
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.
🕒 July 25
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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.
• Manage all aspects of the development, coordination, and implementation of 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, client deliverables, budgets, and applicable regulations • Provide site management oversight, clinical monitoring, and central monitoring deliverables • Oversee site interactions from post-activation through site closeout, including recruitment and investigator payments • Identify clinical trial risks and implement mitigations • Review scope of work, budgets, protocols, and contractual obligations • Escalate risks affecting timelines, quality, budget, or contracted scope • Participate in and present at key meetings • Coordinate handoffs with Study Start Up, Patient Recruitment, and Data Management • Develop and maintain clinical study tools and templates, including Clinical Monitoring Plans • Oversee CTMS, dashboards, systems setup, user acceptance testing, access, and audit trail reviews • Coordinate protocol-specific and study-team training • Oversee CRA and Central Monitor resourcing, assignments, conduct, and delivery risks • Review monitoring documentation and ensure compliance with company and sponsor specifications • 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 • Coach and mentor CTMs as assigned
• 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 • Strong conflict resolution skills • Ability to apply problem-solving techniques to resolve complex issues and use a risk management approach • Critical thinking to determine causes and appropriate solutions • Moderate travel may be required, approximately 20%
• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Reasonable accommodations when appropriate
Apply Now🕒 July 17
Application Scientist supporting customers in Clinical Genomics with VarSome bioinformatic tools from pre-sales to post-sales. Collaborate on customer evaluations and onboarding for optimal use of the platform.
🗣️🇵🇱 Polish Required
🕒 July 16
Clinical Research Associate managing oncology studies and supporting a single client at Parexel in Poland. Responsibilities include site management and mentoring junior CRAs with opportunities for travel and remote work.
🇵🇱 Poland – Remote
💵 zł220k - zł240k / year
💰 Venture Round on 1990-01
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
🕒 July 15
Manager in Data Sciences overseeing data management services and collaborating with internal teams. Responsible for operational efficiency, project deliverables, and team management in Clinical Data Management role.
🕒 June 24
Senior Clinical Research Associate managing clinical trial activities to ensure compliance at ICON. Leading monitoring tasks and collaborating with teams for successful trial execution.
🕒 June 22
Managing clinical site monitoring services for multinational projects. Acting as Lead CRA and liaison between CRAs and project teams.