61 Oncology jobs in Mumbai

Description

Lead India R&D Strategy and Execution

Work closely with OTAU GPTs a and Global R&D functions to optimize integrated India development strategy for pipeline assets

Monitor overall country performance and support country focused oncology activities e.g. feasibility and site selections to deliver country operational milestones

Serve as the internal expert on India’s clinical development to inform global development strategy. Collaborate closely with India LOC to execute One Oncology strategy in India including tapping into local expertise and community networks

Collaborate and work closely with Oncology GPTs, the Global R&D team and regional teams, as appropriate, for each asset or indications under the remit

Engage study investigators to maintain strong interest and focus on Takeda’s oncology clinical trials

Proactively build and maintain strong investigator networks in India to support current and future trials across Takeda’s oncology portfolio in both solid tumors and hematologic malignancies and proactively share with the OTAU and Global teams

Build and scale global clinical trial capabilities in India as a key market in collaboration with LOC, Region and Global teams to accelerate Takeda innovation and boost efficiency

Clinical Development team participation and leadership

Leads the Development Team in India for assigned compounds. In some cases may lead clinical directors or clinical scientist(s) responsible for leading this team with an emphasis on proactively identifying contingencies, risks, and mitigation strategies.

Directs Development Team strategy and deliverables overseeing the Development Strategy, Clinical Development Plan and Clinical Protocols in India. Recommends scope, complexity and size, which influence the budget of all aspects of a program. Provides continual critical and constructive evaluation of the development strategy to maintain a state-of-the-art development plan that is competitive and consistent with the latest regulatory requirements, proactive identification of challenges, and development of contingency plans to meet them.

Responsible for high impact India specific decisions: monitoring and interpreting data from ongoing internal and external studies, assessing the medical and scientific implications and making recommendations that impact regional and global development such as “go/no go” decisions or modification of development plans or study designs that may have a significant impact on timelines or product labeling. Plans clinical development strategies in context of medical/clinical significance considering how a given product will fit in with current treatments, standard of care, and unmet medical need.

C. Synopsis / Protocol Development, Study Execution, & Study Interpretation

Trial Medical Monitoring

External Interactions

Due Diligence, Business Development and Alliance Projects

Leadership, Task Force Participation, Upper Management Accountability

Lead India Oncology Clinical Science team

Serving as Country Matter Expert

Lead and develop oncology clinical strategies for India according to business needs as assigned

Education, Experience, Knowledge and Skills:

Skills

Knowledge

TRAVEL REQUIREMENTS:

