11 Oncology jobs in Kanpur

• Conduct pre-study, initiation, interim monitoring, and close-out visits at clinical trial sites to assess trial conduct and compliance.
• Verify the accuracy and completeness of clinical data by reviewing source documents and electronic data capture (EDC) systems.
• Ensure adherence to protocol requirements, Good Clinical Practice (GCP), ICH guidelines, and all applicable regulatory requirements.
• Build and maintain strong relationships with investigators and site staff, providing guidance and support.
• Train site personnel on study procedures, regulatory requirements, and data collection processes.
• Identify, document, and track deviations and adverse events, ensuring timely reporting.
• Prepare monitoring reports and communicate findings and action plans to study teams and management.
• Manage site supplies and essential regulatory documents.
• Contribute to the development of clinical study protocols and Case Report Forms (CRFs).
• Participate in remote team meetings and contribute to study strategy discussions.
• Perform remote data review and analysis as part of the hybrid work model.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. Advanced degree is a plus.
• Minimum of 3-5 years of experience as a Clinical Research Associate (CRA), with a strong focus on Oncology trials.
• In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
• Proven experience in conducting site monitoring visits and managing clinical trial data.
• Excellent understanding of clinical trial processes from initiation to close-out.
• Strong analytical and problem-solving skills, with meticulous attention to detail.
• Exceptional written and verbal communication skills, including report writing.
• Proficiency in using clinical trial management software (CTMS) and Electronic Data Capture (EDC) systems.
• Ability to travel to investigational sites as required (estimated 50-60% travel).
• Effective organizational and time management skills, with the ability to manage multiple priorities.
• This role is based in Kanpur, Uttar Pradesh, IN , with a hybrid work arrangement.

• Conduct site selection, initiation, interim monitoring, and close-out visits in accordance with protocol and GCP requirements.
• Verify the accuracy, completeness, and validity of clinical data by reviewing source documents and case report forms (CRFs).
• Ensure adherence to protocol, investigational plan, and applicable regulations.
• Train and mentor site staff on study procedures, data collection, and regulatory compliance.
• Identify, track, and resolve site-level issues and discrepancies in a timely manner.
• Manage communication between the sponsor and investigational sites, serving as the primary point of contact.
• Oversee the safety reporting process at investigational sites, ensuring timely reporting of adverse events.
• Prepare monitoring visit reports and follow up on action items.
• Ensure timely drug/investigational product accountability at the sites.
• Contribute to the development and review of study-related documents, including protocols, CRFs, and informed consent forms.
• Maintain effective working relationships with investigators, site staff, and internal project teams.
• Stay updated on oncology research advancements and regulatory requirements.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific discipline.
• Minimum of 5 years of experience as a Clinical Research Associate, with a significant focus on oncology trials.
• In-depth knowledge of ICH-GCP guidelines and other relevant regulatory requirements (e.g., FDA, EMA, CDSCO).
• Proven experience in conducting site monitoring visits and managing multiple clinical sites.
• Excellent understanding of clinical trial processes and documentation.
• Strong medical terminology knowledge, particularly in oncology.
• Exceptional organizational, communication, and interpersonal skills.
• Proficiency in clinical data management systems and electronic data capture (EDC) tools.
• Ability to work independently, manage time effectively, and travel occasionally as needed (post-pandemic).
• Demonstrated problem-solving skills and attention to detail.
• Adaptability and willingness to work in a remote-first environment.

• Lead and conduct advanced research projects focused on novel oncology targets and drug candidates.
• Design, optimize, and execute in vitro and in vivo assays to evaluate drug efficacy and safety.
• Analyze and interpret complex biological data, employing statistical methods and bioinformatics tools.
• Prepare detailed research reports, scientific publications, and regulatory submission documents.
• Collaborate effectively with internal teams and external partners to drive research objectives.
• Stay abreast of the latest scientific literature and technological advancements in oncology research.
• Mentor and guide junior research staff, fostering a culture of scientific excellence.
• Ensure compliance with all laboratory safety regulations and ethical guidelines.

• Ph.D. in Pharmacology, Molecular Biology, Cancer Biology, or a related life science discipline.
• Minimum of 5-7 years of post-doctoral or industry research experience in oncology drug discovery.
• Proven track record of success in publishing research findings in reputable peer-reviewed journals.
• Extensive experience with various cellular and molecular biology techniques.
• Familiarity with preclinical models of cancer and PK/PD studies.
• Excellent written and verbal communication skills.
• Ability to think critically and solve complex scientific problems.

• Lead and execute research projects focused on identifying and validating novel oncology drug targets.
• Design, optimize, and perform complex biochemical and cellular assays to assess compound efficacy and mechanism of action.
• Develop and implement in vivo models for preclinical testing of therapeutic agents.
• Analyze and interpret experimental data, present findings at team meetings, and contribute to scientific publications and patent applications.
• Collaborate with cross-functional teams, including medicinal chemistry, pharmacology, and clinical development, to advance drug candidates.
• Stay abreast of the latest scientific literature and technological advancements in oncology research and drug discovery.
• Mentor junior scientists and provide technical guidance.
• Ensure compliance with all relevant regulatory guidelines and company policies.

