1,836 Oncology Research jobs in India
Postdoctoral Fellow - Oncology Research
440001 Nagpur, Maharashtra
₹600000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a renowned research institute, is seeking a dedicated and highly motivated Postdoctoral Fellow to join their cutting-edge Oncology Research division. This position is based in Nagpur, Maharashtra, IN and requires full-time on-site presence to leverage the institute's advanced laboratory facilities and collaborative environment. The successful candidate will contribute to groundbreaking research projects focused on understanding cancer biology, identifying novel therapeutic targets, and developing innovative treatment modalities. This role offers a unique opportunity to work alongside leading oncologists and researchers, publish in high-impact journals, and advance your career in a challenging yet rewarding field.
Responsibilities:
Responsibilities:
- Conduct rigorous scientific research in cancer biology, focusing on molecular mechanisms, signaling pathways, and drug resistance.
- Design, execute, and optimize experimental protocols using advanced techniques in molecular biology, cell biology, and biochemistry.
- Analyze and interpret experimental data, including genomic, proteomic, and phenotypic analyses.
- Troubleshoot experimental challenges and develop innovative solutions.
- Maintain meticulous records of experiments, results, and analyses in electronic lab notebooks.
- Prepare manuscripts for publication in peer-reviewed scientific journals and present research findings at national and international conferences.
- Collaborate with other researchers and clinicians to integrate findings and advance project goals.
- Contribute to grant writing and the development of new research proposals.
- Operate and maintain specialized laboratory equipment.
- Adhere to all laboratory safety protocols and institutional guidelines.
- Ph.D. in Oncology, Molecular Biology, Biochemistry, Pharmacology, or a closely related field.
- Proven experience in cancer research with a strong publication record in reputable journals.
- Hands-on expertise in a range of molecular and cellular biology techniques (e.g., PCR, Western blotting, immunofluorescence, flow cytometry, cell culture, gene editing).
- Proficiency in data analysis software and statistical methods.
- Excellent analytical, critical thinking, and problem-solving skills.
- Strong written and verbal communication skills, with the ability to clearly present complex scientific information.
- Ability to work independently and effectively within a collaborative research team.
- Demonstrated ability to manage research projects and meet deadlines.
- Prior experience with preclinical cancer models (in vivo or in vitro) is advantageous.
This advertiser has chosen not to accept applicants from your region.
0
Senior Clinical Research Scientist - Oncology
682018 Kochi, Kerala
₹1600000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a leading global pharmaceutical company, is actively seeking a highly accomplished Senior Clinical Research Scientist with a specialization in Oncology to join their innovative research division. This is a fully remote position that offers a unique opportunity to contribute to the development of novel cancer therapies. You will be instrumental in designing, executing, and analyzing clinical trials, working closely with a multidisciplinary team of experts to bring life-saving treatments to patients worldwide. Your deep understanding of oncology and clinical development will be key to our client's success.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Lead the design and development of clinical trial protocols for oncology indications, ensuring scientific rigor and alignment with regulatory requirements.
- Provide scientific and medical expertise throughout the clinical trial lifecycle, from protocol concept to final study report.
- Collaborate with investigators, study coordinators, and other clinical personnel to ensure proper trial conduct and data integrity.
- Analyze and interpret complex clinical data, including efficacy and safety endpoints, to inform decision-making.
- Develop scientific publications, abstracts, and presentations based on clinical trial data for peer-reviewed journals and scientific congresses.
- Provide input on the selection of biomarkers and endpoints for clinical studies.
- Stay current with the latest scientific advancements, clinical data, and regulatory guidelines in oncology drug development.
- Contribute to the strategic planning of the oncology pipeline and therapeutic area development.
- Mentor and guide junior scientists and research associates.
Qualifications:
- Ph.D. or M.D. in a relevant life science or medical discipline (e.g., Oncology, Pharmacology, Medicine).
- Minimum of 7 years of progressive experience in clinical research, with a significant focus on oncology clinical trials.
