Contract Management Specialist | MERKUR GROUP | Hybrid Germany

South KoreaRemoteFull-timeSeniorLeadEnglish RequiredClinical Research

Monitor Roche-sponsored clinical trials for a contract research organization, supporting site compliance, accurate data, complete documentation, and trial progress.

United StatesMinnesotaOhio

$212,800 – $319,200 / year

On-siteFull-timeLeadEnglish RequiredClinical Research

Lead Medtronic’s global clinical evidence strategy for peripheral nerve stimulation therapies throughout the product lifecycle. Oversee premarket and postmarket research supporting scientific, regulatory, reimbursement, and commercial goals.

TaiwanHybridFull-timeJuniorMiddleEnglish RequiredChinese RequiredClinical Research

Support Emerald Clinical’s global early-phase trials across APAC. Coordinate study records, meetings, budgets, vendors, and trial master file activities.

United KingdomRemoteFull-timeSeniorEnglish RequiredClinical Research

Use R and Shiny to explore clinical trial data and build interactive visualizations. Support Syneos Health’s life sciences clients with reproducible analyses and insights for clinical decisions.

United StatesCalifornia

$171,000 – $189,000 / year

RemoteFull-timeSeniorEnglish RequiredClinical Research

Lead global clinical operations for Atrium Therapeutics’ RNA therapies targeting cardiomyopathies. Oversee CROs, vendors, budgets, timelines, compliance, and trial delivery.

IsraelRemoteFull-timeJuniorMiddleEnglish RequiredHebrew RequiredClinical Research

Monitor clinical trial sites across Israel for Thermo Fisher Scientific’s PPD services, supporting protocol compliance, data quality, documentation, and audit readiness.

IndiaRemoteFull-timeLeadEnglish RequiredClinical Research

Join Syneos Health’s Clinical Solutions team as a Principal Biostatistician, supporting life sciences and clinical development services. Use biostatistical and drug development expertise to help customers advance drug development and commercialization.

United KingdomIrelandPolandSouth AfricaRemoteFull-timeSeniorEnglish RequiredClinical Research

Lead clinical data standards, quality, and governance for ICON’s sponsor-dedicated trials. Improve global processes and coordinate delivery across teams.

United StatesFloridaKansasNew JerseyNorth CarolinaUtah

$74,500 – $197,500 / year

On-siteFull-timeJuniorMiddleNo degree requiredEnglish RequiredClinical Research

Monitor clinical trial sites and support protocol compliance, patient recruitment, and study documentation for IQVIA. Coordinate with site staff and project teams to help trials meet quality standards and milestones.

United StatesMassachusettsNew JerseyNew York

$93,900 – $153,300 / year

HybridFull-timeJuniorMiddleEnglish RequiredClinical SpecialistGeneral

Support Regeneron clinical trial teams by coordinating study data, sites, reporting, and close-out activities. Help keep studies on track from site activation through completion.