• Ph.D. in Pharmacology, Molecular Biology, Biochemistry, or a related field.
• Minimum of 5-7 years of post-doctoral or industry experience in pharmaceutical research, with a strong focus on oncology.
• Proven track record in drug discovery and development, with hands-on experience in relevant assay development and validation.
• Expertise in cancer biology, signal transduction pathways, and immunology.
• Proficiency in bioinformatic tools and statistical analysis.
• Excellent communication, presentation, and interpersonal skills.
• Ability to work independently and collaboratively in a remote setting.
• Strong problem-solving skills and a results-oriented approach.
• Experience with AAV, CRISPR, or other gene editing technologies is a plus.

• Developing and validating novel assays for target identification and validation.
• Conducting in vitro studies using cancer cell lines to assess compound efficacy and mechanism of action.
• Designing and performing in vivo efficacy studies in relevant animal models of cancer.
• Analyzing and interpreting complex experimental data using statistical and bioinformatics tools.
• Collaborating with cross-functional teams to progress drug candidates towards clinical development.
• Preparing manuscripts for publication in peer-reviewed journals and presenting findings at scientific conferences.
• Maintaining detailed and accurate laboratory notebooks and research records.
• Ensuring compliance with all ethical and regulatory guidelines for preclinical research.

• Design, execute, and interpret complex experiments to identify and validate novel oncology targets and pathways.
• Develop and implement robust in vitro and in vivo models for evaluating the efficacy and mechanism of action of potential drug candidates.
• Lead cross-functional research teams comprising biologists, chemists, pharmacologists, and toxicologists.
• Manage external research collaborations with academic institutions and contract research organizations (CROs).
• Contribute to the preparation of regulatory documents, patent applications, and scientific publications.
• Evaluate and integrate new technologies and methodologies to enhance drug discovery efforts.
• Critically assess data, identify project risks, and propose innovative solutions to overcome scientific challenges.
• Mentor junior scientists and foster a collaborative and intellectually stimulating research environment.
• Stay abreast of the latest advancements in oncology research, targeted therapies, and drug discovery technologies.
• Effectively present research findings and strategic recommendations to senior management and scientific advisory boards.

• Ph.D. in Oncology, Molecular Biology, Biochemistry, Pharmacology, or a related life science discipline.
• Minimum of 5 years of post-doctoral or industry experience in oncology drug discovery.
• Demonstrated success in leading drug discovery projects and advancing candidates into preclinical development.
• Expertise in one or more areas of oncology research such as tumor immunology, signaling pathways, or drug resistance mechanisms.
• Proficiency in cell-based assays, in vivo pharmacology models, and other relevant drug discovery techniques.
• Strong understanding of medicinal chemistry principles and drug development processes.
• Excellent analytical, critical thinking, and problem-solving skills.
• Exceptional written and verbal communication skills, with a proven ability to publish and present scientific findings.
• Experience managing CROs and external collaborations.
• Ability to thrive in a fast-paced, innovative, and remote work environment.

Need Urgent requirement Consultant Medical Oncology For Hospital Moradabad UP AND Rohtak Haryana, Kanpur.

Experience : years

Education :- DM/DNB

Salary : LPM (Negotiable)

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Location: Remote (India)

Work Hours: U.S. business hours (evening/night shifts in India)

DAVA Oncology , a rapidly growing oncology-focused consulting firm headquartered in Dallas, Texas , is seeking motivated and detail-oriented Scientific Program Associates to join our Oncology Meeting Innovations (OMI) team.

This role involves supporting the development, coordination, and execution of virtual oncology programs and regional colloquia that bring together leading oncologists and researchers from across the world. Candidates will contribute to research, content development, and program support activities that drive meaningful collaboration in the oncology community.

• Conduct scientific and clinical research across oncology therapeutic areas using peer-reviewed literature, trial registries, and conference proceedings.
• Synthesize complex oncology data into concise and relevant insights for program discussions, reports, and speaker materials.
• Support the planning and execution of OMI’s virtual and regional programs — preparing agendas, discussion guides, and event summaries.
• Collaborate with cross-functional teams to ensure scientific accuracy , consistency, and timely delivery of program materials.
• Track and summarize key developments in oncology research, emerging therapies, and conference outcomes.
  

• Master’s degree in Life Sciences, Biotechnology, Molecular Biology, Pharmacology, Biochemistry, or a related field.
• 1+ year of experience or internship in research analysis, scientific communication, clinical research, or oncology-related work preferred.
• Strong ability to interpret clinical trial data and scientific literature.
• Familiarity with medical conferences, academic publications, or scientific event coordination is advantageous.

• Excellent written and verbal communication in English.
• Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint).
• Strong analytical, organizational, and multitasking abilities.
• Capacity to work independently and manage tight deadlines.
• Must be available to work during U.S. time zones (evening/night shifts in India).