7,013 Cancer Research jobs in India
Clinical Research Scientist
751006 Bhubaneswar, Orissa
₹75000 Annually
WhatJobs
Posted 1 day ago
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Job Description
Our client, a leading name in the pharmaceutical industry, is seeking a highly motivated and accomplished Clinical Research Scientist to join their innovative, fully remote team. This role is critical to the advancement of new therapeutic compounds and requires a candidate with a strong scientific background and experience in clinical trial design and execution. You will be instrumental in overseeing all phases of clinical research, from protocol development to data analysis and reporting, ensuring the highest standards of scientific integrity and regulatory compliance.
Responsibilities:
Responsibilities:
- Design, develop, and implement clinical trial protocols in accordance with regulatory guidelines (e.g., ICH-GCP) and scientific objectives.
- Oversee the conduct of clinical trials, including site selection, initiation, monitoring, and close-out activities.
- Collaborate with cross-functional teams, including medical affairs, regulatory affairs, data management, and biostatistics.
- Analyze and interpret clinical trial data, preparing comprehensive reports for regulatory submissions and scientific publications.
- Ensure compliance with all applicable regulations, ethical standards, and company policies.
- Manage relationships with investigators, clinical research coordinators, and other external stakeholders.
- Contribute to the scientific strategy for drug development programs.
- Prepare and deliver scientific presentations and publications.
- Mentor junior researchers and contribute to a culture of continuous learning and improvement.
- Stay abreast of the latest scientific advancements and therapeutic area developments.
- Ph.D. or M.D. in a life science discipline (e.g., Pharmacology, Biology, Biochemistry, Medicine).
- Minimum of 7 years of experience in clinical research within the pharmaceutical or biotechnology industry.
- Extensive knowledge of clinical trial design, execution, and data analysis.
- Proven experience in protocol development and regulatory submissions.
- Strong understanding of Good Clinical Practice (GCP) and other relevant regulatory requirements.
- Excellent scientific writing and communication skills.
- Demonstrated ability to work effectively in a remote, collaborative environment.
- Strong project management and organizational skills.
- Experience in (Specific therapeutic area, e.g., Oncology, Cardiology) is highly desirable.
- Proficiency in clinical trial management systems and statistical software.
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0
Clinical Research Scientist
160001 Chandigarh, Chandigarh
₹900000 Annually
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Posted 10 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is seeking a talented and dedicated Clinical Research Scientist to join their esteemed research and development team in Chandigarh, Chandigarh, IN . This hybrid role offers the unique opportunity to contribute to cutting-edge drug development while maintaining a flexible work-life balance. You will be responsible for designing, executing, and monitoring clinical trials, ensuring adherence to regulatory standards and company protocols. The ideal candidate will possess a strong scientific background, a meticulous approach to data analysis, and excellent communication skills to collaborate effectively with internal teams and external research sites.
Key responsibilities include:
Key responsibilities include:
- Developing clinical trial protocols and study plans.
- Identifying and selecting suitable clinical investigators and sites.
- Overseeing the conduct of clinical trials, ensuring data integrity and patient safety.
- Monitoring study progress and managing trial budgets.
- Analyzing clinical data and preparing study reports.
- Collaborating with regulatory affairs teams to ensure compliance with local and international regulations (e.g., ICH-GCP).
- Providing scientific expertise and support to project teams.
- Identifying and evaluating new research opportunities and technologies.
- Publishing study findings in peer-reviewed journals and presenting at scientific conferences.
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1
Clinical Research Scientist
530003 Visakhapatnam, Andhra Pradesh
₹750000 Annually
WhatJobs
Posted 18 days ago
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Job Description
Our client is seeking a highly motivated and innovative Clinical Research Scientist to contribute to cutting-edge pharmaceutical research in Visakhapatnam, Andhra Pradesh, IN . This role is crucial for the design, execution, and analysis of clinical trials, aiming to bring life-saving therapies to patients. The successful candidate will work within a multidisciplinary team, collaborating with clinicians, statisticians, and regulatory affairs specialists to ensure the highest standards of scientific rigor and ethical conduct.