- Extensive knowledge of clinical trial design, execution, and data analysis principles.
- Demonstrated experience in developing clinical protocols and managing the operational aspects of trials.
- Strong understanding of cancer biology, therapeutic mechanisms, and current treatment landscapes.
- Excellent scientific writing and communication skills, with a proven ability to publish research findings.
- Familiarity with regulatory guidelines (e.g., ICH-GCP, FDA, EMA) related to clinical trials.
- Ability to critically evaluate scientific literature and data.
- Proven ability to collaborate effectively in a remote, cross-functional team environment.
This advertiser has chosen not to accept applicants from your region.
1
Senior Clinical Research Scientist - Oncology
201301 Noida, Uttar Pradesh
₹95000 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
Our client, a cutting-edge pharmaceutical company, is seeking a highly motivated and experienced Senior Clinical Research Scientist specializing in Oncology. This is a fully remote position, allowing you to contribute to groundbreaking research from the comfort of your home. You will play a pivotal role in the design, execution, and interpretation of clinical trials for novel oncology therapeutics. Your responsibilities will include developing clinical protocols, overseeing study conduct, analyzing study data, and contributing to regulatory submissions. This role demands a deep understanding of oncology, clinical trial methodologies, and pharmaceutical development. You will collaborate with cross-functional teams, including medical affairs, regulatory affairs, and data management, to ensure the successful progression of clinical programs. The ideal candidate will have a strong scientific background, demonstrated experience in clinical trial management, and a proven track record in oncology research. Excellent written and verbal communication skills are essential for protocol writing, report generation, and stakeholder engagement. We are looking for individuals with a Ph.D. or equivalent in a relevant scientific field. If you are passionate about advancing cancer treatment and thrive in a remote, collaborative environment, this is an exceptional opportunity to make a significant impact on patient lives globally.
This advertiser has chosen not to accept applicants from your region.
2
Clinical Research Associate - Oncology
641001 Coimbatore, Tamil Nadu
₹70000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a leading pharmaceutical company dedicated to advancing cancer therapies, is seeking a highly motivated and experienced Clinical Research Associate (CRA) to join their team in Coimbatore. This on-site position is critical to the successful execution of our clinical trials. As a CRA, you will be responsible for monitoring clinical trial sites to ensure compliance with protocols, regulations, and Good Clinical Practice (GCP) guidelines. Your primary duties will involve site selection, initiation, monitoring, and close-out visits, as well as data verification and query resolution. You will serve as the key liaison between the sponsor and the investigative sites, building strong relationships with investigators and study staff. The ideal candidate will possess a strong understanding of oncology and its related therapeutic areas, coupled with excellent analytical and problem-solving skills. You will be expected to identify and report adverse events and deviations from protocol, ensuring patient safety and data integrity. This role demands meticulous attention to detail, excellent organizational abilities, and the capacity to travel frequently to study sites. If you are passionate about contributing to the development of life-saving drugs and possess the requisite skills and experience, we invite you to apply for this impactful position.
Responsibilities:
Responsibilities:
- Conduct site qualification, initiation, interim monitoring, and close-out visits.
- Verify the accuracy and completeness of clinical trial data by reviewing source documents.
- Ensure compliance with study protocols, Standard Operating Procedures (SOPs), and regulatory requirements (e.g., FDA, ICH-GCP).
- Monitor patient safety and report adverse events and serious adverse events in a timely manner.
- Manage study site activities, including recruitment, screening, and enrollment of participants.
- Provide training and guidance to site staff on study procedures and data collection.
- Resolve data queries and ensure the quality and integrity of the collected data.
- Maintain effective communication with investigators, site staff, and internal project teams.
- Prepare and present monitoring reports and escalate site-specific issues as needed.
- Ensure timely submission of essential documents to regulatory authorities and ethics committees.
- Bachelor's or Master's degree in a life science, nursing, pharmacy, or related field.
- Minimum of 3 years of experience as a Clinical Research Associate, preferably in oncology.
- In-depth knowledge of clinical trial processes, GCP, and regulatory guidelines.