Locations

Mumbai, India

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

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**Job Description**
Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Senior Medical Director, Clinical Science - Oncology in our Mumbai office.
At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver **_Better Health and a Brighter Future_** to people around the world.
Here, you will be a vital contributor to our inspiring, bold mission.
**Objective / Purpose:** .
+ **Lead and strengthen OTAU R&D capabilities in India** to maximize the value for accelerating global innovation and efficiency, in alignment with global OTAU R&D goals.
+ **Ensure effective oncology operations in India** by leveraging local opportunities and overseeing all OTAU Clinical Science activities in India. Be accountable for speed and quality in collaboration with the global OTAU team and, as appropriate, OTAU-China, OTAU-Japan and other global R&D functions.
+ **Partner with ISEA and India LOC leaders** to enhance enterprise-level efforts for accelerating global clinical trials.
**Accountabilities:**
**Lead India OTAU R&D Strategy and Execution**
+ Work closely with OTAU GPTs and Global R&D functions to optimize integrated India development strategy for pipeline assets.
+ Monitor overall country performance and support country-focused oncology activities e.g. feasibility and site selections to deliver country operational milestones.
+ Serve as the internal expert on India's oncology clinical development environment to inform global development strategy. Collaborate closely with India LOC to execute Enterprise Engagement model in India including tapping into local expertise and community networks.
+ Collaborate and work closely with Oncology GPTs, the Global R&D team and regional teams, as appropriate, for each asset or indications under the remit.
+ Engage study investigators to maintain strong interest and focus on Takeda's oncology clinical trials.
+ Proactively build and maintain strong investigator networks in India to support current and future trials across Takeda's oncology portfolio in both solid tumors and hematologic malignancies and proactively share with the OTAU and Global teams.
+ Build and scale global clinical trial capabilities in India as a key market in collaboration with LOC, Region and Global teams to accelerate Takeda innovation and boost efficiency.
**Clinical Development team participation and leadership**
+ Leads the Development Team in India (US, EU, Japan) for assigned compounds. In some cases may lead clinical directors or clinical scientist(s) responsible for leading this team with an emphasis on proactively identifying contingencies, risks, and mitigation strategies.
+ Directs Development Team strategy and deliverables overseeing the Development Strategy, Clinical Development Plan and Clinical Protocols. Recommends scope, complexity and size, which influence the budget of all aspects of a program. Provides continual critical and constructive evaluation of the development strategy to maintain a state-of-the-art development plan that is competitive and consistent with the latest regulatory requirements, proactive identification of challenges, and development of contingency plans to meet them.
+ Responsible for high impact India specific decisions: monitoring and interpreting data from ongoing internal and external studies, assessing the medical and scientific implications and making recommendations that impact regional and global development such as "go/no go" decisions or modification of development plans or study designs that may have a significant impact on timelines or product labeling. Plans clinical development strategies in context of medical/clinical significance considering how a given product will fit in with current treatments, standard of care, and unmet medical need.
**Synopsis / Protocol Development, Study Execution, & Study Interpretation**
+ Leads Oncology Clinical Science activities in India, including protocol development, study execution, and data interpretation.
+ Serves as an advisor to the clinical scientists involved in these activities, and be accountable to senior company management for the successful completion of underlying objectives. For the assigned compounds, accountable for the successful completion of projects undertaken - and for pro-active contingency planning / interventions necessary to ensure achievement of related goals.
+ Interprets data from an overall scientific standpoint as well as within the context of the medical significance to individual patients.
**Trial Medical Monitoring**
+ Oversees medical monitoring activities, assessing issues related to protocol conduct and/or individual subject safety. Assesses overall safety information for studies and compounds in conjunction with Pharmacovigilance.
**External Interactions**
+ Leads KOL and investigator engagement strategies to support development of assigned compounds, and contributes to regulatory strategy in India.
+ Provides leadership and serves as an advisor to the other clinical physicians and scientists engaged in these activities and, in the context of these responsibilities, will be accountable to senior leadership for the successful completion of related objectives in India.
**Due Diligence, Business Development and Alliance Projects**
+ Responsible for identification and evaluation of potential business development opportunities, conducts due diligence evaluations, and development and negotiation of clinical development plans for potential alliances and or in-licensing opportunities, as assigned. As part of a global due diligence team, assesses scientific, medical, and development feasibility, evaluating strategic fit with overall portfolio, evaluating complete or ongoing clinical trials, assessing regulatory interactions and future development plans, interacting with upper management of potential partner/acquisition companies during DD visits and alliance negotiations, and representing clinical science on internal assessment teams in conjunction with BD teams
+ As assigned, serves as clinical point of contact for ongoing alliance projects and interfaces with partner to achieve Takeda's strategic goals while striving to maintain good working relationship between Takeda and partner. Provides guidance to clinical scientists who are involved in some of these activities.
**Leadership, Task Force Participation, Upper Management Accountability**
+ Interacts directly with research division based on pertinent clinical and development expertise and with NPP to provide knowledge/understanding of India market environment. Represents clinical science on high impact/priority task forces across the organization or external to the company.
+ Hires, manages, mentors, motivates, empowers, develops and retains staff to support assigned activities. Drives performance management, career development, and team engagement.
**Lead India Oncology Clinical Science team**
+ Build, manage/oversee and engage the India R&D members.
+ Foster a high-performing team culture with a focus on development, well-being, and alignment with OTAU's mission.
**Serving as Country Matter Expert**
+ Be a strong advocate for the Takeda ONE Oncology and R&D organizations in India in collaboration with India LOC; serve as local bridge for any future opportunities in engaging India innovation ecosystem.
+ Point for escalation for resolution of complex country related issues & risk and serve as a site escalation point for oncology investigator concerns.
+ Lead and develop oncology clinical strategies for India according to business needs as assigne **d**
**Education & Competencies :**
**Education, Experience, Knowledge and Skills:**
+ MD, combined MD/PhD or internationally recognized equivalent.
+ Clinical Training in Malignant Hematology and/or Medical Oncology preferred.
+ Minimum 5 to 7 years of clinical research experience in the pharmaceutical industry, CRO health-related consulting company, or biomedical/clinical experience within academia (or a combination of aforementioned).
+ Minimum of 4 to 5 years of people management experience in a healthcare or life sciences setting.
+ Proven success in leading global or regional clinical development teams, including responsibility for multi-regional studies. Experience beyond US/EU is a plus.
+ Experience with NDA/MAA Submission preferred.
+ Demonstrated ability to lead and manage cross-functional medical, scientific and technical teams.
+ Superior communication, strategic, interpersonal and negotiating skills
+ Ability to anticipate challenges and drive proactive problem-solving
+ Ability to drive decision-making within matrixed multi-regional teams
+ Diplomacy and positive influencing abilities across diverse cultures
+ Solid teamwork, organizational, interpersonal, and problem-solving skills; exercises good judgment with respect to Takeda confidential information and strategies
+ Fluent business English (oral and written) and strong medical writing capabilities
+ Deep understanding of oncology therapeutic areas, including mechanisms of action relevant to assigned compounds.
+ Strong knowledge of global regulatory and compliance requirements, including but not limited to ICH GCP; awareness of local country requirements is essential.
+ Familiarity with emerging research trends in designated therapeutic area
**TRAVEL REQUIREMENTS:**
+ Ability to drive to or fly to various meetings or client sites, including overnight trips. Some international travel may be required.
+ Requires approximately 15 - 25% travel.
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law
This position is currently classified as "hybrid" in accordance with Takeda's Hybrid and Remote Work policy.
#LI-JT1
**Locations**
Mumbai, India
**Worker Type**
Employee
**Worker Sub-Type**
Regular
**Time Type**
Full time

