Clinical Scientific Advisor

🕒 May 26

🇺🇸 United States – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

Apply Now

Find Similar Remote Jobs

Receive Emails For Remote Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Syneos Health

WebsiteLinkedInAll Job Openings

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.

📋 Description

• Field‑based scientific role focused on building strong relationships with KOLs and reinforcing scientific messaging • Individual contributor supporting assigned program(s)/assets/indications • Key contributor to the implementation of Global Clinical Development Strategy • Ensures consistency of scientific messaging and protocol execution principles across studies • Develop and maintain credible, compliant relationships with PIs/Sub-Is and key study physicians via high-quality scientific exchange related to assigned clinical studies • Provide protocol scientific support using approved materials and within governance • Reinforce scientific understanding of critical-to-quality protocol elements • Help troubleshoot site-level scientific implementation barriers

🎯 Requirements

• min 2 years of relevant experience • experience in supporting clinical trial activities • Neuroscience/Psychiatry therapeutic area preferred • Advanced scientific/clinical degree preferred (e.g., MD, PharmD, PhD, NP/PA) or equivalent combination of education and relevant clinical research experience • Demonstrated experience in a clinical research/development environment with strong understanding of clinical trial methodology and GCP expectations • