Source Job

Asia

  • Primary DM contact for assigned clinical project(s) / program(s), ensuring that tasks are performed in a timely manner.
  • Oversee project data entry process including development of data entry guidelines, training, data entry quality and resourcing.
  • Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders.

SAS CDISC

6 jobs similar to Senior Clinical Data Manager

Jobs ranked by similarity.

US

  • Lead end-to-end Clinical Data Management activities for assigned clinical studies.
  • Ensure clinical data are accurate, complete, consistent, and inspection-ready.
  • Drive proactive risk identification, issue escalation, and resolution across study teams and vendors.

Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. They are committed to transforming the future of treatment for autoimmune disease, guided by core values and focused on innovation.

Europe

  • Lead a large clinical study or a series of related studies with minimum guidance.
  • Provide mentoring and training to lower-level Data Management staff assigned to your studies.
  • Develop or lead the development of the Data Management Plan for a clinical study.

Parexel provides Clinical and Consulting solutions to the world’s life sciences industry. They have a global breadth of clinical, regulatory and therapeutic expertise, and a proven track record spanning 40+ years.

$125,000–$175,000/yr
US

  • Lead day-to-day data management activities for assigned clinical trials.
  • Oversee CRO and vendor data management deliverables to ensure timelines, quality, and compliance.
  • Ensure data integrity, consistency, and completeness through ongoing data review and cleaning.

Faeth Therapeutics is a clinical-stage oncology company advancing PIKTOR, a multi-node PI3K/AKT/mTOR inhibitor program. They are a small, focused team where every person has direct impact and are united by a shared commitment to care deeply, create boldly, and never stop learning.

Australia

  • Manage and motivate a team of CRAs to achieve Precision for Medicine’s quality standards.
  • Support the career development of the organization’s Clinical Research Associate (CRA) workforce.
  • Strengthen the quality and productivity of operations within the group.

Precision for Medicine is a Clinical Research Organization with a uniquely integrated offering. They combine novel clinical trial designs, industry-leading operational and medical experts, and advanced biomarker and data analytics solutions.

Europe

  • Perform ongoing clinical data review to ensure data quality, consistency, and completeness.
  • Identify discrepancies and raise/resolve queries in EDC systems.
  • Review patient data including eligibility, medical history, treatment, safety data, and outcomes.

Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. They partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity and anticipate change.

$300,000–$375,000/yr

  • Oversee CRO programming activities, including SDTM, ADaM, TFLs, define.xml, reviewer’s guides, and other clinical study or submission deliverables.
  • Review CRO programming plans, specifications, datasets, outputs, QC documentation, issue logs, and submission packages.
  • Collaborate with Data Management to support data cleaning, external data review, reconciliation, database lock, and data quality activities.

Braveheart Bio is a Bay Area–based biopharmaceutical company pioneering best-in-class therapies for cardiovascular disease. They have a proven leadership team, a strong financial foundation, and a high-value late-stage asset, making it an outstanding opportunity for mission-driven professionals.