14 Oncology jobs in Trivandrum
Clinical Research Associate - Oncology
695001 Thiruvananthapuram, Kerala
₹60000 Monthly
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Posted 4 days ago
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Job Description
Our client is actively seeking a dedicated and meticulous Clinical Research Associate (CRA) with expertise in oncology studies to join their growing pharmaceutical research division. This role is crucial in ensuring the successful execution of clinical trials, adhering to strict regulatory guidelines and ethical standards. As a CRA, you will be responsible for monitoring clinical trial sites to ensure data accuracy, patient safety, and protocol compliance. Your duties will include initiating, monitoring, and closing out clinical investigator sites, conducting source data verification, and resolving data discrepancies. You will liaise closely with investigators, study coordinators, and other site staff, providing training on study protocols and regulatory requirements. Travel to clinical trial sites within the designated region, including **Thiruvananthapuram, Kerala, IN**, and potentially other locations, will be a significant part of this role. You will meticulously review trial documentation, including essential documents, investigational product accountability, and regulatory binders, ensuring compliance with Good Clinical Practice (GCP) guidelines and local regulations. A key aspect of the job involves identifying and reporting adverse events and safety concerns in a timely manner. You will also assist in the preparation of study-related documents and contribute to study progress reports. The ideal candidate will possess a strong understanding of oncology drug development, clinical trial processes, and regulatory frameworks (e.g., FDA, ICH-GCP). Excellent organizational, communication, and interpersonal skills are essential for effectively managing multiple sites and building strong relationships with healthcare professionals. A Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field is required, along with prior experience as a CRA or in a clinical research-related role. Experience in oncology is highly preferred. This hybrid role offers a balance between remote work for documentation and reporting, and on-site visits to clinical trial locations.
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Senior Clinical Research Associate - Oncology
695001 Thiruvananthapuram, Kerala
₹70000 Annually
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Posted 1 day ago
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Job Description
Our client, a leading pharmaceutical company, is seeking an experienced Senior Clinical Research Associate (CRA) specializing in Oncology to join their dynamic team in Thiruvananthapuram, Kerala, IN . This hybrid role offers a unique opportunity to contribute to groundbreaking clinical trials that aim to improve patient outcomes in cancer treatment. The Senior CRA will be responsible for overseeing all aspects of clinical trial conduct, ensuring adherence to Good Clinical Practice (GCP) guidelines, protocols, and regulatory requirements. Your duties will include site initiation, monitoring, and close-out visits to ensure data integrity, patient safety, and overall trial compliance. You will serve as the primary liaison between the study sites, the sponsor, and regulatory authorities, fostering strong relationships and effective communication. A significant part of this role involves reviewing and verifying source documents, trial data, and regulatory files, identifying and resolving discrepancies, and ensuring timely reporting of adverse events. The ideal candidate will possess strong organizational skills, meticulous attention to detail, and the ability to manage multiple studies concurrently. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is essential. You will also be involved in training site personnel on trial procedures and ensuring their understanding of protocol requirements. This position demands a proactive approach to problem-solving, identifying potential risks to trial conduct, and implementing mitigation strategies. The ability to travel to study sites as needed (estimated at 50-60%) is a requirement for this hybrid position. We are looking for a dedicated professional who is passionate about advancing cancer research and improving the lives of patients. Your expertise in oncology trials will be invaluable as we strive to bring innovative therapies to market. This role provides a challenging yet rewarding career path within the pharmaceutical industry, offering opportunities for professional growth and development. The successful candidate will be a key player in ensuring the successful execution of critical research.
Responsibilities:
Responsibilities:
- Conduct site initiation, monitoring, and close-out visits in accordance with protocol and GCP.
- Ensure accurate and timely collection and verification of clinical trial data.
- Monitor patient safety and report adverse events according to regulatory guidelines.
- Maintain Trial Master File (TMF) and site essential documents.
- Liaise with investigators, study coordinators, and other site staff.
- Resolve data discrepancies and query issues promptly.
- Train and support site personnel on trial procedures and compliance.
- Contribute to study start-up activities and protocol development.
- Adhere to all company and regulatory policies and procedures.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 5 years of experience as a Clinical Research Associate, with a focus on oncology.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
- Proficiency with EDC and CTMS.
- Excellent communication, interpersonal, and organizational skills.
- Ability to travel up to 60% of the time.