Description

Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Senior Medical Director, Clinical Science - Oncology in our Mumbai office.

At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver to people around the world.

Here, you will be a vital contributor to our inspiring, bold mission.

Objective / Purpose: .

Lead and strengthen OTAU R&D capabilities in India to maximize the value for accelerating global innovation and efficiency, in alignment with global OTAU R&D goals.

Ensure effective oncology operations in India by leveraging local opportunities and overseeing all OTAU Clinical Science activities in India. Be accountable for speed and quality in collaboration with the global OTAU team and, as appropriate, OTAU-China, OTAU-Japan and other global R&D functions.

Partner with ISEA and India LOC leaders to enhance enterprise-level efforts for accelerating global clinical trials.

Accountabilities:
 

Lead India OTAU R&D Strategy and Execution

Work closely with OTAU GPTs and Global R&D functions to optimize integrated India development strategy for pipeline assets.

Monitor overall country performance and support country-focused oncology activities e.g. feasibility and site selections to deliver country operational milestones.

Serve as the internal expert on India’s oncology clinical development environment to inform global development strategy. Collaborate closely with India LOC to execute Enterprise Engagement model in India including tapping into local expertise and community networks.

Collaborate and work closely with Oncology GPTs, the Global R&D team and regional teams, as appropriate, for each asset or indications under the remit.

Engage study investigators to maintain strong interest and focus on Takeda’s oncology clinical trials.

Proactively build and maintain strong investigator networks in India to support current and future trials across Takeda’s oncology portfolio in both solid tumors and hematologic malignancies and proactively share with the OTAU and Global teams.

Build and scale global clinical trial capabilities in India as a key market in collaboration with LOC, Region and Global teams to accelerate Takeda innovation and boost efficiency.

Clinical Development team participation and leadership

Leads the Development Team in India (US, EU, Japan) for assigned compounds. In some cases may lead clinical directors or clinical scientist(s) responsible for leading this team with an emphasis on proactively identifying contingencies, risks, and mitigation strategies.

Directs Development Team strategy and deliverables overseeing the Development Strategy, Clinical Development Plan and Clinical Protocols. Recommends scope, complexity and size, which influence the budget of all aspects of a program. Provides continual critical and constructive evaluation of the development strategy to maintain a state-of-the-art development plan that is competitive and consistent with the latest regulatory requirements, proactive identification of challenges, and development of contingency plans to meet them.

Responsible for high impact India specific decisions: monitoring and interpreting data from ongoing internal and external studies, assessing the medical and scientific implications and making recommendations that impact regional and global development such as “go/no go” decisions or modification of development plans or study designs that may have a significant impact on timelines or product labeling. Plans clinical development strategies in context of medical/clinical significance considering how a given product will fit in with current treatments, standard of care, and unmet medical need.

Synopsis / Protocol Development, Study Execution, & Study Interpretation

Leads Oncology Clinical Science activities in India, including protocol development, study execution, and data interpretation.

