Clinical Trial Manager, Home based Romania

🔥 0 minutes ago

🇷🇴 Romania – Remote

⏰ Full Time

🟡 Mid-level

🟠 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.

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Develop, coordinate, and implement Phase 1 through Phase 4 clinical research studies • Collaborate with principal investigators, research subjects, client teams, investigators, and clinic operations teams • Plan logistics and resource usage • Track study progress against milestones, deliverables, budgets, and applicable regulations • Oversee site management, clinical monitoring, and central monitoring deliverables • Oversee site interactions from activation through closeout, including recruitment and investigator payments • Identify clinical trial risks and implement mitigations • Review scope of work, budgets, protocols, and contractual obligations • Escalate timeline, quality, budget, and out-of-scope risks to the project manager • Participate in key meetings, including Kick Off Meetings • Serve as an escalation point for investigator site communications • Coordinate with Study Start Up, Patient Recruitment, Data Management, and other functional leaders • Develop and maintain clinical study tools and templates, including Clinical Monitoring Plans • Ensure CTMS, dashboards, and other systems are configured and available, including UAT • Coordinate study-team training on protocols, CRFs, dashboards, SOPs, plans, and timelines • Oversee CRA and Central Monitor resourcing, assignments, conduct, and delivery risks • Review monitoring documentation and ensure quality, compliance, and timely delivery • Provide status updates and solutions to clients, project management, and leadership • Support inspection readiness, corrective action plans, data cuts, and database lock deadlines • Provide performance feedback to line managers

🎯 Requirements

• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience • Demonstrated ability to lead and align teams in the achievement of project milestones • Demonstrated capability of working in an international environment • Demonstrated expertise in site management and monitoring (clinical or central) • Preferred experience with risk-based monitoring • Understanding of clinical trial management financial principles and budget management • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements • Good computer skills • Good communication, presentation and interpersonal skills among project team and with sites • Strong conflict resolution skills • Ability to apply problem-solving techniques to resolve complex issues and apply a risk management approach • Critical thinking to determine causes and appropriate solutions • Approximately 20% travel may be required

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Moderate travel may be required, approximately 20%