Experimented CRA in Oncology - single sponsor - Based in Paris Area (Home Based)
CRA with on-site and remote monitoring experience ensuring GCP compliance and trial quality.
- Remote
- Full Time
- Min. 2 YOE
Syneos Health
585 open rolesLast updated May 5, 2026 at 8:33 AM UTC
All open jobs at Syneos Health
Browse the full live job inventory for Syneos Health. This page is focused on current openings, while the overview tab highlights role groups and hiring patterns.
585 open positions
Director, Tech Customer Success - Client Tech Solutions
Lead teams of Managers and Customer Success Analysts to drive technology-driven value and strategic customer success initiatives.
Remote • United States- Full Time
- Min. 5 YOE
CRA II - Sponsor Dedicated (Home-Based - FL / GA)
Monitors clinical sites ensuring regulatory compliance, data integrity, and timely issue resolution across remote US sites.
- Remote • United States
- Full Time
- $70,100 – $126,100/year
West Coast Regional Leader, Business Development
Lead regional business development efforts in West Coast, targeting pharmaceutical partners and accelerating growth.
- Remote • United States
- Full Time
- $193,600 – $367,800/year
Senior Clinical Data Scientist (Lead Data Management) - Poland, Hungary or Romania - hybrid
Senior clinical data scientist leads data management activities and ensures data quality across studies in Central Europe.
- Full Time
Clinical Project Manager II – Biomarker Study Management (Sponsor-Dedicated | Remote)
Lead biomarker study operations and cross-functional trial delivery for sponsor-dedicated, remote role in biomarker study management.
- Remote • California, USA
- Full Time
Sr. Technical Project Manager
Lead cross-functional initiatives to deliver technical projects in a hybrid Buenos Aires setting.
Hybrid • Buenos Aires, Argentina- Full Time
Principal Clinical Trial Regulatory Affairs - LATAM
Clinical regulatory affairs expert with LATAM submissions to lead strategy and coordination for trial approvals.
- Full Time
- Min. 4 YOE
Sr. CRA II (Site reviewing / report reviewing )
(7+ years) Onsite clinical monitoring with strong oncology experience and site activation responsibilities.
Remote • India- Full Time
- Min. 7 YOE
CTM I / CTM II
Clinical trial management roles overseeing site monitoring, risks and data integrity with CTMS tooling and vendor management.
- Remote • India
- Full Time
- Min. 2 YOE
Pr Statistical Programmer
Statistical programmer leveraging SAS to develop datasets, tables and outputs per SAP, leading programming activities and cross-functional coordination.
- Remote • India
- Full Time
- Min. 8 YOE
Sr CRA I Barcelona. Sponsor dedicated
Clinical research professional performing site qualification/monitoring with remote-capable duties and sponsors collaboration.
Remote • Spain- Full Time
- Min. 3 YOE
Data Engineer I -Hyderabad (Hybrid)
Develop and optimize data pipelines to address specific business needs with cross-functional collaboration.
- Hybrid • Hyderabad, Telangana, India
- Full Time
- Min. 2 YOE
Director, Safety and PV Systems (Innovation & AI)
Lead end-to-end SPVG technology solutions including AI/ML prototypes and PV systems, balancing speed, compliance, and value.
- Remote • Madrid, Spain
- Full Time
CRA II / Sr. CRA I (Oncology)
Oncology monitoring specialist with 5+ years’ experience and GCP expertise.
- Remote
- Full Time
- Min. 5 YOE
Sr. CRA I
Site monitoring and management professional performing ICH-GCP compliant visits, overseeing trial sites and data integrity.
- Remote
- Full Time
- Min. 1 YOE
Sr CRA Ukraine
Clinical monitoring professional supporting site qualification, initiation and monitoring across trials with remote/onsite coordination.
Remote • Ukraine- Full Time
Stat Programmer II/ Sr Statistical Programmer (R/R Shiny)
Hands-on R statistics and Shiny development for clinical data visualization and trial support, with version control and tidyverse expertise.
- Remote • India
- Full Time
- Min. 5 YOE
Sr Clinical Research Associate - Central/West Coast
Clinical monitoring and site management role ensuring GCP compliance with on-site or remote visits.
- Remote • United States
- Full Time
Manager, Clinical Data/Medical Science (Remote - NA only)
Role leads clinical data/medical science team delivering compliant, high-quality clinical research services for US/Canada markets.
- Full Time
- Min. 5 YOE
Senior Site Activation Specialist
Senior Site Activation Specialist responsible for country-level site activation submissions, regulatory coordination, and end-to-end SSU processes.
- Remote • Australia/Oceania
- Full Time
Pr. Statistical Programmer (Clinical Pharmacology)
Senior statistical programmer role developing and validating SAS-based outputs for clinical pharmacology; leads programming activities and CDISC/CDISC standards compliance.
- Remote • Hyderabad, Telangana, India
- Full Time
- Min. 5 YOE
Senior Statistical Programmer (Clinical Pharmacology)
Senior Statistical Programmer role focusing on SAS programming for SDTM/ADaM in clinical trials.
- Remote
- Full Time
- Min. 5 YOE
SAS I (Due Diligence Specialist) assigned to client Home Based Mexico
Perform start-up activities for investigative sites in clinical trials across assigned country/locations.
Remote • Mexico- Full Time
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