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60 Invitae Clinical Data Manager Jobs Hiring Near You

Eliassen Group

Clinical Data Manager

Chicago, IL · On-site +1

$50 - $60/hr

Description Remote The organization seeks a Clinical Data Manager to lead data management activities for a cardiovascular clinical trial. The role will oversee CRO partners, EDC build and validation ...

Katalyst

Clinical Data Manager

Addison, TX · On-site

The Clinical Data Manager is responsible for leading and overseeing all data management activities for assigned projects. This includes the selection and management of external data management ...

MapLight Therapeutics

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

We are seeking a highly skilled and motivated Clinical Data Manager to join our Clinical Data Management team. Reporting to the Associate Director, the Clinical Data Manager, will play a pivotal role ...

Pharmaron

Clinical Data Manager

Somerset, NJ · On-site

$60K - $75K/yr

Clinical Data Manager FLSA Status: Exempt Location: Onsite (Somerset, New Jersey) Salary: $60,000 - $75,000 Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech ...

TalentBurst, Inc.

Clinical Data manager

Durham, NC · On-site

Clinical Data manager Location: Durham, NC 27709 Duration: 9 Months Job Summary: The Clinical Data Manager will apply his or her knowledge of Clinical Research, therapeutic areas and Clinical ...

Ceribell, Inc

Clinical Data Manager

Sunnyvale, CA · On-site

$190K - $200K/yr

The Clinical Data Manager is the technical lead for clinical data management, accountable for designing and governing end-to-end data strategies to ensure high quality, clinical data across multiple ...

Belcan

Clinical Data Manager

Durham, NC · On-site

$55 - $65/hr

Clinical Data Manager Location: Durham, NC Duration: 09 Months contract(Potential temp to Perm) Payrate: $55/hr. - $65/hr. (Depending on experience) Shift: 1st shift, Mon-Fri , 8am-4:30pm Start Date:

TalentBurst

Clinical Data manager

Durham, NC

Clinical Data manager Location: Durham, NC 27709 Duration: 9 Months Job Summary: The Clinical Data Manager will apply his or her knowledge of Clinical Research, therapeutic areas and Clinical ...

Pharmaron

Clinical Data Manager

Somerset, NJ

$60K - $75K/yr

Clinical Data Manager FLSA Status: Exempt Location: Onsite (Somerset, New Jersey) Salary: $60,000 - $75,000 Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech ...

Pharmaron

Clinical Data Manager

Somerset, NJ · On-site

$60K - $75K/yr

Clinical Data Manager FLSA Status: Exempt Location: Onsite (Somerset, New Jersey) Salary: $60,000 - $75,000 Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech ...

TalentBurst

Clinical Data manager

Durham, NC · On-site

Clinical Data manager Location: Durham, NC 27709 Duration: 9 Months Job Summary: The Clinical Data Manager will apply his or her knowledge of Clinical Research, therapeutic areas and Clinical ...

ImmunityBio

Clinical Data Manager

Culver City, CA · On-site +1

Position Summary The Clinical Data Manager is an expert in clinical data management with demonstrated capability in building and maintaining clinical trial databases. They contribute to process ...

ImmunityBio, Inc.

Clinical Data Manager

Position Summary The Clinical Data Manager is an expert in clinical data management with demonstrated capability in building and maintaining clinical trial databases. They contribute to process ...

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Invitae Jobs Information

What are the key skills and qualifications needed to thrive as a Clinical Data Manager, and why are they important?

To thrive as a Clinical Data Manager, you need a solid understanding of clinical research processes, data management principles, and a degree in life sciences, computer science, or related fields. Expertise with clinical data management systems (CDMS), electronic data capture (EDC) tools, and familiarity with regulatory standards like CDISC and GCP are typically required. Attention to detail, problem-solving abilities, and effective communication distinguish top performers in this role. These skills ensure accurate, compliant data handling and seamless collaboration across clinical research teams, which are critical for successful clinical trial outcomes.

What are some common challenges Clinical Data Managers face when working on multi-site clinical trials?

Clinical Data Managers often encounter challenges such as ensuring data consistency across different sites, managing large volumes of complex data, and coordinating with site staff to resolve discrepancies. They must also stay up-to-date with regulatory requirements and ensure timely data cleaning and database lock. Effective communication and strong organizational skills are essential to navigate these complexities and maintain high data quality throughout the study.

What does a Clinical Data Manager do?

A Clinical Data Manager is responsible for collecting, validating, and managing data from clinical trials to ensure its accuracy, integrity, and compliance with regulatory standards. They design data collection systems, oversee database development, and collaborate with clinical research teams to resolve data discrepancies. By ensuring high-quality data, Clinical Data Managers play a vital role in the success of clinical trials and the development of new medical treatments.

