Resume and JobRESUME AND JOB
Bristol-Myers Squibb logo

Assoc Manager, CDM

Bristol-Myers Squibb

Assoc Manager, CDM

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 24, 2025

Number of Vacancies: 1

Job Description

Responsibilities will include, but are not limited to: Study Startup: - Draft EDC build timeline in collaboration with Data Management Lead. - Perform DB build tasks by creating specifications for Database and Edit Checks. - Create test scripts and complete test data entry/UAT for Coding, Site Payment, Safety Gateway. - Collaborate with Data Management Lead and facilitate startup meetings which includes, not limited to, EDC build kick-off, Interactive eCRF Build and IRMs (Interactive Review Meeting) for database and Edit checks. - Create and finalize study documents like Data Quality Management Plan, eCRF completion Instructions, Protocol Data Review Plan (PDRP) post Project Management - Support DML in project management tasks to make sure that study is delivered successfully as per the study timelines with quality. Documentation: - Filing of appropriate documents in eTMF as per eTMF master plan. Bachelor's Degree required. 6 years of experience in managing end to end Clinical Data Management tasks. Able to work on end to end Clinical Data Management tasks. Able to work collaboratively on multi-disciplinary project teams. Strong knowledge of Clinical Drug Development Process, FDA/ICH guidelines and industry standard practices regarding data management. Strong knowledge and experience of EDC systems (Medidata RAVE preferred); Travel Required Yes, 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.

About the Role/Company

  • BMS's vision is 'Transforming patients' lives through science™'
  • Every BMS employee plays an integral role in work that goes far beyond ordinary
  • Employees are empowered to apply individual talents and unique perspectives in a supportive culture
  • BMS is dedicated to ensuring that people with disabilities can excel
  • 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 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

  • Draft EDC build timeline in collaboration with Data Management Lead
  • Perform DB build tasks by creating specifications for Database and Edit Checks
  • Create test scripts and complete test data entry/UAT for Coding, Site Payment, Safety Gateway
  • Collaborate with Data Management Lead and facilitate startup meetings including EDC build kick-off, Interactive eCRF Build and IRMs for database and Edit checks
  • Create and finalize study documents like Data Quality Management Plan, eCRF completion Instructions, Protocol Data Review Plan (PDRP)
  • Support DML in project management tasks to ensure study is delivered successfully as per the study timelines with quality
  • Filing of appropriate documents in eTMF as per eTMF master plan

Required Qualifications

  • Bachelor's Degree
  • years of experience in managing end to end Clinical Data Management tasks

Preferred Qualifications

  • Strong knowledge and experience of EDC systems (Medidata RAVE preferred)

Skills Required

  • Able to work on end to end Clinical Data Management tasks
  • Able to work collaboratively on multi-disciplinary project teams
  • Strong knowledge of Clinical Drug Development Process, FDA/ICH guidelines and industry standard practices regarding data management

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
  • 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% for 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, Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite, Field-based and remote-by-design roles require physical travel to visit customers, patients or business partners and to attend meetings

Locations

  • Warsaw, United States

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

100,000 - 150,000 USD / yearly

Source: ai estimated

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

Skills Required

  • Able to work on end to end Clinical Data Management tasksintermediate
  • Able to work collaboratively on multi-disciplinary project teamsintermediate
  • Strong knowledge of Clinical Drug Development Process, FDA/ICH guidelines and industry standard practices regarding data managementintermediate

Required Qualifications

  • Bachelor's Degree (experience)
  • years of experience in managing end to end Clinical Data Management tasks (experience)

Preferred Qualifications

  • Strong knowledge and experience of EDC systems (Medidata RAVE preferred) (experience)

Responsibilities

  • Draft EDC build timeline in collaboration with Data Management Lead
  • Perform DB build tasks by creating specifications for Database and Edit Checks
  • Create test scripts and complete test data entry/UAT for Coding, Site Payment, Safety Gateway
  • Collaborate with Data Management Lead and facilitate startup meetings including EDC build kick-off, Interactive eCRF Build and IRMs for database and Edit checks
  • Create and finalize study documents like Data Quality Management Plan, eCRF completion Instructions, Protocol Data Review Plan (PDRP)
  • Support DML in project management tasks to ensure study is delivered successfully as per the study timelines with quality
  • Filing of appropriate documents in eTMF as per eTMF master plan

Benefits

  • general: Uniquely interesting work
  • general: Life-changing careers
  • general: Supportive culture promoting global participation in clinical trials
  • general: Shared values of passion, innovation, urgency, accountability, inclusion and integrity
  • 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%