Responsibilities:
Responsibilities:
- Contribute to the scientific strategy and protocol development for Phase I-IV clinical trials.
- Oversee the day-to-day scientific conduct of clinical studies, ensuring adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements.
- Collaborate with investigators and site staff to ensure appropriate patient recruitment, data collection, and safety monitoring.
- Analyze and interpret complex clinical data, preparing reports and presentations for internal stakeholders and regulatory submissions.
- Stay current with scientific literature, therapeutic area advancements, and competitive intelligence to identify new research opportunities.
- Prepare scientific publications, abstracts, and presentations for conferences and peer-reviewed journals.
- Provide scientific input for the development of investigational medicinal products (IMPs) and new drug applications (NDAs).
- Manage relationships with external key opinion leaders (KOLs) and academic institutions.
- Ensure the quality and integrity of data generated during clinical trials.
- Participate in regulatory agency interactions and inspections.
- Mentor junior scientists and research associates involved in clinical studies.
- Ph.D. or M.D. in a relevant life science discipline (e.g., Pharmacology, Biology, Medicine).
- Minimum of 3-5 years of experience in clinical research within the pharmaceutical or biotechnology industry.
- Strong understanding of drug development processes, clinical trial design, and regulatory affairs (e.g., FDA, EMA, CDSCO).
- Proven experience in data analysis and interpretation, with proficiency in statistical software or methods.
- Excellent scientific writing and communication skills, demonstrated through publications and presentations.
- Ability to work effectively in a cross-functional team environment.
- Strong project management skills and ability to manage multiple priorities.
- Knowledge of specific therapeutic areas (e.g., oncology, cardiology, neurology) is a plus.
- Experience with electronic data capture (EDC) systems and other clinical trial technologies.
- A proactive and results-oriented approach to scientific challenges.
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2
Clinical Research Scientist
201301 Noida, Uttar Pradesh
₹850000 Annually
WhatJobs
Posted 22 days ago
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Job Description
Our client is looking for a dedicated and experienced Clinical Research Scientist to contribute to groundbreaking pharmaceutical research. This role is based in Noida, Uttar Pradesh, IN , and offers a hybrid work model, blending on-site collaboration with remote flexibility. The successful candidate will play a critical role in designing, implementing, and monitoring clinical trials, ensuring compliance with regulatory guidelines and ethical standards. Key responsibilities include developing study protocols, identifying and recruiting trial sites and investigators, managing study timelines, and analyzing clinical data. You will also be responsible for preparing study reports, regulatory submissions, and ensuring the safety of trial participants. This position requires a deep understanding of pharmaceutical development, clinical trial methodologies, and relevant regulatory frameworks (e.g., ICH-GCP). The ideal candidate will possess excellent scientific acumen, strong project management skills, and the ability to work effectively in a team-oriented environment. A Ph.D. or Master's degree in a relevant scientific discipline (e.g., Pharmacy, Life Sciences, Biotechnology) is preferred. You will collaborate with internal stakeholders, including medical affairs, regulatory affairs, and marketing departments, as well as external partners, such as contract research organizations (CROs) and healthcare professionals. Exceptional communication, presentation, and interpersonal skills are essential for this role. The ability to critically evaluate scientific literature and translate complex findings into actionable insights will be crucial. This is an excellent opportunity to advance your career in the pharmaceutical industry and make a significant impact on patient health.Location: Noida, Uttar Pradesh, IN
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3
Clinical Research Scientist, Oncology
110001 Delhi, Delhi
₹1800000 Annually
WhatJobs
Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a highly skilled and dedicated Clinical Research Scientist to join their cutting-edge oncology research team. This critical position, based in the bustling heart of Delhi, Delhi , will be at the forefront of developing novel cancer therapies. The successful candidate will be responsible for designing, implementing, and managing clinical trial protocols, ensuring adherence to regulatory guidelines and ethical standards. You will play a key role in the entire lifecycle of clinical research, from study design and protocol development to data analysis and reporting. This includes identifying patient populations, developing statistical analysis plans, and interpreting complex clinical data. Collaboration is paramount in this role, as you will work closely with investigators, study coordinators, regulatory affairs, and other internal stakeholders to ensure the successful execution of clinical trials. A deep understanding of oncology, therapeutic areas, and regulatory requirements (e.g., ICH-GCP) is essential. You will contribute to the preparation of regulatory submissions, scientific publications, and presentations at international conferences. The ideal candidate will possess strong analytical, problem-solving, and critical thinking skills, with a meticulous attention to detail. Excellent written and verbal communication skills are crucial for scientific report writing, protocol development, and cross-functional team interactions. We are looking for an individual with a passion for advancing cancer treatment and a commitment to scientific rigor. Experience with early-phase clinical trials and knowledge of statistical software packages are highly advantageous.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Design and develop clinical trial protocols for oncology studies.