What is it like to work at Invitae?

Invitae is a company that prioritizes collaboration, innovation, and a patient-centric approach to genetic testing and diagnostics. The company's structure is organized into multidisciplinary teams that work together to develop and improve genetic testing products, with a focus on creating a supportive and inclusive work environment. Working at Invitae may appeal to candidates who are passionate about advancing genetic medicine and are interested in contributing to a mission-driven organization that aims to improve human health.
What other companies are hiring for Clinical Data Manager jobs?
Clinical Data Manager

Clinical Data Manager

Katalyst Healthcares & Life Sciences

Addison, TX

Other

Posted 3 days ago

Job description

Job Description:
The Clinical Data Manager is responsible for leading and overseeing all data management activities for assigned projects. This includes the selection and management of external data management vendors, supervision of vendor-delivered tasks, and ensuring the integrity, accuracy, and quality of clinical and operational data. The role also involves close collaboration with internal cross-functional teams to establish and maintain global data standards, support data governance initiatives, and ensure compliance with departmental procedures and regulatory requirements.
Responsibilities:
  • Independently perform Study Data Management activities, ensuring timely and high-quality data delivery.
  • Support Project Data Management Lead (PDML) activities under the guidance of senior leadership, contributing to multi-study or global programs.
  • Oversee and manage all data management activities performed by external vendors, including CRF and database design, Data Management Plan development, data review guidelines, edit specifications, database lock, including SAE reconciliation, external data reconciliation, and dictionary term reconciliation.
  • Review deliverables to ensure adherence to project timelines, data quality standards, and compliance requirements.
  • Conduct data risk assessments and design proactive data quality strategies to mitigate risks throughout the study lifecycle.
  • Ensure that clinical data is collected, cleaned, and formatted according to applicable standards for analysis, reporting, and regulatory submissions.
  • Ensure final datasets meet submission readiness and compliance standards.
  • Track key data management metrics and timelines; communicate progress and risks to cross-functional teams and project management to ensure KPIs are met.
  • Collaborate with internal teams and partner companies to gather and verify trial data for submission; propose alternatives when data gaps are identified.
  • Collaborate with cross-functional teams (Clinical Operations, Biostatistics, Medical Monitoring, etc.) to ensure alignment and efficiency in data management processes.
  • Interface with internal stakeholders and external partners on protocol review, CRF logic and consistency, clinical study reports (CSRs), and statistical analysis plans (SAPs).
  • Participate in discussions with global teams, including regular engagement with Japanese headquarters regarding global data management procedures, standards, and strategy.
  • Monitor industry trends in data management and contribute to the continuous improvement of processes and tools.
  • Review and approve appropriate dictionary versions (e.g., MedDRA, WHO Drug).
  • Archival of end-of-study documents as appropriate.
Requirements:
  • Bachelor's degree in data management, Life Science, Technology, Engineering, Mathematics or a related field is required. An advanced degree (e.g., Master's in Related disciplines) is highly preferred.
  • Minimum of five (5) years of experience in clinical data management within the pharmaceutical, biotechnology, or CRO is required.
  • At least two (2) years of experience in a lead role overseeing study-level data management activities, including vendor oversight and cross-functional collaboration.
  • Proven experience with CRO/vendor management, including performance tracking, and deliverable review.
  • Hands-on experience supporting or leading database lock activities, query management, data reconciliation, SAE handling, and external data integration.
  • Deep understanding of clinical data management principles and regulatory requirements, including ICH-GCP, 21 CFR Part 11, and data privacy regulations (e.g., GDPR, HIPAA), and their connection to data quality, integrity, and audit readiness.
  • Strong understanding of Risk-Based Quality Management (RBQM) principles and their application in data management workflows.
  • Proficient in clinical trial data standards, including CDISC CDASH and SDTM, and practical application in study design and submission deliverables.
  • Solid working knowledge of medical coding dictionaries, such as MedDRA and WHO Drug, including code review, consistency checks, and upgrades.
  • Demonstrated expertise in Electronic Data Capture (EDC) systems, particularly Medidata Rave; working knowledge of other EDC platforms (e.g., Oracle InForm, Veeva) is a plus.
  • Proficient in clinical data systems and tools, such as data visualization/reporting platforms, and tools for data reconciliation.
  • Familiarity with Computerized System Validation (CSV) processes and regulatory expectations.
  • Strong proficiency in Microsoft Office applications (Excel, Word, PowerPoint, Outlook) with the ability to generate reports, dashboards, and presentations for various stakeholders.
  • Basic knowledge of Decentralized Clinical Trials (DCT) models and emerging technologies such as Artificial Intelligence (AI) in the context of data management.
  • Excellent written, oral communication and presentation skills.
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About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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