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Tags & Categories

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Bristol-Myers Squibb logo

Assoc Manager, CDM

Bristol-Myers Squibb

Assoc Manager, CDM

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 24, 2025

Number of Vacancies: 1

Job Description

Responsibilities will include, but are not limited to: Study Startup: - Draft EDC build timeline in collaboration with Data Management Lead. - Perform DB build tasks by creating specifications for Database and Edit Checks. - Create test scripts and complete test data entry/UAT for Coding, Site Payment, Safety Gateway. - Collaborate with Data Management Lead and facilitate startup meetings which includes, not limited to, EDC build kick-off, Interactive eCRF Build and IRMs (Interactive Review Meeting) for database and Edit checks. - Create and finalize study documents like Data Quality Management Plan, eCRF completion Instructions, Protocol Data Review Plan (PDRP) post Project Management - Support DML in project management tasks to make sure that study is delivered successfully as per the study timelines with quality. Documentation: - Filing of appropriate documents in eTMF as per eTMF master plan. Bachelor's Degree required. 6 years of experience in managing end to end Clinical Data Management tasks. Able to work on end to end Clinical Data Management tasks. Able to work collaboratively on multi-disciplinary project teams. Strong knowledge of Clinical Drug Development Process, FDA/ICH guidelines and industry standard practices regarding data management. Strong knowledge and experience of EDC systems (Medidata RAVE preferred); Travel Required Yes, 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.

About the Role/Company

  • BMS's vision is 'Transforming patients' lives through science™'
  • Every BMS employee plays an integral role in work that goes far beyond ordinary
  • Employees are empowered to apply individual talents and unique perspectives in a supportive culture
  • BMS is dedicated to ensuring that people with disabilities can excel
  • 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 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

  • Draft EDC build timeline in collaboration with Data Management Lead
  • Perform DB build tasks by creating specifications for Database and Edit Checks
  • Create test scripts and complete test data entry/UAT for Coding, Site Payment, Safety Gateway
  • Collaborate with Data Management Lead and facilitate startup meetings including EDC build kick-off, Interactive eCRF Build and IRMs for database and Edit checks
  • Create and finalize study documents like Data Quality Management Plan, eCRF completion Instructions, Protocol Data Review Plan (PDRP)
  • Support DML in project management tasks to ensure study is delivered successfully as per the study timelines with quality
  • Filing of appropriate documents in eTMF as per eTMF master plan

Required Qualifications

  • Bachelor's Degree
  • years of experience in managing end to end Clinical Data Management tasks

Preferred Qualifications

  • Strong knowledge and experience of EDC systems (Medidata RAVE preferred)

Skills Required

  • Able to work on end to end Clinical Data Management tasks
  • Able to work collaboratively on multi-disciplinary project teams
  • Strong knowledge of Clinical Drug Development Process, FDA/ICH guidelines and industry standard practices regarding data management

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
  • 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% for 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, Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite, Field-based and remote-by-design roles require physical travel to visit customers, patients or business partners and to attend meetings

Locations

  • Warsaw, United States

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

100,000 - 150,000 USD / yearly

Source: ai estimated

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

Skills Required

  • Able to work on end to end Clinical Data Management tasksintermediate
  • Able to work collaboratively on multi-disciplinary project teamsintermediate
  • Strong knowledge of Clinical Drug Development Process, FDA/ICH guidelines and industry standard practices regarding data managementintermediate

Required Qualifications

  • Bachelor's Degree (experience)
  • years of experience in managing end to end Clinical Data Management tasks (experience)

Preferred Qualifications

  • Strong knowledge and experience of EDC systems (Medidata RAVE preferred) (experience)

Responsibilities

  • Draft EDC build timeline in collaboration with Data Management Lead
  • Perform DB build tasks by creating specifications for Database and Edit Checks
  • Create test scripts and complete test data entry/UAT for Coding, Site Payment, Safety Gateway
  • Collaborate with Data Management Lead and facilitate startup meetings including EDC build kick-off, Interactive eCRF Build and IRMs for database and Edit checks
  • Create and finalize study documents like Data Quality Management Plan, eCRF completion Instructions, Protocol Data Review Plan (PDRP)
  • Support DML in project management tasks to ensure study is delivered successfully as per the study timelines with quality
  • Filing of appropriate documents in eTMF as per eTMF master plan

Benefits

  • general: Uniquely interesting work
  • general: Life-changing careers
  • general: Supportive culture promoting global participation in clinical trials
  • general: Shared values of passion, innovation, urgency, accountability, inclusion and integrity
  • 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 "Assoc Manager, CDM" , Bristol-Myers Squibb

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

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

Check Your ATS Score for "Assoc 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

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