Remote Senior Clinical Data Manager

Placements24

United States

Remote

USD 120,000 - 180,000

Full time

34 hours ago
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Benefits offered by this job

Health insurance
Performance bonuses
Home office stipend
Retirement savings contributions
Remote-first culture

Job summary

Placements24 is seeking a Remote Senior Clinical Data Manager to lead clinical data management for global trials. You will develop data management plans, establish data collection standards, and ensure regulatory compliance from a home office.

The ideal candidate has 7+ years in CDM within pharma/biotech/CRO, strong leadership, and expertise in EDC systems (Medidata Rave, Oracle Clinical, Veeva). This fully remote role supports global programs and remote collaboration.

Qualifications

  • Bachelor's degree in a scientific, healthcare, or related field.
  • Master's degree is a plus and preferred for seniority.
  • Minimum of 7 years of progressive experience in clinical data management in pharma/biotech/CRO.
  • Extensive experience with EDC systems (Medidata Rave, Oracle Clinical, Veeva EDC).
  • Thorough understanding of clinical trial processes, data management lifecycles, GCP, and ICH guidelines.
  • Proven leadership of data management activities for Phase I–IV trials.
  • Strong project management skills and ability to manage multiple projects.
  • Excellent analytical and problem-solving abilities with attention to detail.
  • Proficiency in CDISC standards (SDTM, ADaM).
  • Exceptional written and verbal communication; ability to work with internal teams and external partners.
  • Demonstrated ability to lead a remote team.

Responsibilities

  • Develop and implement Clinical Data Management Plans (CDMPs) for assigned trials.
  • Oversee design, build, and validation of databases using EDC systems (Medidata Rave, Oracle Clinical).
  • Manage data collection, cleaning, and validation per protocol and regulatory standards.
  • Oversee data queries to ensure high-quality datasets.
  • Lead and mentor a team of CDMs and Data Coordinators.
  • Develop and maintain data standards, dictionaries, and SOPs for data management activities.
  • Ensure compliance with GCP, ICH guidelines, and regulatory requirements.
  • Collaborate with clinical operations, biostatistics, programming, and medical teams on data strategies.
  • Participate in and lead data management review meetings; present data status and progress.
  • Manage timelines and resources for data management activities; ensure timely database lock.
  • Contribute to process and technology improvements in data management.

Skills

Clinical Data Management
GCP & ICH
Project Management
Leadership & Mentoring
Remote Team Leadership
CDISC (SDTM/ADaM)
Regulatory Compliance
Data Quality & Integrity
Strong Communication

Education

Bachelor's degree in a scientific/healthcare field
Master's degree preferred

Tools

Medidata Rave
Oracle Clinical
Veeva EDC

Job description

About the Role

Our client, a rapidly expanding pharmaceutical research organization, is seeking an experienced Remote Senior Clinical Data Manager to lead and oversee all aspects of clinical data management for global clinical trials. This fully remote position offers the unique opportunity to manage data integrity and quality from the comfort of your home office. You will be responsible for developing data management plans, establishing data collection standards, and ensuring compliance with regulatory requirements. The ideal candidate is a highly organized, detail-oriented professional with a proven track record in clinical data management within the pharmaceutical or biotechnology sectors. This remote role requires strong leadership skills and the ability to effectively manage projects and teams virtually.

Key Responsibilities
  • Develop and implement comprehensive Clinical Data Management Plans (CDMPs) for assigned clinical trials.
  • Oversee the design, build, and validation of clinical databases using EDC systems (e.g., Medidata Rave, Oracle Clinical).
  • Manage data collection, cleaning, and validation processes, ensuring data accuracy, completeness, and consistency according to protocol and regulatory standards.
  • Oversee the generation and resolution of data queries to ensure high-quality data sets.
  • Lead and mentor a team of Clinical Data Managers and Data Coordinators, providing guidance and support.
  • Develop and maintain data standards, dictionaries, and standard operating procedures (SOPs) for data management activities.
  • Ensure compliance with Good Clinical Practice (GCP), ICH guidelines, and other relevant regulatory requirements.
  • Collaborate with clinical operations, biostatistics, programming, and medical teams to ensure alignment on data management strategies.
  • Participate in and lead data management review meetings, presenting data status and progress.
  • Manage timelines and resources for data management activities, ensuring timely database lock.
  • Contribute to the development and improvement of data management processes and technologies.
Requirements
  • A Bachelor's degree in a scientific, healthcare, or related field.
  • A Master's degree is a plus.
  • A minimum of 7 years of progressive experience in clinical data management within the pharmaceutical, biotechnology, or CRO industry.
  • Extensive experience with Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Oracle Clinical, Veeva EDC).
  • Thorough understanding of clinical trial processes, data management lifecycles, GCP, and ICH guidelines.
  • Proven experience in leading data management activities for Phase I-IV clinical trials.
  • Strong project management skills, with the ability to manage multiple projects simultaneously.
  • Excellent analytical and problem-solving abilities with a keen attention to detail.
  • Proficiency in data standards such as CDISC (SDTM, ADaM).
  • Exceptional written and verbal communication skills, with the ability to effectively communicate with internal teams and external partners.
  • Demonstrated ability to work independently and manage a remote team effectively.
Benefits

Our client offers a highly competitive salary, a comprehensive benefits package including excellent health insurance, retirement savings contributions, and performance-driven bonuses. This role provides the ultimate flexibility of a fully remote work environment, supported by a home office stipend. You will have significant opportunities for career advancement and professional development. Join a dynamic and growing organization committed to accelerating medical breakthroughs and fostering a collaborative, remote-first culture.

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