- Experience with oncology clinical trials and understanding of cancer biology.
- Excellent written and verbal communication skills.
- Strong organizational and time management abilities.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to travel frequently to clinical trial sites.
- Critical thinking and problem-solving skills.
This advertiser has chosen not to accept applicants from your region.
3
Clinical Research Associate - Oncology
248001 Dehradun, Uttarakhand
₹800000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is looking for a dedicated and meticulous Clinical Research Associate (CRA) to join their team in Dehradun, Uttarakhand, IN . This role focuses on overseeing clinical trials, ensuring compliance with protocols, and maintaining data integrity for novel oncology treatments. As a CRA, you will be instrumental in the successful execution of clinical studies, from site initiation to study close-out. Your responsibilities will include conducting site visits (monitoring visits) to assess protocol adherence, verifying source data and reports, ensuring patient safety, and managing study documentation. You will serve as the primary liaison between the study sites and the sponsor, providing training and support to site personnel. The ideal candidate will have a Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, or a related field. Significant experience (minimum 3 years) as a CRA or in a clinical research role within the pharmaceutical industry is required, with a strong preference for experience in oncology trials. A thorough understanding of ICH-GCP guidelines, regulatory requirements, and clinical trial processes is essential. Excellent communication, organizational, and interpersonal skills are a must. The ability to travel extensively to clinical sites within the region is required. This is an exciting opportunity to contribute to the development of life-saving cancer therapies and advance your career in clinical research in the picturesque city of Dehradun, Uttarakhand, IN .
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Associate - Oncology
570001 Mysore, Karnataka
₹75000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a progressive pharmaceutical company, is actively recruiting a dedicated Clinical Research Associate (CRA) with a specialization in Oncology to join their clinical operations team. This role, based in Mysuru, Karnataka, IN , offers a hybrid work arrangement, allowing for essential site visits and remote data monitoring. You will play a pivotal role in ensuring the successful execution of oncology clinical trials, adhering to strict regulatory guidelines and ethical standards.
As a Clinical Research Associate, your primary responsibilities will include site selection, initiation, monitoring, and close-out visits for clinical trial sites. You will ensure that clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines. This involves verifying the accuracy and completeness of source data, ensuring proper storage and handling of investigational products, and managing regulatory documentation. You will serve as the primary liaison between the sponsor and the investigative sites, fostering strong working relationships and resolving any issues that may arise during the trial.
The ideal candidate will hold a Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or a related field. A minimum of 3-5 years of experience as a Clinical Research Associate, with specific experience in conducting oncology trials, is required. A comprehensive understanding of GCP, ICH guidelines, FDA regulations, and other relevant regulatory requirements is essential. Strong patient monitoring skills, excellent organizational abilities, meticulous attention to detail, and proficient data management skills are mandatory. Excellent verbal and written communication skills, along with the ability to travel to clinical sites as needed, are crucial for this role. You should possess strong interpersonal skills and the ability to work effectively with diverse teams. This is an exceptional opportunity to contribute to life-saving cancer research and advance your career in clinical development.
As a Clinical Research Associate, your primary responsibilities will include site selection, initiation, monitoring, and close-out visits for clinical trial sites. You will ensure that clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines. This involves verifying the accuracy and completeness of source data, ensuring proper storage and handling of investigational products, and managing regulatory documentation. You will serve as the primary liaison between the sponsor and the investigative sites, fostering strong working relationships and resolving any issues that may arise during the trial.
The ideal candidate will hold a Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or a related field. A minimum of 3-5 years of experience as a Clinical Research Associate, with specific experience in conducting oncology trials, is required. A comprehensive understanding of GCP, ICH guidelines, FDA regulations, and other relevant regulatory requirements is essential. Strong patient monitoring skills, excellent organizational abilities, meticulous attention to detail, and proficient data management skills are mandatory. Excellent verbal and written communication skills, along with the ability to travel to clinical sites as needed, are crucial for this role. You should possess strong interpersonal skills and the ability to work effectively with diverse teams. This is an exceptional opportunity to contribute to life-saving cancer research and advance your career in clinical development.