- Oversee the execution of clinical trials, ensuring compliance with all regulatory and ethical guidelines.
- Analyze and interpret clinical data, contributing to study reports and publications.
- Collaborate with internal teams and external investigators to manage study conduct.
- Contribute to the preparation of regulatory submission documents.
- Stay abreast of scientific advancements and therapeutic trends in oncology.
- Provide scientific and clinical expertise to cross-functional teams.
- Manage relationships with key opinion leaders and investigators.
Qualifications:
- PhD or MD in a relevant scientific discipline (e.g., Pharmacology, Biology, Medicine).
- Minimum of 7 years of experience in clinical research, with a focus on oncology.
- In-depth knowledge of oncology therapeutic areas and drug development process.
- Strong understanding of ICH-GCP guidelines and regulatory affairs.
- Excellent data analysis, interpretation, and scientific writing skills.
- Proven ability to collaborate effectively in a multidisciplinary team environment.
- Experience with early-phase clinical trials is preferred.
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4
Clinical Research Scientist - Oncology
751001 Bhubaneswar, Orissa
₹70000 Annually
WhatJobs
Posted 4 days ago
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Job Description
Our client, a pioneering pharmaceutical company dedicated to advancing global health, is seeking a highly qualified and driven Clinical Research Scientist to join their oncology division in Bhubaneswar, Odisha, IN . This critical role involves contributing to the design, execution, and analysis of groundbreaking clinical trials aimed at developing novel cancer therapies. The ideal candidate will possess a strong scientific background, extensive experience in clinical research methodology, and a profound understanding of oncology drug development. Responsibilities include protocol development, investigator site selection and management, data interpretation, and regulatory compliance. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and project management, to ensure the successful progression of clinical studies. This position requires a meticulous approach to scientific inquiry, the ability to interpret complex scientific data, and a commitment to ethical research practices. The chosen scientist will play a key role in advancing our client's pipeline of innovative treatments, ultimately impacting patient lives. A strong publication record and experience with IND submissions are highly valued.
Key Responsibilities:
Key Responsibilities:
- Contribute to the design and development of clinical trial protocols for oncology therapeutics.
- Oversee the conduct of clinical trials, ensuring adherence to scientific rigor and regulatory guidelines (e.g., GCP, ICH).
- Identify, evaluate, and select clinical trial sites and investigators.
- Manage relationships with investigators, study coordinators, and key opinion leaders.
- Monitor study progress, analyze emerging data, and identify potential risks or issues.
- Interpret clinical data, contribute to study reports, and present findings at scientific meetings.
- Collaborate with biostatistics and data management teams for data analysis and reporting.
- Ensure compliance with all applicable regulatory requirements and company policies.
- Provide scientific and medical expertise to internal teams and external stakeholders.
- Contribute to the preparation of regulatory submissions (e.g., IND, NDA).
- Ph.D. or M.D. in a relevant life science discipline (e.g., Oncology, Pharmacology, Biology).
- Minimum of 5 years of experience in clinical research, with a specific focus on oncology drug development.
- Proven experience in clinical trial design, execution, and data analysis.
- Strong understanding of cancer biology, therapeutic strategies, and the pharmaceutical drug development process.
- Excellent scientific writing and presentation skills.
- Knowledge of Good Clinical Practice (GCP) and regulatory requirements.
