Resume and JobRESUME AND JOB
Bristol-Myers Squibb logo

Sr Manager, Line Manager, CDM

Bristol-Myers Squibb

Sr Manager, Line Manager, CDM

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 24, 2025

Number of Vacancies: 1

Job Description

Manager, Line Manager-Clinical Data Management is a leadership role providing program leadership and potential line management responsibility considered essential to the sustainability and success of the BMS R&D pipeline. Responsibilities will include, but are not limited to: Line Management Line management responsibility of Data Management Data Review staff based on business requirements Manages the resource assignments ensuring appropriate support is in place to provide data quality oversight for clinical trials Forecast's future resource needs based on the book of work and initiatives; proposing solutions to meet potential resource constraints Assigns resources to initiatives in line with their development plans and providing appropriate guidance to staff to influence results and drive to completion Works proactively with staff to understand individual strengths, opportunities, and career goals; supporting development of plans that capitalize on strengths and address opportunities; providing regular feedback to promote development. Effectively coaches and mentors' staff, seeking out training opportunities where needed, to develop the next generation leaders. Develops and promotes a workplace culture that values diversity of thought, promotes integrity, creates accountability, supports effective decision making, and provides opportunities to grow. Using clear communications and collaborative strategies to drive to resolution Authors procedural documents (SOPs, work instructions, job aids) and coordinating reviews/approvals. Ensuring procedural documents are reflective of industry standards and regulatory requirements, include optimal processes and are regularly maintained. Bachelor's Degree required with an advanced degree preferred. Minimal 6 years of relevant industry experience with strong line management experience. Communicate effectively with senior management and crossfunctional teams. Solid knowledge of submission requirements, [e.g. New Drug Application (NDA)/Biologics License Application (BLA)/Market Authorization Application (MAA)] Solution oriented mindset and ability to drive change. Proven time management skills and ability to be flexible to meet job demands, manage multiple priorities, and take on new initiatives and improvement efforts. Demonstrates a high level of adaptability in dealing with ambiguous and complex work environment and balances multiple demands on role in a responsive and professional manner. Ability to sustain high levels of performance in a constantly changing environment. Travel required , 5-10% Industry Conferences, Investigator Meetings, Regulatory Inspections (as needed) 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. Strong experience in program governance in all phases of clinical trials for Clinical Data Management delivery. Strong experience in managing Clinical Data Review teams across therapeutic areas. Able to work collaboratively on multi-disciplinary project teams and develop productive relationships with external vendors. Sound knowledge of Clinical Drug Development Process, regulatory and ICH guidelines (e.g. EMEA, FDA) and industry standard practices regarding data management. Strong knowledge and experience of EDC systems (Medidata RAVE preferred); demonstrated knowledge of Microsoft Office skills and well versed in industry trends and emerging technologies supporting data collection. Strong project management; Exhibits expertise in metrics analysis and reporting methodologies.

About the Role/Company

  • BMS is dedicated to transforming patients' lives through science
  • Every BMS employee plays an integral role in work that goes far beyond ordinary
  • BMS empowers individual talents and unique perspectives in a supportive culture
  • BMS promotes global participation in clinical trials
  • BMS values passion, innovation, urgency, accountability, inclusion, and integrity
  • BMS is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments, and ongoing support in their roles
  • BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws
  • BMS will never request payments, financial information, or social security numbers during the application or recruitment process
  • Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations

Key Responsibilities

  • Line management responsibility of Data Management Data Review staff
  • Manage resource assignments to ensure appropriate support for data quality oversight in clinical trials
  • Forecast future resource needs based on the book of work and initiatives
  • Propose solutions to meet potential resource constraints
  • Assign resources to initiatives in line with their development plans
  • Provide appropriate guidance to staff to influence results and drive to completion
  • Work proactively with staff to understand individual strengths, opportunities, and career goals
  • Support development of plans that capitalize on strengths and address opportunities
  • Provide regular feedback to promote development
  • Effectively coach and mentor staff, seeking out training opportunities where needed
  • Develop and promote a workplace culture that values diversity of thought, promotes integrity, creates accountability, supports effective decision making, and provides opportunities to grow
  • Use clear communications and collaborative strategies to drive to resolution
  • Author procedural documents (SOPs, work instructions, job aids) and coordinate reviews/approvals
  • Ensure procedural documents are reflective of industry standards and regulatory requirements, include optimal processes, and are regularly maintained
  • Work collaboratively on multi-disciplinary project teams and develop productive relationships with external vendors

