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Bristol-Myers Squibb logo

Clinical Research Physician, Psychiatry

Bristol-Myers Squibb

Clinical Research Physician, Psychiatry

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 28, 2025

Number of Vacancies: 1

Job Description

Provide inputs into clinical plans and protocols with a strong strategic focus based on knowledge of asset/drug, disease area and relevant science in order to meet regulatory and disease strategy targets, in collaboration with China Development Team Provides oversight and medical accountability for a group of studies Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment Support executional delivery of studies (e.g., site activation, enrollment status, as well as adjudication for protocol violations, significant, non-significant deviations etc.) Identifies and builds relationships with principal investigators. Identifies and cultivates thought leaders in order to gain their input on emerging science in drug and biomarker research, disease knowledge, and design of clinical development studies and programs Maintains a strong medical/scientific reputation within the disease area. Has in-depth knowledge of etiology, natural history, diagnosis, and treatment of the disorder. Holds strong expertise in the disease area by attending scientific conferences and ongoing review of literature Keeps abreast of development and regulatory issues related to other competitive or relevant compounds in development and how our portfolio fits into the competitive landscape Provides ongoing medical education to allow for protocol-specific training, supporting the study team, investigators, and others Health Authority Interaction & Publications Contributes to and serves as medical point of expertise in key Health Authority interactions and advisory board meetings as Senior Clinical Trial Physician Authors/drafts clinical content for CSRs, regulatory reports, briefing books and submission documents to support closure, clinical narratives, reporting and filling of the study If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients' lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

About the Role/Company

  • BMS is committed to transforming patients' lives through science
  • BMS promotes a supportive culture that encourages global participation in clinical trials
  • BMS values passion, innovation, urgency, accountability, inclusion, and integrity
  • BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process and ongoing support

Key Responsibilities

  • Provide inputs into clinical plans and protocols with a strategic focus based on knowledge of asset/drug, disease area, and relevant science
  • Lead the analysis of benefit/risk for clinical development protocols in a matrix team environment
  • Support executional delivery of studies including site activation, enrollment status, and adjudication for protocol violations and deviations
  • Identify and build relationships with principal investigators and thought leaders
  • Maintain a strong medical/scientific reputation within the disease area
  • Keep abreast of development and regulatory issues related to competitive or relevant compounds
  • Provide ongoing medical education for protocol-specific training to support the study team, investigators, and others
  • Contribute to and serve as medical point of expertise in key Health Authority interactions and advisory board meetings
  • Author/draft clinical content for CSRs, regulatory reports, briefing books, and submission documents to support study closure, clinical narratives, reporting, and filing

Required Qualifications

  • MD or equivalent medical degree
  • Board certification or eligibility in Psychiatry
  • In-depth knowledge of etiology, natural history, diagnosis, and treatment of psychiatric disorders

Preferred Qualifications

  • Strong expertise in the disease area through attending scientific conferences and ongoing literature review
  • Experience in clinical research and drug development
  • Knowledge of regulatory and development issues related to competitive or relevant compounds

Skills Required

  • Strong strategic focus and ability to meet regulatory and disease strategy targets
  • Ability to lead and provide oversight in a matrix team environment
  • Excellent relationship-building skills with principal investigators and thought leaders
  • Strong communication skills for medical education and Health Authority interactions
  • Proficiency in authoring clinical content for various reports and documents

Benefits & Perks

  • Opportunity to work in a supportive culture that promotes global participation in clinical trials
  • Empowerment to apply individual talents and unique perspectives
  • Shared values of passion, innovation, urgency, accountability, inclusion, and integrity
  • Reasonable workplace accommodations/adjustments for people with disabilities

Additional Requirements

  • Ability to work in a site-by-design role with at least 50% onsite at assigned facility
  • For field-based and remote-by-design roles, ability to physically travel to visit customers, patients, or business partners and attend meetings on behalf of BMS