- Strong analytical and problem-solving capabilities.
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1
Senior Clinical Research Associate - Oncology
695001 Thiruvananthapuram, Kerala
₹1200000 Annually
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Posted 18 days ago
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Job Description
Our client, a prominent pharmaceutical company, is seeking a highly skilled Senior Clinical Research Associate (CRA) to join their dedicated clinical operations team. This role operates on a hybrid model, offering flexibility while maintaining essential on-site engagement in Thiruvananthapuram, Kerala, IN . The position focuses on the critical area of oncology research.
As a Senior CRA, you will play a pivotal role in ensuring the successful execution of clinical trials according to Good Clinical Practice (GCP) guidelines and regulatory requirements. Your responsibilities will include site selection, initiation, monitoring, and close-out visits. You will be responsible for verifying data accuracy, ensuring patient safety, and managing site compliance. This involves building strong relationships with investigators and site staff, troubleshooting issues, and ensuring timely data collection and reporting. You will also contribute to the development of study protocols and case report forms, and assist in regulatory submissions.
The ideal candidate will have a strong background in clinical research, with a deep understanding of oncology trials. At least 4-5 years of direct CRA experience is required, demonstrating proficiency in all aspects of clinical trial monitoring. Excellent knowledge of GCP, FDA regulations, and other relevant guidelines is essential. Superior organizational, communication, and interpersonal skills are a must, along with the ability to manage multiple priorities effectively. A Bachelor's degree in a life science, nursing, or a related healthcare field is required; a Master's degree or advanced certification is a plus. This is an excellent opportunity for an experienced CRA to advance their career within a leading pharmaceutical organization, contributing to groundbreaking cancer research in a supportive hybrid work environment.
Key Responsibilities:
As a Senior CRA, you will play a pivotal role in ensuring the successful execution of clinical trials according to Good Clinical Practice (GCP) guidelines and regulatory requirements. Your responsibilities will include site selection, initiation, monitoring, and close-out visits. You will be responsible for verifying data accuracy, ensuring patient safety, and managing site compliance. This involves building strong relationships with investigators and site staff, troubleshooting issues, and ensuring timely data collection and reporting. You will also contribute to the development of study protocols and case report forms, and assist in regulatory submissions.
The ideal candidate will have a strong background in clinical research, with a deep understanding of oncology trials. At least 4-5 years of direct CRA experience is required, demonstrating proficiency in all aspects of clinical trial monitoring. Excellent knowledge of GCP, FDA regulations, and other relevant guidelines is essential. Superior organizational, communication, and interpersonal skills are a must, along with the ability to manage multiple priorities effectively. A Bachelor's degree in a life science, nursing, or a related healthcare field is required; a Master's degree or advanced certification is a plus. This is an excellent opportunity for an experienced CRA to advance their career within a leading pharmaceutical organization, contributing to groundbreaking cancer research in a supportive hybrid work environment.
Key Responsibilities:
- Conduct site selection, initiation, monitoring, and close-out visits for clinical trials.
- Ensure compliance with protocols, GCP, and regulatory requirements.
- Verify the accuracy, completeness, and integrity of clinical trial data.
- Manage and oversee study sites, ensuring efficient trial conduct.
- Build and maintain strong working relationships with investigators, site staff, and study sponsors.
- Identify and resolve site-level issues and deviations.
- Ensure patient safety and protocol adherence at all times.
- Prepare and present monitoring reports to study teams and management.
- Contribute to the development of study documentation and training materials.
- Minimum of 4-5 years of experience as a Clinical Research Associate.
- Proven experience in monitoring oncology clinical trials.
- In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
- Excellent site management and patient safety monitoring skills.
- Strong written and verbal communication skills.
- Ability to manage multiple projects and prioritize effectively.
- Bachelor's degree in life sciences, nursing, or related healthcare field; Master's degree or certification preferred.
- Comfortable working in a hybrid environment with both remote and in-office responsibilities.
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2
Senior Research Scientist - Oncology
695001 Thiruvananthapuram, Kerala
₹120000 Annually
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Posted 10 days ago
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Job Description
Our client is seeking a highly motivated and experienced Senior Research Scientist to join their pioneering oncology drug discovery team. This fully remote role offers an exceptional opportunity to contribute to cutting-edge research from the comfort of your home office. The ideal candidate will possess a deep understanding of molecular biology, cellular assays, and preclinical drug development within the pharmaceutical sector. You will be instrumental in designing, executing, and analyzing complex experiments aimed at identifying and validating novel therapeutic targets.