Required Qualifications

  • Bachelor's Degree required
  • Minimum 6 years of relevant industry experience
  • Strong line management experience

Preferred Qualifications

  • Advanced degree preferred
  • Strong experience in program governance in all phases of clinical trials for Clinical Data Management delivery
  • Strong experience in managing Clinical Data Review teams across therapeutic areas
  • Strong knowledge and experience of EDC systems (Medidata RAVE preferred)

Skills Required

  • Communicate effectively with senior management and cross-functional teams
  • Solid knowledge of submission requirements (e.g., New Drug Application (NDA)/Biologics License Application (BLA)/Market Authorization Application (MAA))
  • Solution-oriented mindset and ability to drive change
  • Proven time management skills
  • Ability to be flexible to meet job demands, manage multiple priorities, and take on new initiatives and improvement efforts
  • High level of adaptability in dealing with ambiguous and complex work environment
  • Ability to balance multiple demands on role in a responsive and professional manner
  • Ability to sustain high levels of performance in a constantly changing environment
  • Sound knowledge of Clinical Drug Development Process, regulatory and ICH guidelines (e.g., EMEA, FDA), and industry standard practices regarding data management
  • Demonstrated knowledge of Microsoft Office skills
  • Well versed in industry trends and emerging technologies supporting data collection
  • Strong project management
  • Exhibits expertise in metrics analysis and reporting methodologies

Benefits & Perks

  • Uniquely interesting work, life-changing careers
  • Supportive culture promoting global participation in clinical trials
  • Shared values of passion, innovation, urgency, accountability, inclusion, and integrity
  • Opportunity to transform your life and career
  • Reasonable workplace accommodations/adjustments for people with disabilities
  • Transparent recruitment process
  • Ongoing support in roles for people with disabilities

Additional Requirements

  • Travel required, 5-10% (Industry Conferences, Investigator Meetings, Regulatory Inspections as needed)
  • Assigned occupancy type based on role nature and responsibilities
  • Site-essential roles require 100% of shifts onsite at assigned facility
  • Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at assigned facility
  • 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 essential

Locations

  • Warsaw, United States

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

150,000 - 250,000 USD / yearly

Source: ai estimated

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

Skills Required

  • Communicate effectively with senior management and cross-functional teamsintermediate
  • Solid knowledge of submission requirements (e.g., New Drug Application (NDA)/Biologics License Application (BLA)/Market Authorization Application (MAA))intermediate
  • Solution-oriented mindset and ability to drive changeintermediate
  • Proven time management skillsintermediate
  • Ability to be flexible to meet job demands, manage multiple priorities, and take on new initiatives and improvement effortsintermediate
  • High level of adaptability in dealing with ambiguous and complex work environmentintermediate
  • Ability to balance multiple demands on role in a responsive and professional mannerintermediate
  • Ability to sustain high levels of performance in a constantly changing environmentintermediate
  • Sound knowledge of Clinical Drug Development Process, regulatory and ICH guidelines (e.g., EMEA, FDA), and industry standard practices regarding data managementintermediate
  • Demonstrated knowledge of Microsoft Office skillsintermediate
  • Well versed in industry trends and emerging technologies supporting data collectionintermediate
  • Strong project managementintermediate
  • Exhibits expertise in metrics analysis and reporting methodologiesintermediate

Required Qualifications

  • Bachelor's Degree required (experience)
  • Minimum 6 years of relevant industry experience (experience)
  • Strong line management experience (experience)