- Ability to work effectively in a collaborative, cross-functional team environment.
- Demonstrated ability to interpret complex scientific data and draw sound conclusions.
- Experience with IND/NDA submissions is a significant advantage.
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5
Clinical Research Scientist - Oncology
110001 Delhi, Delhi
₹1200000 Annually
WhatJobs
Posted 6 days ago
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Job Description
Join a leading pharmaceutical company as a Clinical Research Scientist specializing in Oncology, based in our Delhi, Delhi, IN research facility. This critical role involves the design, execution, and interpretation of clinical trials aimed at developing innovative cancer therapies. You will work closely with cross-functional teams, including medical affairs, regulatory affairs, and data management, to ensure the successful progression of research projects from concept to completion. The ideal candidate will possess a strong scientific background, in-depth knowledge of oncology, and extensive experience in clinical trial management and biostatistics. Responsibilities include developing clinical trial protocols, selecting investigators and sites, monitoring trial progress, analyzing study data, and preparing regulatory submissions. You will also contribute to the scientific strategy for oncology drug development and stay abreast of the latest advancements in the field. A PhD or Master's degree in a relevant life science discipline (e.g., Biology, Pharmacology, Medicine) is required, along with a minimum of 5 years of experience in clinical research, preferably within the pharmaceutical or biotechnology industry. Excellent analytical, written, and verbal communication skills are essential for collaborating with internal teams and external partners, as well as for authoring scientific publications and presentations. This hybrid role offers a blend of in-office laboratory work and strategic planning, with opportunities for remote data analysis and report writing. We are seeking a highly motivated and detail-oriented individual with a passion for advancing cancer treatment. The ability to manage complex projects, interpret complex scientific data, and navigate regulatory landscapes is crucial. If you are a dedicated scientist looking to make a tangible impact on patient lives through groundbreaking research, we invite you to apply.
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6
Clinical Research Scientist - Oncology
411001 Pune, Maharashtra
₹90000 Annually
WhatJobs
Posted 7 days ago
Job Viewed
Job Description
Our client is seeking an experienced Clinical Research Scientist with a specialization in Oncology to join their innovative pharmaceutical team in Pune, Maharashtra, IN . This hybrid role involves a combination of on-site laboratory work and data analysis, with flexibility for remote scientific reporting and literature reviews. You will play a crucial role in designing, executing, and analyzing clinical trials aimed at developing novel cancer therapies. The ideal candidate will have a strong scientific background, a deep understanding of cancer biology, and experience in clinical trial management.
Key Responsibilities:
Key Responsibilities:
- Design and develop clinical trial protocols for oncology therapeutics, ensuring adherence to regulatory guidelines (e.g., ICH-GCP).
- Oversee the execution of clinical trials, including site initiation, monitoring, and data collection.
- Analyze and interpret complex clinical trial data, including efficacy, safety, and pharmacokinetic data.
- Prepare scientific reports, regulatory submissions, and publications summarizing trial results.
- Collaborate with cross-functional teams, including R&D, regulatory affairs, and medical affairs, to advance drug development programs.
- Stay updated on the latest advancements in oncology research, therapeutic targets, and competitive landscape.
- Manage relationships with external investigators, key opinion leaders, and contract research organizations (CROs).
- Contribute to the strategic planning of clinical development programs.
- Ensure compliance with all ethical and regulatory requirements throughout the trial lifecycle.
- Present research findings at scientific conferences and meetings.
