Clinical Scientist, Late Phase

November 21

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Syneos Health

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Biotechnology • Pharmaceuticals • Healthcare Insurance

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.

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

📋 Description

• Responsible for supporting complex or leading low complexity studies across various SOPs, including tasks related to: 1) protocol and protocol specific training, 2) vendor management, 3) study level planning and oversight, 4) data review, 5) regulatory document, study report and publication preparation and review, 6) overall study execution with a critical focus on consistency, quality, data integrity, safety, and alignment with company processes. • Works in a global environment on studies across all regions including International, Emerging Markets and China. • May represent line in program-wide functions and governance as needed. Contributes to discussions to ensure consistency across products/TA. • Using knowledge of epidemiologic/observational and specific aspects of trials, provides support of operational strategic partner involvement at a program or study level. Identifies issues in a timely manner, leads implementation of solutions, and/or escalates as appropriate. • Provides operational input on tactical implementation of studies.

🎯 Requirements

• BA/BS Degree in life sciences or health related field with 5+ years practical experience or MS/MBA with 3+ years, PharmD/PhD 2 years, MD/DO with 1 year • Industry experience in the Clinical Scientist role or similar capacity • Experience working on multinational teams/studies • Hands-on experience in epidemiology study design, conduct and analysis • Experience in or leading study teams • Experience working independently and collaborating with multiple functional groups within and outside the business line • Demonstrated an ability working across multiple studies for incorporation of consistent medical/scientific concepts in multiple protocols • Strong knowledge of the clinical research process and Good Clinical Practices (GCPs), monitoring, clinical and regulatory operations • Demonstrated independent authorship of study protocols and other study documents • Working knowledge of statistics, data analysis, and data interpretation • Experienced in managing external vendors for clinical and/or epidemiological study(ies) • Fluent in English writing, reading, and speaking and has exceptional written and oral communication and cross-functional collaborative skills.

🏖️ Benefits

• Competitive remuneration package with excellent benefits • Commitment to your development and training, with the opportunity to progress your career within a market leading and innovative organization • Opportunity to work within a successful and rewarding environment