MD Job at Bristol Myers Squibb | Apply Now
MD job opportunities in clinical research and drug development are rapidly growing as pharmaceutical companies expand their global trials. One such exciting opportunity is now open at Bristol Myers Squibb, where professionals with medical expertise can contribute to life-changing innovations. The company is currently hiring an Associate Director, Senior Clinical Scientist in Hyderabad, offering experienced physicians the chance to work in advanced clinical research programs in oncology and other therapeutic areas.
Job Details:
- Job Position: Associate Director, Senior Clinical Scientist
- Company: Bristol Myers Squibb
- Location: Hyderabad, Telangana, India
- Job ID: R1598023
About the Company:
Bristol Myers Squibb is a globally recognized biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines for patients with serious diseases. With a strong focus on scientific research and patient care, the company works across multiple therapeutic areas including oncology, immunology, cardiovascular diseases, and hematology. The organization is widely known for transforming scientific discoveries into life-changing treatments. The company also promotes work-life balance and provides competitive benefits, career growth opportunities, and a collaborative workplace culture.
Job Description:
The Senior Clinical Scientist works within the Clinical Science function and provides scientific expertise required to design and deliver clinical studies and programs. In this MD job, the candidate will be responsible for implementing, planning, and executing assigned clinical trial activities while serving as a Clinical Trial Lead for one or more studies. The role involves coordinating with cross-functional teams, guiding clinical scientists, and ensuring successful clinical trial operations.
This oncology job offers an opportunity to participate in clinical development strategies and contribute to innovative drug development programs.
Qualifications and Experience:
- Medical qualification (MD) in Pharmacology, Oncology, or Hematology preferred
- Minimum 10+ years of experience in clinical science, clinical research, or related areas
- Proven experience leading scientific interactions with regulatory bodies such as DCGI
- Experience in oncology and hematology therapeutic areas preferred
- Strong understanding of GCP/ICH guidelines, drug development processes, and clinical study design
- Expertise in clinical data review, trend analysis, and interpretation
- Knowledge of data monitoring committees and independent response adjudication committees
- Familiarity with tools such as Microsoft Word, Excel, PowerPoint, Electronic Data Capture systems (e.g., RAVE), and J-Review
- Ability to travel domestically and internationally if required
Key Responsibilities:
- Maintain a thorough understanding of assigned clinical trial protocols and requirements.
- Educate and guide supporting team members regarding protocol execution.
- Plan and lead interactions with local health authorities and Subject Expert Committees.
- Lead study start-up, conduct, and close-out activities for assigned trials.
- Collaborate with Medical Monitors and Clinical Development Leads to evaluate innovative trial designs.
- Write, review, and resolve cross-functional comments on clinical protocols.
- Conduct site-facing activities such as investigator training and responding to clinical queries.
- Participate in case report form (CRF) design and clinical data review.
- Identify clinical data trends and escalate questions to the Medical Monitor.
- Develop clinical narrative plans and review clinical narratives.
- Provide information required for trial budgets and CRO scope of work.
- Draft and review Clinical Study Reports (CSRs) and regulatory documents such as Investigator Brochures (IB) and DSURs.
- Collaborate with external partners and serve as the scientific liaison.
