Job Overview
Location
DEU-Remote
Job Type
Full-time
Category
HR & Recruiting
Date Posted
May 26, 2026
Full Job Description
š Description
- ā¢ The In-house CRA Germany role supports clinical trial operations by providing centralized assistance to Clinical Research Associates (CRAs) and ensuring protocol and regulatory compliance across investigational sites. This role is critical to maintaining data integrity, site readiness, and timely study execution in alignment with Syneos Healthās mission to accelerate healthcare innovation.
- ā¢ Day-to-day responsibilities include remotely reviewing electronic data capture (EDC) and drug accountability logs, updating study systems (e.g., CTMS), supporting site start-up and close-out activities, tracking patient enrollment, assisting with site communications, performing quality control of eTMF, and serving as a primary backup for CRAs during site visits. The role also involves liaising with study teams, preparing IRB submissions, and supporting quality management activities such as audits and inspections.
- ā¢ Syneos Health is a leading fully-integrated life sciences services organization with over 25,000 colleagues globally, dedicated to accelerating customer success across the drug development and commercialization continuum. The company fosters an inclusive culture, invests in employee development through training and career progression, and is driven by its purpose: āDriven to Deliverā ā shaping solutions that impact patient lives.
- ā¢ In this role, you will deepen your expertise in clinical research operations, gain hands-on experience with global trial management systems, strengthen cross-functional collaboration skills, and contribute to high-impact studies that advance novel therapies. Youāll have opportunities for mentorship, professional growth, and exposure to diverse therapeutic areas within a supportive and innovative environment.
šÆ Requirements
- ā¢ Associates Degree (or equivalent) in life sciences, Medicine, Pharmacy, Nursing, or related field, or equivalent combination of education and experience
- ā¢ Knowledge of Good Clinical Practice (GCP)/ICH guidelines and other applicable regulatory requirements
- ā¢ Minimum of 2-3 years of clinical research experience as Sponsor CTS/CTA or Site Coordinator
- ā¢ Fluency in German and high level of competence in English
- ā¢ Strong organizational skills and ability to manage time and work independently
- ā¢ High proficiency with full MS Office Applications
šļø Benefits
- ā¢ Career development and progression opportunities
- ā¢ Supportive and engaged line management
- ā¢ Technical and therapeutic area training
- ā¢ Peer recognition and total rewards program
- ā¢ Inclusive culture where you can authentically be yourself
- ā¢ Purpose-driven work aligned with āDriven to Deliverā mission
Skills & Technologies
About Syneos Health, Inc.
Syneos Health is a global biopharmaceutical services organization providing clinical and commercial solutions. It integrates clinical development, outsourced commercialization, consulting, and communications services to accelerate the delivery of therapies to market. The company supports pharmaceutical, biotechnology, and medical device clients across all phases of product development and commercialization, operating in North America, Europe, and Asia-Pacific.
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