Jobs / United States / Edetek

Manager Clinical Data Management

Edetek · 🇺🇸 Remote · Remote

Sponsorship verdict

No sponsorship evidence yet

No government record and no wording either way. Not a refusal — ask the recruiter.

  • No government sponsor record hereThis employer posted directly and does not match a government sponsor register.
  • The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
  • No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
  • What Edetek paid sponsored hires in similar roles1 certified filing for “Senior Clinical Data Manager” (Data Scientists) in TX: $119k–$119k, median $119k. Most were filed at wage level III (100%) — 3 lottery entries, ≈46% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
  • Confirmed live todayWhen a source last listed this job as open.

US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).

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Sponsorship unknown

No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.

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Sponsor Radar — Edetek

Employer-posted — not on a register

This employer posted directly and does not match a government sponsor register.

Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Edetek →

About the role

Manager, Clinical Data Management leads clinical data management team to handle project management documentation, preform clinical data management activities and system implementations for EDETEK’s CONFORM eClinical, write design specifications for the system (forms, reports, etc.), and facilitate testing of system implementations. In addition to stay hands-on with clinical data management operations and activities, Manager of Clinical Data Management oversees data management projects to ensure quality, timely delivery and ongoing client satisfaction; identifies client needs and develops creative solutions for projects, leveraging expertise, operational capabilities and technologies; communicates with clients and internal teams. The Manager, Clinical Data Management should thoroughly understand the requirements for Good Clinical Data Management services, including its documentation; be involved in start-up or wrap-up of in-house and client-specific data management projects; have an understanding of the relevant therapeutic indications, study hypotheses, and trial design; and have a solid understanding of database design and structure. ESSENTIAL FUNCTIONS • Support internal clinical data management initiatives • Complete traditional and assigned data management operations/activities • Contribute to project success by communicating with clients about requirements and issues, leveraging expertise, enforcing standard operation procedures, monitoring project progress and timelines. • Assist in the development and maintenance of systems used to support project infrastructure • Work with Clinical Data Specialists (CDSs) to execute Data Management Plans • Lead the communication with clients/sponsors as necessary to deliver contracted clinical data management services and clinical data with high quality and integrity • Ensure filing of all required documentation per EDETEK and project requirements • Lead Use Acceptance Testing (UAT) on new software • Select and interview clinical data manager candidates • Train and guide junior team members • Ability to communicate effectively in the English language in person, by phone and in writing. • Ability to lead functional meetings • Strong attention to detail and accuracy is a must • Excellent organizational skills • Demonstrated ability to manage multiple projects • Ability to work collaboratively, effectively, and productively in diverse organization structures. • Ability to work independently, take initiative and complete tasks to deadlines: Delivering Excellence, Serving Customers, Accountability and Ownership, Global and Cross-Functional Communication • Ability to work in a team-oriented, collaborative environment. • Ability to work positively within a continually changing environment. • Ability to effectively prioritize and execute tasks in a high-pressure environment. • Advanced computer skills and practical knowledge of MS Office and potentially project management software. • A Bachelor’s degree or equivalent combination of Education/Training/Experience is required. A degree in a scientific, medical, or technological discipline is preferred. • A minimum of 2 years of clinical trial or clinical data management experience or similar industry experience/training is required. • Prior trial responsibility for the entire data management life-cycle is desirable. • Working knowledge of EDC studies and SAS is required. • Corporate office environment. • Some travel (5%) may be required with a potential of travel occurring over weekends. • Cross-functional interactions Benefits vary by country, but remain competitive. Below is a sample of the benefits offered to U.S. employees. • Choice of comprehensive Medical, Vision and Dental Insurance plans • Paid vacation time

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Source: RemoteOK feed First seen: 2026-10-11 Last confirmed: 2026-10-11 How our data works → Report this job

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