Locations

  • Beijing, United States

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

250,000 - 350,000 USD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Strong strategic focus and ability to meet regulatory and disease strategy targetsintermediate
  • Ability to lead and provide oversight in a matrix team environmentintermediate
  • Excellent relationship-building skills with principal investigators and thought leadersintermediate
  • Strong communication skills for medical education and Health Authority interactionsintermediate
  • Proficiency in authoring clinical content for various reports and documentsintermediate

Required Qualifications

  • MD or equivalent medical degree (experience)
  • Board certification or eligibility in Psychiatry (experience)
  • In-depth knowledge of etiology, natural history, diagnosis, and treatment of psychiatric disorders (experience)

Preferred Qualifications

  • Strong expertise in the disease area through attending scientific conferences and ongoing literature review (experience)
  • Experience in clinical research and drug development (experience)
  • Knowledge of regulatory and development issues related to competitive or relevant compounds (experience)

Responsibilities

  • Provide inputs into clinical plans and protocols with a strategic focus based on knowledge of asset/drug, disease area, and relevant science
  • Lead the analysis of benefit/risk for clinical development protocols in a matrix team environment
  • Support executional delivery of studies including site activation, enrollment status, and adjudication for protocol violations and deviations
  • Identify and build relationships with principal investigators and thought leaders
  • Maintain a strong medical/scientific reputation within the disease area
  • Keep abreast of development and regulatory issues related to competitive or relevant compounds
  • Provide ongoing medical education for protocol-specific training to support the study team, investigators, and others
  • Contribute to and serve as medical point of expertise in key Health Authority interactions and advisory board meetings
  • Author/draft clinical content for CSRs, regulatory reports, briefing books, and submission documents to support study closure, clinical narratives, reporting, and filing

Benefits

  • general: Opportunity to work in a supportive culture that promotes global participation in clinical trials
  • general: Empowerment to apply individual talents and unique perspectives
  • general: Shared values of passion, innovation, urgency, accountability, inclusion, and integrity
  • general: Reasonable workplace accommodations/adjustments for people with disabilities

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Bristol-Myers Squibb logo

Clinical Research Physician, Psychiatry

Bristol-Myers Squibb

Clinical Research Physician, Psychiatry

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 28, 2025

Number of Vacancies: 1

Job Description

Provide inputs into clinical plans and protocols with a strong strategic focus based on knowledge of asset/drug, disease area and relevant science in order to meet regulatory and disease strategy targets, in collaboration with China Development Team Provides oversight and medical accountability for a group of studies Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment Support executional delivery of studies (e.g., site activation, enrollment status, as well as adjudication for protocol violations, significant, non-significant deviations etc.) Identifies and builds relationships with principal investigators. Identifies and cultivates thought leaders in order to gain their input on emerging science in drug and biomarker research, disease knowledge, and design of clinical development studies and programs Maintains a strong medical/scientific reputation within the disease area. Has in-depth knowledge of etiology, natural history, diagnosis, and treatment of the disorder. Holds strong expertise in the disease area by attending scientific conferences and ongoing review of literature Keeps abreast of development and regulatory issues related to other competitive or relevant compounds in development and how our portfolio fits into the competitive landscape Provides ongoing medical education to allow for protocol-specific training, supporting the study team, investigators, and others Health Authority Interaction & Publications Contributes to and serves as medical point of expertise in key Health Authority interactions and advisory board meetings as Senior Clinical Trial Physician Authors/drafts clinical content for CSRs, regulatory reports, briefing books and submission documents to support closure, clinical narratives, reporting and filling of the study If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients' lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

About the Role/Company

  • BMS is committed to transforming patients' lives through science
  • BMS promotes a supportive culture that encourages global participation in clinical trials
  • BMS values passion, innovation, urgency, accountability, inclusion, and integrity
  • BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process and ongoing support