Serves as an advisor to the clinical scientists involved in these activities, and be accountable to senior company management for the successful completion of underlying objectives. For the assigned compounds, accountable for the successful completion of projects undertaken - and for pro-active contingency planning / interventions necessary to ensure achievement of related goals.

Interprets data from an overall scientific standpoint as well as within the context of the medical significance to individual patients.

Trial Medical Monitoring

Oversees medical monitoring activities, assessing issues related to protocol conduct and/or individual subject safety. Assesses overall safety information for studies and compounds in conjunction with Pharmacovigilance.

External Interactions

Leads KOL and investigator engagement strategies to support development of assigned compounds, and contributes to regulatory strategy in India.

Provides leadership and serves as an advisor to the other clinical physicians and scientists engaged in these activities and, in the context of these responsibilities, will be accountable to senior leadership for the successful completion of related objectives in India.

Due Diligence, Business Development and Alliance Projects

Responsible for identification and evaluation of potential business development opportunities, conducts due diligence evaluations, and development and negotiation of clinical development plans for potential alliances and or in-licensing opportunities, as assigned. As part of a global due diligence team, assesses scientific, medical, and development feasibility, evaluating strategic fit with overall portfolio, evaluating complete or ongoing clinical trials, assessing regulatory interactions and future development plans, interacting with upper management of potential partner/acquisition companies during DD visits and alliance negotiations, and representing clinical science on internal assessment teams in conjunction with BD teams

As assigned, serves as clinical point of contact for ongoing alliance projects and interfaces with partner to achieve Takeda’s strategic goals while striving to maintain good working relationship between Takeda and partner. Provides guidance to clinical scientists who are involved in some of these activities.

Leadership, Task Force Participation, Upper Management Accountability

Interacts directly with research division based on pertinent clinical and development expertise and with NPP to provide knowledge/understanding of India market environment. Represents clinical science on high impact/priority task forces across the organization or external to the company.

Hires, manages, mentors, motivates, empowers, develops and retains staff to support assigned activities. Drives performance management, career development, and team engagement.

Lead India Oncology Clinical Science team

Build, manage/oversee and engage the India R&D members.

Foster a high-performing team culture with a focus on development, well-being, and alignment with OTAU’s mission.

Serving as Country Matter Expert

Be a strong advocate for the Takeda ONE Oncology and R&D organizations in India in collaboration with India LOC; serve as local bridge for any future opportunities in engaging India innovation ecosystem.

Point for escalation for resolution of complex country related issues & risk and serve as a site escalation point for oncology investigator concerns.

Lead and develop oncology clinical strategies for India according to business needs as assigned

Education & Competencies :
 

Education, Experience, Knowledge and Skills:

MD, combined MD/PhD or internationally recognized equivalent.

Clinical Training in Malignant Hematology and/or Medical Oncology preferred.

Minimum 5 to 7 years of clinical research experience in the pharmaceutical industry, CRO health-related consulting company, or biomedical/clinical experience within academia (or a combination of aforementioned).

Minimum of 4 to 5 years of people management experience in a healthcare or life sciences setting.

Proven success in leading global or regional clinical development teams, including responsibility for multi-regional studies. Experience beyond US/EU is a plus.

Experience with NDA/MAA Submission preferred.

Demonstrated ability to lead and manage cross-functional medical, scientific and technical teams.

Superior communication, strategic, interpersonal and negotiating skills

Ability to anticipate challenges and drive proactive problem-solving

Ability to drive decision-making within matrixed multi-regional teams

Diplomacy and positive influencing abilities across diverse cultures

Solid teamwork, organizational, interpersonal, and problem-solving skills; exercises good judgment with respect to Takeda confidential information and strategies

Fluent business English (oral and written) and strong medical writing capabilities

Deep understanding of oncology therapeutic areas, including mechanisms of action relevant to assigned compounds.

Strong knowledge of global regulatory and compliance requirements, including but not limited to ICH GCP; awareness of local country requirements is essential.

Familiarity with emerging research trends in designated therapeutic area

TRAVEL REQUIREMENTS:

Ability to drive to or fly to various meetings or client sites, including overnight trips. Some international travel may be required.

Requires approximately 15 - 25% travel.

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law

This position is currently classified as “hybrid” in accordance with Takeda’s Hybrid and Remote Work policy. 

