relevant experience in business research, in Pharmaceutical/ Life Sciences Consulting Organization

Disclaimer: The following job description serves as an informative reference for the tasks you may be required to perform. However, it does not constitute an integral component of your employment agreement and is subject to periodic modifications to align with evolving circumstances.

Please Note: We appreciate the accuracy and authenticity of the information you provide, as it plays a key role in your candidacy. As part of the Background Verification Process, we verify your employment, education, and personal details. Please ensure all information is factual and submitted on time. For any assistance, your TA SPOC is available to support you

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 " "

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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

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