Key Responsibilities

  • Provide inputs into clinical plans and protocols with a strategic focus based on knowledge of asset/drug, disease area, and relevant science
  • Lead the analysis of benefit/risk for clinical development protocols in a matrix team environment
  • Support executional delivery of studies including site activation, enrollment status, and adjudication for protocol violations and deviations
  • Identify and build relationships with principal investigators and thought leaders
  • Maintain a strong medical/scientific reputation within the disease area
  • Keep abreast of development and regulatory issues related to competitive or relevant compounds
  • Provide ongoing medical education for protocol-specific training to support the study team, investigators, and others
  • Contribute to and serve as medical point of expertise in key Health Authority interactions and advisory board meetings
  • Author/draft clinical content for CSRs, regulatory reports, briefing books, and submission documents to support study closure, clinical narratives, reporting, and filing

Required Qualifications

  • MD or equivalent medical degree
  • Board certification or eligibility in Psychiatry
  • In-depth knowledge of etiology, natural history, diagnosis, and treatment of psychiatric disorders

Preferred Qualifications

  • Strong expertise in the disease area through attending scientific conferences and ongoing literature review
  • Experience in clinical research and drug development
  • Knowledge of regulatory and development issues related to competitive or relevant compounds

Skills Required

  • Strong strategic focus and ability to meet regulatory and disease strategy targets
  • Ability to lead and provide oversight in a matrix team environment
  • Excellent relationship-building skills with principal investigators and thought leaders
  • Strong communication skills for medical education and Health Authority interactions
  • Proficiency in authoring clinical content for various reports and documents

Benefits & Perks

  • Opportunity to work in a supportive culture that promotes global participation in clinical trials
  • Empowerment to apply individual talents and unique perspectives
  • Shared values of passion, innovation, urgency, accountability, inclusion, and integrity
  • Reasonable workplace accommodations/adjustments for people with disabilities

Additional Requirements

  • Ability to work in a site-by-design role with at least 50% onsite at assigned facility
  • For field-based and remote-by-design roles, ability to physically travel to visit customers, patients, or business partners and attend meetings on behalf of BMS

Locations

  • Beijing, United States

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

250,000 - 350,000 USD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Strong strategic focus and ability to meet regulatory and disease strategy targetsintermediate
  • Ability to lead and provide oversight in a matrix team environmentintermediate
  • Excellent relationship-building skills with principal investigators and thought leadersintermediate
  • Strong communication skills for medical education and Health Authority interactionsintermediate
  • Proficiency in authoring clinical content for various reports and documentsintermediate

Required Qualifications

  • MD or equivalent medical degree (experience)
  • Board certification or eligibility in Psychiatry (experience)
  • In-depth knowledge of etiology, natural history, diagnosis, and treatment of psychiatric disorders (experience)

Preferred Qualifications

  • Strong expertise in the disease area through attending scientific conferences and ongoing literature review (experience)
  • Experience in clinical research and drug development (experience)
  • Knowledge of regulatory and development issues related to competitive or relevant compounds (experience)

Responsibilities

  • Provide inputs into clinical plans and protocols with a strategic focus based on knowledge of asset/drug, disease area, and relevant science
  • Lead the analysis of benefit/risk for clinical development protocols in a matrix team environment
  • Support executional delivery of studies including site activation, enrollment status, and adjudication for protocol violations and deviations
  • Identify and build relationships with principal investigators and thought leaders
  • Maintain a strong medical/scientific reputation within the disease area
  • Keep abreast of development and regulatory issues related to competitive or relevant compounds
  • Provide ongoing medical education for protocol-specific training to support the study team, investigators, and others
  • Contribute to and serve as medical point of expertise in key Health Authority interactions and advisory board meetings
  • Author/draft clinical content for CSRs, regulatory reports, briefing books, and submission documents to support study closure, clinical narratives, reporting, and filing

Benefits

  • general: Opportunity to work in a supportive culture that promotes global participation in clinical trials
  • general: Empowerment to apply individual talents and unique perspectives
  • general: Shared values of passion, innovation, urgency, accountability, inclusion, and integrity
  • general: Reasonable workplace accommodations/adjustments for people with disabilities

Target Your Resume for "Clinical Research Physician, Psychiatry" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Clinical Research Physician, Psychiatry. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Clinical Research Physician, Psychiatry" , Bristol-Myers Squibb

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

PharmaceuticalPharmaceuticalHealthcare

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