Clinical Research Job at Novotech, Belgium | Life Sciences | Apply Online
If you are an experienced clinical trials professional looking to elevate your career within the Benelux region, this full-time position at Novotech is an exceptional opportunity. Based in Belgium, this field-and-office-integrated role places you at the operational forefront of an expanding global Contract Research Organization (CRO). For structured relationship managers searching for a high-impact Clinical Research Job, this position offers total ownership over investigational site performance, compliance auditing, and stakeholder engagement. It serves as an elite launchpad for a long-term Novotech career and stands out as a premier choice for professionals tracking a mid-to-senior level Life Sciences Job in Europe.
- Job Position: Clinical Research Associate – Benelux
- Location: Belgium
About The Company
Novotech is a globally recognized, full-service clinical Contract Research Organization (CRO) that has been at the forefront of drug development and scientific advisory services since 1997. Operating more than 30 offices across Asia-Pacific, the United States, and Europe, Novotech specializes in providing biotechnology and pharmaceutical clients with an accelerated path to market for life-changing therapeutics. The company is highly celebrated for its workplace culture, earning distinctions as an Employer of Choice, Great Place to Work, and Employer of Choice for Gender Equality (EOCGE). Through its employee-centered “NovoLife” flexible benefits framework, Novotech empowers its global workforce with the trust, autonomy, and flexibility required to drive professional satisfaction and maximize client trial results.
Clinical Research Job – Key Responsibilities
As a Clinical Research Associate (CRA), you will serve as the primary site relationship manager and central liaison between clinical investigational sites, Novotech project leaders, and pharmaceutical sponsors.
Your core operational, monitoring, and compliance duties will include:
- Site Relationship Management: Building strong professional partnerships with Principal Investigators (PIs), study coordinators, and pharmacists to ensure smooth, expedited trial operations for this Clinical Research Job.
- Comprehensive Trial Monitoring: Executing on-site and remote monitoring visits in strict accordance with ICH-GCP §5.18 guidelines and study-specific Clinical Monitoring Plans (CMP). This includes managing Site Selection, Site Initiation, Site Monitoring, and Site Close-Out milestones.
- Participant Safety & Rights Audits: Protecting trial participant well-being by performing meticulous Informed Consent Form (ICF) audits, confirming patient eligibility, validating protocol compliance, and evaluating Adverse Events (AEs/SAEs) for prompt sponsor reporting.
- Data Verification & Queries: Verifying that reported clinical trial data are accurate, complete, and fully verifiable from raw source documents, driving prompt resolution of electronic Case Report Form (eCRF) data queries.
- Investigational Product (IP) Accountability: Ensuring all study drugs and biologics are appropriately stored, dispensed, tracked, and reconciled at the site pharmacy level.
- Regulatory & Recruitment Acceleration: Collaborating with internal In-house CRAs and Regulatory Start-Up Associates (RSAs) to prepare essential documents and ethics filings, while driving site-specific recruitment plans to hit enrollment targets for this Life Sciences Job.
Qualifications & Requirements For Clinical Research Job
This intermediate-to-advanced position is tailored for high-performing monitor professionals who demonstrate strong critical thinking and rapid decision-making habits.
- Educational Foundation: A Graduate degree in a clinical, or life sciences-related field. Relevant qualifications in allied healthcare professions will also be fully considered.
- Industry Track Record: At least 2 to 3 years of direct Clinical Research Associate (CRA) monitoring experience within a Contract Research Organization (CRO) or pharmaceutical environment is required to advance your Novotech career.
- Technical Skills: Deep, practical working knowledge of ICH-GCP guidelines, local Benelux clinical trial directives, and global regulatory frameworks. High computer literacy and familiarity with CTMS/eCRF software are required.
- Core Competencies: Exceptional interpersonal and team skills, excellent time-management habits, sharp attention to detail, and a strategic mindset capable of troubleshooting site-level bottlenecks independently.
- Logistics: Regular full-time schedule based in Belgium, requiring regional travel to investigational sites as dictated by the Clinical Monitoring Plan.
In short, the Clinical Research Associate position at Novotech Benelux is a definitive route to transitioning your foundational monitoring experience into a high-visibility, autonomous trial management asset. Securing this role allows you to step away from repetitive data collection and take full clinical ownership over multi-center clinical trials on the cutting edge of biotechnology. If you possess a life sciences background, 2–3 years of verifiable field monitoring experience, and a passion for patient safety, apply today to secure this premier opportunity.
