Senior Clinical Data Manager - US/UK - Remote jobs in United States
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Worldwide Clinical Trials · 1 day ago

Senior Clinical Data Manager - US/UK - Remote

positionUnited States
timeFull-time
remoteRemote
senioritySenior Level
date5+ years exp

Worldwide Clinical Trials is a global, midsize CRO dedicated to innovative approaches in clinical research. The Senior Clinical Data Manager will lead data management services for complex global projects, ensuring data accuracy and integrity throughout the clinical study process.

Health CarePharmaceutical
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H1B Sponsor Likelynote

Responsibilities

Provide fully independent and autonomous leadership of data management services (start up, conduct and close out) across multiple complex global projects/programs
Ensure appropriate resources are allocated to complete all DM activities on time and budget
Prepare DM trial documentation (DMP, DB Specifications, Edit check specifications, CCGs, DTAs)
Write external vendor reconciliation specifications for programming reconciliation outputs (e.g. Serious Adverse Events, IRT, Central Laboratory)
Monitor project scope, budgets and risks and alert DM Management of any concerns
Liaise with DM Management at regular intervals to discuss progress and any issues outstanding (e.g. during Project Review Meetings)
Collaborate with internal Worldwide departments working on the same project
Participate as necessary in sponsor audits, regulatory authority inspections and other third party meetings

Qualification

Clinical data managementData management best practicesClinical trial processProject oversightAnalytical skillsAttention to detailCommunication skillsInterpersonal skillsProblem solving skills

Required

Excellent attention to detail with outstanding written and verbal communication skills
Strong knowledge of data management best practices & technologies as applied to clinical trials
Excellent communication and interpersonal skills to collaborate with cross-functional internal and external teams
Strong understanding of clinical trial process and protocols documents (protocols, statistical analysis plans, CRFs, study reports) and processes
Strong analytical and problem solving skills
Independent and autonomous project oversight skills
Min of 5 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries

Preferred

Educated to degree level (preferably Life Science)
Nursing qualification
Relevant industry experience

Company

Worldwide Clinical Trials

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Worldwide Clinical Trials is a global CRO that provides preclinical and Phase I-IV clinical development services to pharmaceutical industry.
dateFounded in 1986
location
Morrisville, North Carolina, USA
people-size1001-5000 employees
web-link
https://www.worldwide.com

H1B Sponsorship

Worldwide Clinical Trials has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2024 (1)
2023 (5)
2022 (3)
2021 (2)
2020 (2)

Funding

Current Stage
Late Stage
Total Funding
unknown
2023-08-07Acquired

Leadership Team

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Robyn Greener
Associate Director, Project Management
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Recent News

FierceBiotech
Worldwide Clinical Trials adds Catalyst Clinical to global CRO mixture
2026-01-24
PE Hub
Kohlberg portco Worldwide Clinical Trials to acquire QHP-backed Catalyst Clinical Research
2026-01-22
Clinical Trials Arena
Worldwide Clinical Trials to acquire Catalyst
2026-01-22
Company data provided by crunchbase