Responsibilities:
Qualifications:
This role is based in Thiruvananthapuram, Kerala, IN , but operates on a fully remote basis, offering flexibility and work-life balance. Join our dynamic team and make a significant impact on the future of cancer treatment.
Responsibilities:
- Lead the design and execution of in vitro and ex vivo studies to assess the efficacy and mechanism of action of novel drug candidates.
- Develop and optimize cell-based assays for target validation and drug screening.
- Analyze and interpret experimental data, employing advanced statistical methods.
- Collaborate with cross-functional teams, including medicinal chemistry, DMPK, and translational science, to advance projects from discovery through to preclinical development.
- Prepare comprehensive research reports, presentations, and contribute to scientific publications and patent applications.
- Stay abreast of the latest scientific literature and technological advancements in oncology drug discovery.
- Mentor junior scientists and research associates, fostering a collaborative and productive research environment.
- Ensure compliance with all relevant safety regulations and laboratory best practices.
- Maintain detailed and accurate records of all experimental procedures and results.
- Troubleshoot experimental challenges and develop innovative solutions.
Qualifications:
- Ph.D. in Molecular Biology, Cancer Biology, Biochemistry, or a related discipline.
- Minimum of 5 years of postdoctoral or industry research experience in oncology drug discovery.
- Proven track record of successfully leading research projects and contributing to drug candidate progression.
- Extensive experience with mammalian cell culture, aseptic techniques, and various cell-based assay formats (e.g., proliferation, apoptosis, Western blotting, ELISA, flow cytometry).
- Proficiency in data analysis software (e.g., GraphPad Prism, R).
- Excellent written and verbal communication skills, with the ability to present complex scientific information clearly and concisely.
- Demonstrated ability to work independently and collaboratively in a remote setting.
- Strong problem-solving skills and a rigorous scientific approach.
- Experience with in vivo pharmacology studies is a plus.
- Knowledge of bioinformatics tools and techniques is advantageous.
This role is based in Thiruvananthapuram, Kerala, IN , but operates on a fully remote basis, offering flexibility and work-life balance. Join our dynamic team and make a significant impact on the future of cancer treatment.
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Medical Science Liaison (MSL) - Oncology
695001 Thiruvananthapuram, Kerala
₹1100000 Annually
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Posted 10 days ago
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Job Description
Our client, a leading global pharmaceutical company, is seeking a highly qualified and experienced Medical Science Liaison (MSL) to focus on the oncology therapeutic area in the Thiruvananthapuram, Kerala region. This hybrid role involves engaging with key opinion leaders (KOLs) in the medical community, scientific exchange of information, and supporting clinical research initiatives. You will serve as a crucial scientific and clinical resource, building strong relationships with healthcare professionals, researchers, and academic institutions. The ideal candidate will possess a deep understanding of oncology, including disease states, treatment paradigms, and ongoing research, along with excellent communication and presentation skills. Your responsibilities will include presenting complex scientific data, responding to unsolicited medical inquiries, and identifying opportunities for collaborative research. This position requires a proactive approach to staying abreast of the latest scientific advancements and clinical data in oncology. You will be an integral part of the medical affairs team, ensuring that scientific information is accurately and effectively disseminated. We are looking for a highly motivated professional with a strong scientific background and the ability to foster trust and credibility within the medical community. Your contribution will be vital in advancing the understanding and application of our client's innovative oncology treatments.
Key Responsibilities:
Key Responsibilities:
- Engage with Key Opinion Leaders (KOLs) and other healthcare professionals (HCPs) in the oncology field to foster scientific dialogue and exchange of information.
- Present complex scientific data on company products and relevant disease states accurately and compliantly.
- Respond to unsolicited medical and scientific inquiries from KOLs and HCPs.
- Identify and support investigator-initiated research (IIR) opportunities.
- Gather and relay field-based medical insights, competitive intelligence, and emerging scientific trends to internal medical and R&D teams.
- Support the development and execution of regional medical education programs and scientific exchange activities.
- Serve as a scientific resource for internal teams, including marketing, sales, and clinical development.
- Ensure all activities are conducted in compliance with industry regulations, ethical standards, and company policies.