Preferred Qualifications

  • Advanced degree preferred (experience)
  • Strong experience in program governance in all phases of clinical trials for Clinical Data Management delivery (experience)
  • Strong experience in managing Clinical Data Review teams across therapeutic areas (experience)
  • Strong knowledge and experience of EDC systems (Medidata RAVE preferred) (experience)

Responsibilities

  • Line management responsibility of Data Management Data Review staff
  • Manage resource assignments to ensure appropriate support for data quality oversight in clinical trials
  • Forecast future resource needs based on the book of work and initiatives
  • Propose solutions to meet potential resource constraints
  • Assign resources to initiatives in line with their development plans
  • Provide appropriate guidance to staff to influence results and drive to completion
  • Work proactively with staff to understand individual strengths, opportunities, and career goals
  • Support development of plans that capitalize on strengths and address opportunities
  • Provide regular feedback to promote development
  • Effectively coach and mentor staff, seeking out training opportunities where needed
  • Develop and promote a workplace culture that values diversity of thought, promotes integrity, creates accountability, supports effective decision making, and provides opportunities to grow
  • Use clear communications and collaborative strategies to drive to resolution
  • Author procedural documents (SOPs, work instructions, job aids) and coordinate reviews/approvals
  • Ensure procedural documents are reflective of industry standards and regulatory requirements, include optimal processes, and are regularly maintained
  • Work collaboratively on multi-disciplinary project teams and develop productive relationships with external vendors

Benefits

  • general: Uniquely interesting work, life-changing careers
  • general: Supportive culture promoting global participation in clinical trials
  • general: Shared values of passion, innovation, urgency, accountability, inclusion, and integrity
  • general: Opportunity to transform your life and career
  • general: Reasonable workplace accommodations/adjustments for people with disabilities
  • general: Transparent recruitment process
  • general: Ongoing support in roles for people with disabilities

Travel Requirements

0%

Target Your Resume for "Sr Manager, Line Manager, CDM" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Sr Manager, Line Manager, CDM. Takes only 15 seconds!

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

Check Your ATS Score for "Sr Manager, Line Manager, CDM" , 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

Related Jobs You May Like

No related jobs found at the moment.

Bristol-Myers Squibb logo

Sr Manager, Line Manager, CDM

Bristol-Myers Squibb

Sr Manager, Line Manager, CDM

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 24, 2025

Number of Vacancies: 1

Job Description

Manager, Line Manager-Clinical Data Management is a leadership role providing program leadership and potential line management responsibility considered essential to the sustainability and success of the BMS R&D pipeline. Responsibilities will include, but are not limited to: Line Management Line management responsibility of Data Management Data Review staff based on business requirements Manages the resource assignments ensuring appropriate support is in place to provide data quality oversight for clinical trials Forecast's future resource needs based on the book of work and initiatives; proposing solutions to meet potential resource constraints Assigns resources to initiatives in line with their development plans and providing appropriate guidance to staff to influence results and drive to completion Works proactively with staff to understand individual strengths, opportunities, and career goals; supporting development of plans that capitalize on strengths and address opportunities; providing regular feedback to promote development. Effectively coaches and mentors' staff, seeking out training opportunities where needed, to develop the next generation leaders. Develops and promotes a workplace culture that values diversity of thought, promotes integrity, creates accountability, supports effective decision making, and provides opportunities to grow. Using clear communications and collaborative strategies to drive to resolution Authors procedural documents (SOPs, work instructions, job aids) and coordinating reviews/approvals. Ensuring procedural documents are reflective of industry standards and regulatory requirements, include optimal processes and are regularly maintained. Bachelor's Degree required with an advanced degree preferred. Minimal 6 years of relevant industry experience with strong line management experience. Communicate effectively with senior management and crossfunctional teams. Solid knowledge of submission requirements, [e.g. New Drug Application (NDA)/Biologics License Application (BLA)/Market Authorization Application (MAA)] Solution oriented mindset and ability to drive change. Proven time management skills and ability to be flexible to meet job demands, manage multiple priorities, and take on new initiatives and improvement efforts. Demonstrates a high level of adaptability in dealing with ambiguous and complex work environment and balances multiple demands on role in a responsive and professional manner. Ability to sustain high levels of performance in a constantly changing environment. Travel required , 5-10% Industry Conferences, Investigator Meetings, Regulatory Inspections (as needed) 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. Strong experience in program governance in all phases of clinical trials for Clinical Data Management delivery. Strong experience in managing Clinical Data Review teams across therapeutic areas. Able to work collaboratively on multi-disciplinary project teams and develop productive relationships with external vendors. Sound knowledge of Clinical Drug Development Process, regulatory and ICH guidelines (e.g. EMEA, FDA) and industry standard practices regarding data management. Strong knowledge and experience of EDC systems (Medidata RAVE preferred); demonstrated knowledge of Microsoft Office skills and well versed in industry trends and emerging technologies supporting data collection. Strong project management; Exhibits expertise in metrics analysis and reporting methodologies.

