Clinical Data Manager at WEP Clinical
Remote, British Columbia, Canada -
Full Time


Start Date

Immediate

Expiry Date

05 Dec, 25

Salary

0.0

Posted On

06 Sep, 25

Experience

15 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

Are you looking for an exciting and fulfilling new position? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring forward ideas that make a real difference. Be part of a mission-driven organization dedicated to advancing clinical research and transforming lives.

Responsibilities

ROLE OBJECTIVES:

The WEP Clinical Data Manager leads and oversees the data management activities for multiple clinical trials, ensuring high-quality data and compliance with regulatory requirements. This role involves the management of the design, development, and validation of clinical databases, maintaining robust relationships with external vendors, and actively communicating with Sponsors. As a Clinical Data Manager, you will ensure that all data management processes adhere to regulatory guidelines and prepare the team for audits and inspections, while also engaging directly with customers to align data management strategies with client needs and expectations.

WHAT YOU’LL DO:

  • Lead comprehensive data management activities for multiple clinical trials, ensuring regulatory compliance and data quality.
  • Plan, develop, test, and validate clinical databases and EDC systems to meet trial needs.
  • Collaborate with clients and cross-functional teams on study design, eCRF design, and data cleaning.
  • Monitor and ensure data quality, accuracy, and timely database entries from study sites.
  • Manage external vendors to deliver quality services within project timelines.
  • Maintain regular communication with clients to update on milestones and progress.
  • Ensure adherence to GCP, ICH, and regulatory requirements, supporting audits and inspections.
  • Proactively track study timelines, managing risks and deviations effectively.
  • Contribute to process improvement by developing systems, SOPs, and guidance documents.
  • Support business development activities, including preparing presentations and bid defense materials.
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