- Identify potential investigators for clinical trials and support clinical trial recruitment efforts.
- Build and maintain strong, credible relationships with key medical stakeholders.
- Contribute to the planning and execution of scientific advisory boards and symposia.
- Prepare and deliver scientific presentations at medical congresses and local meetings.
- Advanced scientific degree (MD, PhD, PharmD, or equivalent) in a relevant life science discipline.
- Minimum of 3-5 years of experience as a Medical Science Liaison (MSL) or in a similar medical affairs role, with a focus on oncology.
- Deep understanding of oncology, including current treatment landscape, clinical trial methodologies, and emerging therapies.
- Exceptional communication, presentation, and interpersonal skills.
- Proven ability to build and maintain strong relationships with key opinion leaders.
- Strong scientific and clinical knowledge base.
- Excellent understanding of regulatory guidelines and ethical conduct in pharmaceutical interactions.
- Ability to travel extensively within the assigned territory and occasionally nationally/internationally.
- Proficiency in MS Office Suite and familiarity with medical affairs databases.
- Strong analytical and problem-solving skills.
- Self-motivated, organized, and able to work independently.
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4
Remote Pharmaceutical Research Scientist - Oncology
695001 Thiruvananthapuram, Kerala
₹90000 Annually
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Posted today
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Job Description
Embark on a groundbreaking career path with our client , a leading innovator in the pharmaceutical sector. We are actively seeking a Remote Pharmaceutical Research Scientist specializing in Oncology to contribute to our cutting-edge drug discovery and development programs. In this fully remote position, you will leverage your scientific expertise to design, conduct, and analyze experiments aimed at identifying novel therapeutic targets and developing innovative cancer treatments. Your responsibilities will encompass a broad range of activities, including in-vitro and in-vivo study design, data interpretation, literature reviews, and contributing to scientific publications and patent applications. You will collaborate closely with a multidisciplinary team of scientists, clinicians, and project managers, utilizing advanced research methodologies and technologies. The ideal candidate possesses a strong foundation in cancer biology, molecular pharmacology, and medicinal chemistry, with a demonstrated ability to generate high-quality research data. This role requires a highly analytical and results-oriented individual who can work independently, manage multiple projects simultaneously, and thrive in a virtual research environment. You will play a pivotal role in advancing our oncology pipeline, from early-stage research through preclinical development. Your insights and contributions will be instrumental in shaping the future of cancer therapy. We are looking for a scientist who is passionate about making a tangible impact on patient lives through scientific excellence and a commitment to innovation. The ability to critically evaluate scientific literature, design robust experimental protocols, and effectively communicate complex scientific findings both orally and in writing is paramount. This is a unique opportunity to drive significant progress in oncology research from the convenience of your home office.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Design and execute in-vitro and in-vivo experiments to investigate novel oncology targets.
- Analyze experimental data, interpret results, and draw scientific conclusions.
- Conduct comprehensive literature reviews to identify research opportunities and stay abreast of industry trends.
- Contribute to the preparation of research reports, scientific publications, and patent applications.
- Collaborate with cross-functional teams, including biologists, chemists, and clinicians.
- Utilize advanced techniques in molecular biology, cell biology, and pharmacology.
- Manage multiple research projects and prioritize tasks effectively.
- Communicate research findings and progress to internal stakeholders and external collaborators.
- Ensure compliance with all relevant ethical and regulatory guidelines.
- Contribute to the development of preclinical drug candidates.
- Stay current with the latest advancements in oncology research and drug development.
Qualifications:
- Ph.D. in Cancer Biology, Molecular Pharmacology, Biochemistry, or a related field.
- Minimum of 3-5 years of postdoctoral or industry research experience in oncology.
- Proven track record of successful research, evidenced by publications in reputable journals.
- Extensive knowledge of cancer biology, signaling pathways, and therapeutic modalities.
- Hands-on experience with relevant in-vitro and in-vivo models.
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication skills.
- Ability to work independently and as part of a remote, collaborative team.
- Proficiency in data analysis software and bioinformatics tools.
- Experience with drug discovery and development processes is a plus.