About the Role/Company

  • BMS is dedicated to transforming patients' lives through science
  • Every BMS employee plays an integral role in work that goes far beyond ordinary
  • BMS empowers individual talents and unique perspectives in a supportive culture
  • BMS promotes global participation in clinical trials
  • BMS values passion, innovation, urgency, accountability, inclusion, and integrity
  • BMS is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments, and ongoing support in their roles
  • BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws
  • BMS will never request payments, financial information, or social security numbers during the application or recruitment process
  • Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations

Key Responsibilities

  • Line management responsibility of Data Management Data Review staff
  • Manage resource assignments to ensure appropriate support for data quality oversight in clinical trials
  • Forecast future resource needs based on the book of work and initiatives
  • Propose solutions to meet potential resource constraints
  • Assign resources to initiatives in line with their development plans
  • Provide appropriate guidance to staff to influence results and drive to completion
  • Work proactively with staff to understand individual strengths, opportunities, and career goals
  • Support development of plans that capitalize on strengths and address opportunities
  • Provide regular feedback to promote development
  • Effectively coach and mentor staff, seeking out training opportunities where needed
  • Develop and promote a workplace culture that values diversity of thought, promotes integrity, creates accountability, supports effective decision making, and provides opportunities to grow
  • Use clear communications and collaborative strategies to drive to resolution
  • Author procedural documents (SOPs, work instructions, job aids) and coordinate reviews/approvals
  • Ensure procedural documents are reflective of industry standards and regulatory requirements, include optimal processes, and are regularly maintained
  • Work collaboratively on multi-disciplinary project teams and develop productive relationships with external vendors

Required Qualifications

  • Bachelor's Degree required
  • Minimum 6 years of relevant industry experience
  • Strong line management experience

Preferred Qualifications

  • Advanced degree preferred
  • Strong experience in program governance in all phases of clinical trials for Clinical Data Management delivery
  • Strong experience in managing Clinical Data Review teams across therapeutic areas
  • Strong knowledge and experience of EDC systems (Medidata RAVE preferred)

Skills Required

  • Communicate effectively with senior management and cross-functional teams
  • Solid knowledge of submission requirements (e.g., New Drug Application (NDA)/Biologics License Application (BLA)/Market Authorization Application (MAA))
  • Solution-oriented mindset and ability to drive change
  • Proven time management skills
  • Ability to be flexible to meet job demands, manage multiple priorities, and take on new initiatives and improvement efforts
  • High level of adaptability in dealing with ambiguous and complex work environment
  • Ability to balance multiple demands on role in a responsive and professional manner
  • Ability to sustain high levels of performance in a constantly changing environment
  • Sound knowledge of Clinical Drug Development Process, regulatory and ICH guidelines (e.g., EMEA, FDA), and industry standard practices regarding data management
  • Demonstrated knowledge of Microsoft Office skills
  • Well versed in industry trends and emerging technologies supporting data collection
  • Strong project management
  • Exhibits expertise in metrics analysis and reporting methodologies

Benefits & Perks

  • Uniquely interesting work, life-changing careers
  • Supportive culture promoting global participation in clinical trials
  • Shared values of passion, innovation, urgency, accountability, inclusion, and integrity
  • Opportunity to transform your life and career
  • Reasonable workplace accommodations/adjustments for people with disabilities
  • Transparent recruitment process
  • Ongoing support in roles for people with disabilities

