
10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
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.
🔥 0 minutes ago
🏄 California – Remote
💵 $97.3k - $170.3k / year
⏰ Full Time
🟢 Junior
🧪 Clinical Research
🦅 H1B Visa Sponsor
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10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
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.
• Join our Clinical Surveillance & Training (CST) team as a Clinical Scientist, where you will play a critical role in ensuring endpoint quality, data integrity, and trial success across global clinical programs • Design and deliver scientifically grounded rater training programs to ensure consistent, high-quality endpoint assessment and reduce variability across sites • Perform comprehensive eligibility reviews, providing a second level of scientific oversight to confirm appropriate patient selection and minimize protocol deviations and safety risks • Analyze clinical and endpoint data to identify trends, variability, and potential risks—translating findings into actionable insights that improve study execution • Partner with sponsors and study teams to review protocols and provide expert guidance on endpoint strategy, scale selection, and study design feasibility • Collaborate cross-functionally with clinical operations, medical, and sponsor teams to proactively identify risks and deliver solutions that protect study integrity
• Doctoral level degree relevant to therapeutic area (e.g., for CNS: Clinical Psychology PhD or PsyD or Psychiatry MD) • Moderate to extensive clinical experience with patients in relevant therapeutic areas • Knowledge of psychiatric and neuropsychiatric assessments, including patient reported outcome measures, inferential biostatistics, and medical terminology • Experience with clinical research or pharmaceutical industry • Excellent planning/organizational skills and ability to prioritize and multitask • Proficiency in Microsoft Office Suite, specifically: Word, Excel, and PowerPoint • Ability to thrive in a fast-paced environment • Excellent interpersonal and communication skills, both written and spoken, with an ability to inform, influence, convince, and persuade • Strong presentation skills, with experience presenting in professional settings • Ability to travel as necessary (approximately 20%)
• Health benefits to include Medical, Dental and Vision • Company match 401k • Eligibility to participate in Employee Stock Purchase Plan • Eligibility to earn commissions/bonus based on company and individual performance • Flexible paid time off (PTO) and sick time
Apply Now🔥 6 hours ago
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⏰ Full Time
🟢 Junior
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