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5
Senior Pharmaceutical Research Scientist - Oncology
695001 Thiruvananthapuram, Kerala
₹1200000 Annually
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Posted 1 day ago
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Job Description
Our client is seeking a highly motivated and experienced Senior Pharmaceutical Research Scientist specializing in Oncology to join their cutting-edge, fully remote research team. This pivotal role will contribute to the discovery and development of novel therapeutics targeting various cancer types. You will be instrumental in designing and executing complex experimental protocols, analyzing vast datasets, and collaborating with cross-functional teams to advance drug candidates through the pipeline. The ideal candidate will possess a deep understanding of cancer biology, molecular pathways, and drug discovery principles. Responsibilities include:
Qualifications:
- Designing and conducting in vitro and in vivo experiments to assess drug efficacy and mechanisms of action.
- Developing and validating assays for target identification and validation.
- Interpreting experimental results, troubleshooting technical challenges, and proposing innovative solutions.
- Collaborating with medicinal chemists, pharmacologists, and toxicologists to guide lead optimization.
- Preparing comprehensive reports, scientific publications, and presentations for internal and external stakeholders.
- Mentoring junior scientists and contributing to a collaborative research environment.
- Staying abreast of the latest scientific literature and emerging trends in oncology drug discovery.
- Ensuring all research activities comply with regulatory guidelines and company policies.
- Maintaining accurate and detailed laboratory records.
- Participating in strategic planning for research projects and portfolio development.
Qualifications:
- Ph.D. in Pharmacology, Molecular Biology, Biochemistry, or a related life science discipline.
- Minimum of 5-7 years of post-doctoral research experience in the pharmaceutical industry or a related field, with a strong focus on oncology.
- Proven track record of successfully contributing to drug discovery programs.
- Expertise in cancer cell culture, molecular biology techniques (e.g., PCR, Western blotting, ELISA), and flow cytometry.
- Experience with various cancer models (e.g., xenografts, PDX models) is highly desirable.
- Excellent analytical and problem-solving skills.
- Strong written and verbal communication skills, with the ability to present complex scientific data clearly.
- Demonstrated ability to work independently and collaboratively in a remote setting.
- Proficiency in data analysis software (e.g., GraphPad Prism, R).
- Familiarity with bioinformatics tools and genomic/proteomic data analysis is a plus.
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6
Senior Pharmaceutical Research Scientist - Oncology
695001 Thiruvananthapuram, Kerala
₹150000 Annually
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Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical company at the forefront of medical innovation, is seeking a highly skilled and dedicated Senior Pharmaceutical Research Scientist to join their cutting-edge research and development team. This exciting opportunity is based in Thiruvananthapuram, Kerala . You will be instrumental in designing and executing complex research projects focused on discovering and developing novel oncology therapeutics. Your responsibilities will include leading in-vitro and in-vivo studies, analyzing experimental data, interpreting results, and contributing to the development of preclinical and clinical drug candidates. The ideal candidate will possess a Ph.D. in Pharmacology, Molecular Biology, Biochemistry, or a related life science discipline, with a minimum of 5-7 years of post-doctoral research experience in oncology drug discovery. Proven expertise in cancer biology, target validation, and assay development is essential. You must demonstrate a strong understanding of drug development processes, regulatory requirements, and scientific literature. Excellent laboratory skills, including experience with relevant instrumentation and techniques, are required. The ability to critically evaluate scientific data, present findings clearly and concisely, and publish research in high-impact journals is expected. This role requires strong leadership qualities, the ability to mentor junior scientists, and collaborate effectively with cross-functional teams. We are looking for a highly motivated and innovative scientist with a passion for advancing cancer treatment and a commitment to scientific excellence. This position offers a challenging and rewarding environment to contribute to life-saving therapies.
Location: Thiruvananthapuram, Kerala, IN
Location: Thiruvananthapuram, Kerala, IN
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7
Principal Pharmaceutical Research Scientist - Oncology
695001 Thiruvananthapuram, Kerala
₹1800000 Annually
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Posted 3 days ago
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Job Description
Our client, a leading global pharmaceutical innovator, is seeking a highly accomplished Principal Pharmaceutical Research Scientist specializing in Oncology to join their esteemed research division. This role is fully remote, allowing you to contribute your expertise from anywhere within India, collaborating with world-class scientists. You will be at the forefront of discovering and developing novel therapeutics for cancer, leading critical research projects from discovery through early-stage development. Your responsibilities will encompass designing and executing innovative in vitro and in vivo studies, identifying novel drug targets, validating therapeutic approaches, and contributing to the strategic direction of the oncology pipeline. As a Principal Scientist, you will leverage your deep understanding of cancer biology, drug discovery principles, and pharmaceutical development processes. This role demands a strong scientific track record, demonstrated ability to lead complex research programs, and expertise in preclinical oncology models. You will mentor junior scientists, collaborate effectively across interdisciplinary teams (including chemistry, pharmacology, and translational medicine), and contribute significantly to scientific publications and patent applications. The ability to interpret complex data, make critical decisions, and drive projects forward with minimal supervision is essential. Responsibilities will include:
- Leading and executing research projects focused on novel oncology drug discovery.