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Associate, Oncology
700001 Kolkata, West Bengal
₹900000 Annually
WhatJobs
Posted 2 days ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical company, is actively seeking a dedicated and experienced Clinical Research Associate (CRA) to support its groundbreaking oncology clinical trials. This role is based in **Kolkata, West Bengal**, and requires a hands-on approach to study management and oversight. As a CRA, you will play a critical role in ensuring the quality, integrity, and compliance of clinical trial data, adhering strictly to Good Clinical Practice (GCP) guidelines and regulatory requirements. You will be responsible for monitoring investigational sites, verifying patient safety, and ensuring the accurate collection and reporting of trial-related information.
Primary Responsibilities:
Required Qualifications:
Primary Responsibilities:
- Identify, select, and train clinical investigators and site staff.
- Monitor clinical trial sites to ensure adherence to study protocols, GCP, and regulatory guidelines.
- Verify the accuracy, completeness, and integrity of clinical data through source data verification (SDV).
- Ensure patient safety and the ethical conduct of the study at all times.
- Manage study supplies and drug accountability at investigational sites.
- Prepare and present monitoring visit reports.
- Facilitate communication between study sites, the sponsor, and ethics committees.
- Assist in the resolution of site-specific issues and deviations.
- Oversee the informed consent process and ensure its proper documentation.
- Contribute to the development of study-related documents, such as protocols and case report forms (CRFs).
Required Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; advanced degree preferred.
- Minimum of 3 years of experience as a Clinical Research Associate, preferably in oncology trials.
- Thorough understanding of ICH-GCP guidelines and regulatory requirements (e.g., FDA, EMA).
- Demonstrated experience in site monitoring, source data verification, and regulatory compliance.
- Excellent organizational and time management skills.
- Strong written and verbal communication abilities.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to travel to clinical sites as needed.
- Detail-oriented with a high level of accuracy.
- Ability to work independently and as part of a cross-functional team.
This advertiser has chosen not to accept applicants from your region.
Be The First To Know
About the latest Oncology research Jobs in India !
6
Clinical Research Associate - Oncology
110001 Delhi, Delhi
₹65000 month
WhatJobs
Posted 2 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company committed to advancing cancer therapies, is seeking a dedicated and experienced Clinical Research Associate (CRA) to join their clinical operations team in **Delhi, Delhi**. This role is essential for overseeing clinical trials, ensuring adherence to protocols, and maintaining data integrity. The ideal candidate will have a strong background in clinical research, a deep understanding of regulatory requirements, and a passion for contributing to life-saving medical advancements. This position involves significant on-site responsibilities at various study locations.
Responsibilities:
Qualifications:
Responsibilities:
- Monitor clinical trial sites to ensure adherence to study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements.
- Conduct site initiation visits, interim monitoring visits, and close-out visits.
- Verify the accuracy, completeness, and validity of clinical trial data through source document verification.
- Manage investigational product accountability at study sites.
- Train and support study site personnel on protocol requirements and study procedures.
- Build and maintain strong relationships with investigators and site staff.
- Ensure timely reporting of adverse events and protocol deviations.
- Manage site-level regulatory documentation and essential documents.
- Identify site-specific issues and implement corrective and preventive actions (CAPA).
- Contribute to the development of study protocols and clinical trial documents.
Qualifications:
- Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related healthcare field.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
- Thorough understanding of ICH-GCP guidelines and relevant regulatory requirements (e.g., CDSCO in India).
- Experience with oncology clinical trials is highly preferred.
- Proficiency in clinical trial management software (CTMS) and Electronic Data Capture (EDC) systems.
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication skills, with the ability to interact effectively with diverse stakeholders.
- Ability to travel extensively to clinical trial sites.
- Detail-oriented with a commitment to data accuracy and quality.
- Bachelor of Pharmacy or equivalent is a strong advantage.