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7
Clinical Research Scientist - Oncology
400601 Thane, Maharashtra
₹1300000 Annually
WhatJobs
Posted 8 days ago
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Job Description
Our client is a leading pharmaceutical company seeking a highly motivated and experienced Clinical Research Scientist specializing in Oncology to join their innovative research and development team. This critical role will contribute to the design, execution, and interpretation of clinical trials focused on novel cancer therapies. You will be instrumental in advancing our understanding of oncological diseases and developing life-saving treatments. Responsibilities include developing clinical trial protocols, assessing investigational drug efficacy and safety, and analyzing clinical data to inform strategic decisions. You will collaborate closely with internal teams (e.g., medical affairs, regulatory affairs, statistics) and external partners (e.g., investigators, site staff, CROs) to ensure the successful conduct of trials. A key aspect of this position is staying abreast of the latest scientific advancements, emerging trends, and regulatory requirements in oncology drug development. The ideal candidate will possess a strong scientific background, deep knowledge of cancer biology and clinical trial methodologies, and excellent analytical and communication skills. Experience in data management, statistical analysis, and report writing is essential. This role requires a meticulous approach to research, a commitment to scientific integrity, and the ability to translate complex scientific information into actionable insights. You will contribute to the strategic direction of clinical development programs, ensuring alignment with the company's overall R&D objectives. This is an excellent opportunity for a dedicated scientist to make a significant impact on patient care and the future of cancer treatment within a supportive and collaborative environment.
Responsibilities:
Responsibilities:
- Design, implement, and manage clinical trials in oncology.
- Develop clinical trial protocols and study documents.
- Oversee data collection, analysis, and interpretation for clinical studies.
- Evaluate drug safety and efficacy based on clinical trial results.
- Collaborate with investigators, clinical research associates, and other site personnel.
- Liaise with regulatory authorities and ethics committees.
- Prepare scientific reports, publications, and presentations.
- Stay current with scientific literature and advancements in oncology research.
- Contribute to the strategic planning of clinical development programs.
- Ensure compliance with Good Clinical Practice (GCP) and other regulatory guidelines.
- Ph.D. or M.D. in Life Sciences, Pharmacology, Medicine, or a related field.
- Minimum of 5 years of experience in clinical research, specifically in oncology.
- In-depth knowledge of cancer biology, disease mechanisms, and therapeutic approaches.
- Experience in designing and managing Phase I-IV clinical trials.
- Strong understanding of statistical analysis and data interpretation.
- Proficiency in clinical data management systems and regulatory requirements.
- Excellent written and verbal communication skills.
- Strong analytical and problem-solving abilities.
- Ability to work effectively in a cross-functional team environment.
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8
Clinical Research Scientist, Oncology
600001 Chennai, Tamil Nadu
₹120000 Annually
WhatJobs
Posted 12 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is seeking a talented and motivated Clinical Research Scientist specializing in Oncology to join their dynamic team. This role offers a hybrid work model, allowing for a blend of in-office collaboration and remote flexibility. You will play a crucial role in the design, execution, and analysis of clinical trials for novel cancer therapies, contributing to groundbreaking advancements in patient care. The ideal candidate will possess a strong scientific background, meticulous attention to detail, and a deep understanding of oncology drug development.
Responsibilities:
Responsibilities:
- Contribute to the development and refinement of clinical trial protocols, study plans, and Investigator's Brochures.
- Oversee and manage the conduct of clinical trials, ensuring compliance with GCP, regulatory guidelines, and ethical standards.
- Analyze clinical data, interpret results, and prepare comprehensive study reports.
- Collaborate with cross-functional teams, including medical affairs, regulatory affairs, data management, and clinical operations.
- Liaise with investigators, study coordinators, and clinical research organizations (CROs) to ensure smooth trial execution.
- Review and interpret safety data, identifying potential risks and implementing mitigation strategies.
- Contribute to the preparation of regulatory submissions and scientific publications.
- Stay abreast of the latest scientific literature, clinical trial advancements, and regulatory landscape in oncology.
- Assist in the selection and qualification of clinical trial sites.
- Present study findings at internal meetings and scientific conferences.
- Ph.D. or M.D. in a relevant life science discipline (e.g., Biology, Pharmacology, Medicine).
- Minimum of 3-5 years of experience in clinical research, preferably within the pharmaceutical industry and in oncology.
- Strong understanding of oncology drug development processes and clinical trial methodologies.
- Excellent analytical, problem-solving, and critical thinking skills.
- Proficiency in data analysis and interpretation.
- Strong knowledge of ICH-GCP guidelines and other relevant regulatory requirements.
- Excellent written and verbal communication skills, with the ability to present complex scientific information clearly.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Ability to work effectively in a team environment and manage multiple priorities.
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