- Designing and performing complex in vitro and in vivo experiments using state-of-the-art technologies.
- Identifying and validating novel oncology targets and therapeutic strategies.
- Interpreting experimental data, drawing robust conclusions, and presenting findings to internal stakeholders.
- Developing and optimizing preclinical models for efficacy and safety assessment.
- Collaborating closely with medicinal chemists, pharmacologists, and translational scientists.
- Contributing to the preparation of regulatory submissions and scientific publications.
- Mentoring and guiding junior research staff.
- Staying current with the latest advancements in oncology and drug discovery.
- Ph.D. in Oncology, Molecular Biology, Pharmacology, or a related life sciences discipline.
- Minimum of 8 years of post-doctoral or industry experience in pharmaceutical R&D, with a strong focus on oncology drug discovery.
- Proven track record of leading successful research projects and delivering key milestones.
- Extensive experience with various oncology models (cell lines, xenografts, syngeneics, etc.).
- Deep understanding of cancer biology, tumor immunology, and molecular targeted therapies.
- Proficiency in relevant molecular and cellular biology techniques.
- Excellent data analysis, interpretation, and problem-solving skills.
- Strong publication record in high-impact peer-reviewed journals.
- Exceptional written and verbal communication skills, with the ability to present complex scientific information effectively.
- Demonstrated ability to work independently and collaboratively in a remote research environment.
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8
Principal Pharmaceutical Research Scientist - Oncology
695001 Thiruvananthapuram, Kerala
₹120000 Annually
WhatJobs
Posted 5 days ago
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Job Description
Our client, a leading innovator in the pharmaceutical industry, is seeking a highly accomplished Principal Pharmaceutical Research Scientist specializing in Oncology to join their esteemed research team in Thiruvananthapuram, Kerala . This senior-level position is critical for driving forward groundbreaking research and development of novel cancer therapies. The ideal candidate will possess a deep understanding of oncology, a passion for scientific discovery, and a proven ability to lead complex research projects from conception to potential clinical application.
Responsibilities:
Responsibilities:
- Lead and execute cutting-edge research projects focused on identifying and validating new therapeutic targets in oncology.
- Design and conduct in vitro and in vivo studies to evaluate the efficacy and safety of novel drug candidates.
- Develop and optimize biochemical and cellular assays for high-throughput screening and lead compound characterization.
- Analyze complex experimental data, interpret results, and generate comprehensive reports and presentations.
- Collaborate effectively with cross-functional teams, including medicinal chemistry, pharmacology, toxicology, and clinical development.
- Stay abreast of the latest scientific literature and industry trends in oncology and drug discovery.
- Mentor and guide junior scientists, fostering a collaborative and innovative research environment.
- Contribute to the intellectual property strategy by identifying patentable inventions and preparing invention disclosures.
- Present research findings at scientific conferences and contribute to peer-reviewed publications.
- Ensure compliance with all relevant regulatory guidelines and ethical standards in research.
- Ph.D. in Molecular Biology, Cancer Biology, Pharmacology, Biochemistry, or a related field.
- A minimum of 8-10 years of post-doctoral research experience in the pharmaceutical industry or academia, with a strong focus on oncology.
- Demonstrated expertise in cancer biology, drug discovery, and translational research.
- Proven experience in designing and managing complex research projects, with a track record of successful outcomes.
- Extensive experience with various biological assays, cell culture techniques, and animal models relevant to oncology.
- Excellent understanding of drug development processes and regulatory requirements.
- Exceptional data analysis, critical thinking, and problem-solving skills.
- Strong publication record and experience presenting at international conferences.
- Excellent written and verbal communication skills, with the ability to communicate complex scientific information clearly.
- Demonstrated leadership potential and experience in mentoring junior researchers.
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