Additional Requirements

  • Travel required, 5-10% (Industry Conferences, Investigator Meetings, Regulatory Inspections as needed)
  • Assigned occupancy type based on role nature and responsibilities
  • Site-essential roles require 100% of shifts onsite at assigned facility
  • Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at assigned facility
  • 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 essential

Locations

  • Warsaw, United States

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

150,000 - 250,000 USD / yearly

Source: ai estimated

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

Skills Required

  • Communicate effectively with senior management and cross-functional teamsintermediate
  • Solid knowledge of submission requirements (e.g., New Drug Application (NDA)/Biologics License Application (BLA)/Market Authorization Application (MAA))intermediate
  • Solution-oriented mindset and ability to drive changeintermediate
  • Proven time management skillsintermediate
  • Ability to be flexible to meet job demands, manage multiple priorities, and take on new initiatives and improvement effortsintermediate
  • High level of adaptability in dealing with ambiguous and complex work environmentintermediate
  • Ability to balance multiple demands on role in a responsive and professional mannerintermediate
  • Ability to sustain high levels of performance in a constantly changing environmentintermediate
  • Sound knowledge of Clinical Drug Development Process, regulatory and ICH guidelines (e.g., EMEA, FDA), and industry standard practices regarding data managementintermediate
  • Demonstrated knowledge of Microsoft Office skillsintermediate
  • Well versed in industry trends and emerging technologies supporting data collectionintermediate
  • Strong project managementintermediate
  • Exhibits expertise in metrics analysis and reporting methodologiesintermediate

Required Qualifications

  • Bachelor's Degree required (experience)
  • Minimum 6 years of relevant industry experience (experience)
  • Strong line management experience (experience)

Preferred Qualifications

  • Advanced degree preferred (experience)
  • Strong experience in program governance in all phases of clinical trials for Clinical Data Management delivery (experience)
  • Strong experience in managing Clinical Data Review teams across therapeutic areas (experience)
  • Strong knowledge and experience of EDC systems (Medidata RAVE preferred) (experience)

Responsibilities

  • Line management responsibility of Data Management Data Review staff
  • Manage resource assignments to ensure appropriate support for data quality oversight in clinical trials
  • Forecast future resource needs based on the book of work and initiatives
  • Propose solutions to meet potential resource constraints
  • Assign resources to initiatives in line with their development plans
  • Provide appropriate guidance to staff to influence results and drive to completion
  • Work proactively with staff to understand individual strengths, opportunities, and career goals
  • Support development of plans that capitalize on strengths and address opportunities
  • Provide regular feedback to promote development
  • Effectively coach and mentor staff, seeking out training opportunities where needed
  • Develop and promote a workplace culture that values diversity of thought, promotes integrity, creates accountability, supports effective decision making, and provides opportunities to grow
  • Use clear communications and collaborative strategies to drive to resolution
  • Author procedural documents (SOPs, work instructions, job aids) and coordinate reviews/approvals
  • Ensure procedural documents are reflective of industry standards and regulatory requirements, include optimal processes, and are regularly maintained
  • Work collaboratively on multi-disciplinary project teams and develop productive relationships with external vendors

Benefits

  • general: Uniquely interesting work, life-changing careers
  • general: Supportive culture promoting global participation in clinical trials
  • general: Shared values of passion, innovation, urgency, accountability, inclusion, and integrity
  • general: Opportunity to transform your life and career
  • general: Reasonable workplace accommodations/adjustments for people with disabilities
  • general: Transparent recruitment process
  • general: Ongoing support in roles for people with disabilities

Travel Requirements

0%

Target Your Resume for "Sr Manager, Line Manager, CDM" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Sr Manager, Line Manager, CDM. Takes only 15 seconds!

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

Check Your ATS Score for "Sr Manager, Line Manager, CDM" , 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

Related Jobs You May Like

No related jobs found at the moment.