Clinical Scientific Liaison – MD or Pharmacist, 5 years experience, Biotech/Pharma, Oncology

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🔥 0 minutes ago

🇦🇷 Argentina – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

💊 Pharmacist

👻 Ghost score 10%

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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

• Provide site management oversight, clinical monitoring and central monitoring deliverables focused on patient safety, protocol/GCP/regulatory compliance and data integrity • Oversee site interactions from activation through closeout, including recruitment, investigator payments and related activities • Identify clinical trial management risks and propose or implement mitigations • Review study scope, budget and protocol content; ensure clinical project teams understand contractual obligations and parameters • Escalate risks affecting timelines, quality, budget or contracted scope • Participate in and present at key meetings, including Kick Off Meetings • Serve as an escalation point for investigator site staff and interact with principal investigators and site staff • Collaborate with Study Start Up, Patient Recruitment, Data Management and other functional leaders to meet study milestones • Develop and maintain clinical study tools and templates, including the Clinical Monitoring Plan • Ensure CTMS, dashboards and other systems are configured and available; oversee UAT and audit-trail reviews • Coordinate protocol-specific and systems training for study teams • Oversee CRA and Central Monitor resourcing, site assignments, conduct and delivery risks • Ensure quality and visibility of clinical monitoring, central monitoring and site management deliverables • Review oversight dashboards and clinical trial systems, including CTMS, EDC, eDiary, ePRO, TMF, IVRS/IWRS and central monitoring dashboards • Ensure team compliance with monitoring strategies, CMP/SMP and risk plans • Review site and central monitoring documentation and ensure timely revisions, approvals and delivery • Provide status updates on clinical deliverables and risks to clients, project management and leadership • Resolve obstacles in protocol execution and site management • Support inspection readiness, corrective action plans, data cuts and database lock deadlines • Oversee CRAs and Central Monitors, assess compliance and identify emerging risks • Provide staff performance feedback and coach or mentor CTMs • Coordinate clinical activities for larger, more complex trials or portfolios when assigned

🎯 Requirements

• Bachelor’s degree or RN in a related field or equivalent combination of education, training, and experience • 5 years of experience in biotech/pharma, preferably including clinical monitoring, clinical science and/or medical monitoring experience • Oncology experience required • Demonstrated ability to lead and align teams in achievement of project milestones • Capability to work in an international environment • Expertise in site management and clinical or central monitoring • Preferred experience with risk-based monitoring • Understanding of clinical trial management financial principles and budget management • Knowledge of Good Clinical Practice/ICH Guidelines and 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 ability to identify issues, determine causes and appropriate solutions • Moderate travel may be required, approximately 20%

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition and total rewards program • Inclusive culture • Comprehensive resources including emerging technologies, data, science and knowledge sharing • Opportunities for diverse career paths and employment growth