Senior Clinical Research Associate, 0.5 FTE

🔥 1 hour ago

🇧🇪 Belgium – Remote

⏱ Part Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Ensure compliance with study protocols, ICH-GCP guidelines, regulatory requirements, and company procedures across assigned sites • Evaluate site performance, recommend site-specific actions, escalate significant issues, and support corrective action plans • Verify informed consent processes are appropriately conducted and documented • Assess patient safety and clinical data integrity, including protocol deviations, violations, pharmacovigilance concerns, and site-level risks • Conduct remote and on-site monitoring according to the Clinical Monitoring Plan and Study Monitoring Plan • Perform source document review and verification of clinical data entered into case report forms • Manage protocol deviation reporting, follow-up activities, and resolution of data queries • Review investigational product accountability, storage, security, dispensing, administration, reconciliation, and documentation • Document monitoring findings and study activities through monitoring reports, follow-up letters, communication logs, and required study documentation • Ensure appropriately trained and delegated site personnel perform study activities • Maintain tracking of observations, action items, site status, and study progress in required systems • Review essential study records to maintain inspection readiness • Participate in investigator, sponsor, monitoring, and project team meetings • Collaborate with the primary Site Manager and stakeholders to support study objectives, deliverables, and timelines

🎯 Requirements

• Bachelor's degree, Registered Nurse (RN), or an equivalent combination of education, training, and experience • Experience in clinical research monitoring with oncology trial experience and knowledge of RECIST criteria • Knowledge of ICH-GCP, applicable regulatory requirements, and clinical trial processes • Experience conducting on-site and remote monitoring activities • Strong verbal and written communication, presentation, organizational, and interpersonal skills • Ability to build and maintain effective relationships with investigator site personnel and study stakeholders • Proficiency in the local language • Advanced-level or fluent English language skills • Experience working within sponsor-dedicated clinical research environments preferred

🏖️ Benefits

• Part-time 0.5 FTE schedule • Remote/home-based capacity • Continuous learning and professional development • Flexible work environment • Growth opportunities • Meaningful impact on clinical research and patient care