This advertiser has chosen not to accept applicants from your region.
7
Clinical Research Associate - Oncology
452007 Indore, Madhya Pradesh
₹80000 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
WhatJobs is looking for a dedicated Clinical Research Associate (CRA) with a specialization in Oncology to join our pharmaceutical client's team. This hybrid role is based in Indore, Madhya Pradesh, IN and involves supporting the conduct of clinical trials, ensuring data integrity, patient safety, and adherence to protocols and regulatory guidelines. You will be a key player in bringing life-saving cancer treatments to patients.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Perform site selection, initiation, monitoring, and close-out visits in accordance with Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Ensure that clinical trials are conducted, recorded, and reported in accordance with the protocol, company policies, and applicable regulations.
- Verify the accuracy, completeness, and quality of source data by comparing it with Case Report Forms (CRFs).
- Monitor patient safety and report adverse events and protocol deviations promptly.
- Manage and maintain study documentation, including investigator site files (ISF).
- Train and support study site personnel on protocol requirements and study procedures.
- Act as a liaison between the study site, the sponsor, and the Clinical Research Organization (CRO).
- Ensure all investigational product is handled, stored, and dispensed correctly.
- Prepare monitoring visit reports and follow up on action items with study sites.
- Identify potential risks and issues at study sites and implement corrective and preventive actions.
- Contribute to the development of clinical trial protocols, informed consent forms, and other study documents.
- Participate in investigator meetings and training sessions.
- Maintain communication with the study team regarding site progress and any challenges.
- Uphold the highest ethical standards and ensure patient confidentiality.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field.
- Minimum of 3 years of experience as a Clinical Research Associate, with a significant focus on oncology trials.
- Strong understanding of GCP, ICH guidelines, and other relevant regulatory requirements.
- Proficiency in clinical trial monitoring, data management, and site management.
- Excellent organizational, analytical, and problem-solving skills.
- Strong written and verbal communication skills, with the ability to communicate effectively with site staff and internal teams.
- Proficiency in clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems.
- Ability to travel to study sites as required (approximately 50-70% travel).
- Ability to manage workload effectively and prioritize tasks in a hybrid work environment.
- Familiarity with the Indore clinical research landscape is beneficial.
This advertiser has chosen not to accept applicants from your region.
8
Clinical Research Associate - Oncology
160001 Chandigarh, Chandigarh
₹850000 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical company dedicated to advancing cancer treatments, is seeking a highly motivated Clinical Research Associate (CRA) specializing in Oncology. This remote position allows you to contribute to groundbreaking clinical trials from **Chandigarh, Chandigarh, IN**, and beyond. As a CRA, you will play a vital role in ensuring the quality and integrity of clinical trial data, from site initiation to close-out. You will be responsible for monitoring clinical trial sites, verifying data accuracy, ensuring compliance with protocols and regulations (GCP, ICH), and managing relationships with investigators and site staff. The ideal candidate will possess a strong understanding of clinical trial processes, excellent communication and organizational skills, and a commitment to patient safety. This role demands meticulous attention to detail and the ability to manage multiple studies simultaneously. Key responsibilities include:
Qualifications:
- Monitoring assigned clinical trial sites to ensure compliance with protocols, GCP, and regulatory requirements.
- Verifying the accuracy, completeness, and validity of clinical trial data by reviewing source documents.
- Initiating, monitoring, and closing out clinical investigator sites.
- Identifying and reporting adverse events and protocol deviations.
- Training and supporting site personnel on study-related procedures.
- Maintaining accurate and timely study documentation.
- Building and maintaining strong relationships with investigators and site staff.
- Ensuring efficient trial conduct and timely data collection.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate, with a focus on Oncology trials.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Experience with electronic data capture (EDC) systems.
- Excellent written and verbal communication skills.
- Strong organizational and time management abilities.
- Ability to travel to sites as needed (though the role is primarily remote).
- Proficiency in Microsoft Office Suite.
This advertiser has chosen not to accept applicants from your region.
9