#LI-JT1

Locations

Mumbai, India

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Our client, a leading pharmaceutical company, is seeking a highly experienced Senior Clinical Research Associate (CRA) to contribute to groundbreaking oncology trials. This role involves overseeing and managing clinical research studies, ensuring compliance with protocols, regulatory requirements, and ethical standards. The Senior CRA will be responsible for site selection, initiation, monitoring, and close-out activities, ensuring the quality, integrity, and accuracy of the data collected. You will serve as the primary point of contact between the study sites and the sponsor, building strong relationships with investigators and site staff. Key responsibilities include conducting on-site and remote monitoring visits, verifying source documents against case report forms (CRFs), and ensuring adherence to Good Clinical Practice (GCP) guidelines. The Senior CRA will also be involved in training site personnel, addressing protocol deviations, and resolving study-related issues promptly. A critical part of this role is to ensure timely recruitment of patients and to manage the overall progress of the study at assigned sites. We are looking for a detail-oriented, organized, and proactive individual with a strong understanding of clinical trial processes, particularly within the oncology therapeutic area. Excellent communication, negotiation, and problem-solving skills are essential for success in this demanding but rewarding position. This is an excellent opportunity for a seasoned CRA to advance their career in a dynamic and innovative pharmaceutical environment. The position is fully remote, allowing you to manage your responsibilities from anywhere, with occasional travel to sites as needed. This flexibility empowers you to focus on delivering high-quality clinical trial oversight.

Key Responsibilities:

• Plan, execute, and manage clinical trial monitoring activities.
• Conduct on-site and remote monitoring visits to ensure protocol compliance.
• Verify source data and case report forms (CRFs) for accuracy and completeness.
• Ensure adherence to Good Clinical Practice (GCP) and regulatory requirements.
• Manage relationships with investigators, site staff, and study sponsors.
• Facilitate site selection, initiation, and close-out procedures.
• Oversee patient recruitment and study progress at assigned sites.
• Address protocol deviations and resolve study-related issues.
• Train site personnel on study protocols and procedures.
• Prepare monitoring reports and communicate findings to relevant parties.

Qualifications:

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
• Minimum of 5 years of experience as a Clinical Research Associate.
• Extensive experience in oncology clinical trials is mandatory.
• Thorough understanding of GCP, ICH guidelines, and regulatory requirements.
• Proven ability to conduct site monitoring and data verification.
• Excellent communication, interpersonal, and organizational skills.
• Ability to work independently and manage time effectively in a remote setting.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Willingness to travel occasionally to clinical sites.

Our client, a leading pharmaceutical company dedicated to advancing healthcare through groundbreaking research, is seeking an experienced Senior Clinical Research Scientist specializing in Oncology. This hybrid role, based in Mumbai, Maharashtra, IN , requires a deep understanding of clinical trial design, execution, and data analysis within the oncology therapeutic area. You will play a pivotal role in the development of novel cancer therapies, contributing to critical decision-making processes from early-stage research through to regulatory submission.

Your responsibilities will include designing and overseeing clinical trial protocols, developing statistical analysis plans, and interpreting complex clinical data to assess drug efficacy and safety. You will collaborate closely with cross-functional teams, including biostatisticians, medical monitors, regulatory affairs, and project management, to ensure the successful execution of trials. The ideal candidate will possess a strong scientific background, a comprehensive understanding of oncology, and expertise in Good Clinical Practice (GCP) guidelines. You will contribute to the preparation of regulatory documents, scientific publications, and presentations for internal and external stakeholders.

The successful candidate will hold a Ph.D. or a Master's degree in a relevant life science discipline (e.g., Pharmacology, Biomedical Sciences, Medicine), with a minimum of 6 years of experience in clinical research within the pharmaceutical industry, with a specific focus on oncology drug development. Proven experience in designing and managing Phase I, II, or III clinical trials is essential. You should possess exceptional analytical, critical thinking, and problem-solving skills, with a meticulous approach to data interpretation and scientific rigor. Strong written and verbal communication skills are necessary for effective collaboration and dissemination of scientific findings. This role requires a proactive, self-motivated individual who can thrive in a dynamic, collaborative research environment.

Responsibilities:

• Design and develop clinical trial protocols for oncology studies.
• Develop statistical analysis plans and interpret clinical trial data.
• Oversee the execution of clinical trials, ensuring adherence to protocols and GCP.
• Collaborate with biostatisticians, medical monitors, and other study team members.
• Assess drug safety and efficacy based on clinical data.
• Contribute to the preparation of regulatory submission documents.
• Author scientific publications and present research findings.
• Stay updated on the latest advancements in oncology research and clinical development.
• Provide scientific and technical guidance to clinical research teams.
• Contribute to the strategic direction of oncology drug development programs.

Qualifications:

• Ph.D. or Master's degree in Life Sciences, Pharmacology, Medicine, or a related field.
• Minimum of 6 years of experience in clinical research within the pharmaceutical industry, with a focus on oncology.
• Proven experience in designing and managing clinical trials (Phase I-III).
• Strong understanding of oncology, clinical pharmacology, and drug development processes.
• Knowledge of Good Clinical Practice (GCP) guidelines.
• Excellent analytical, critical thinking, and problem-solving skills.
• Strong scientific writing and presentation abilities.
• Effective communication and interpersonal skills.
• Ability to work effectively in a hybrid research environment.

Our client, a leading pharmaceutical innovator, is seeking a highly experienced Senior Clinical Research Scientist specializing in Oncology to join their dynamic team in Mumbai, Maharashtra, IN . This is an exciting opportunity to contribute to cutting-edge drug development and make a significant impact on patient lives. The successful candidate will play a pivotal role in the design, execution, and interpretation of clinical trials for novel cancer therapies. Responsibilities include developing clinical trial protocols, overseeing study conduct, analyzing and interpreting complex data sets, and preparing scientific reports and regulatory submissions. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, data management, and biostatistics, to ensure the successful progression of clinical development programs. The ideal candidate will possess a strong understanding of oncology drug development, regulatory guidelines (e.g., ICH-GCP), and statistical principles. A Ph.D. or Master's degree in a life science discipline, combined with a minimum of 5-7 years of relevant experience in clinical research within the pharmaceutical industry, is essential. Excellent communication, problem-solving, and leadership skills are also required. This role offers a competitive salary, comprehensive benefits, and opportunities for professional growth within a globally recognized organization. If you are passionate about advancing cancer treatment and possess the requisite expertise, we encourage you to apply. Your expertise will be crucial in driving our oncology pipeline forward and delivering life-changing medicines to patients in need.

Key Responsibilities:

• Design and develop clinical trial protocols and study documents for oncology indications.
• Provide scientific and strategic input into all phases of clinical development.
• Oversee the execution of clinical trials, ensuring adherence to protocols and regulatory requirements.
• Analyze and interpret clinical trial data, preparing comprehensive reports and publications.
• Collaborate with internal and external stakeholders to ensure efficient trial management.
• Stay abreast of scientific advancements and regulatory changes in oncology.
• Contribute to regulatory submissions and interact with health authorities.
• Mentor junior scientific staff and contribute to team development.

Qualifications:

• Ph.D. or Master's degree in a relevant life science field.
• Minimum of 5-7 years of progressive experience in clinical research, with a focus on oncology.
• In-depth knowledge of oncology drug development, clinical trial design, and statistical analysis.
• Familiarity with global regulatory requirements and ICH-GCP guidelines.
• Proven ability to manage complex projects and lead cross-functional teams.
• Exceptional analytical, written, and verbal communication skills.
• Demonstrated ability to work independently and collaboratively in a fast-paced environment.

Our client, a leading pharmaceutical innovator, is seeking a highly skilled Senior Clinical Research Scientist specializing in Oncology to join their dedicated research and development team. This hybrid role will involve designing, implementing, and overseeing clinical trial protocols for novel cancer therapies. You will play a critical role in analyzing trial data, interpreting results, and preparing comprehensive scientific reports and publications. Responsibilities include collaborating with cross-functional teams, including medical affairs, regulatory affairs, and drug development, to ensure the successful progression of research programs. You will contribute to the strategic planning of clinical development, identify potential risks and challenges, and propose innovative solutions.

The ideal candidate will possess a strong scientific background, with a Ph.D. or equivalent in a relevant life science discipline, and extensive experience in oncology clinical research. Proven expertise in protocol development, study design, statistical analysis interpretation, and regulatory submission requirements is essential. Excellent written and verbal communication skills are required to effectively present complex scientific information to diverse audiences, including regulatory agencies and scientific peers. You will be expected to stay abreast of the latest advancements in oncology research and clinical practice. This role requires a meticulous approach to data integrity and a commitment to ethical research conduct. While the role offers a hybrid work model, providing flexibility and collaboration opportunities, you will be expected to attend critical meetings and site visits as needed in **Thane, Maharashtra, IN**. This is an exciting opportunity to make a significant impact on patient lives through groundbreaking pharmaceutical research.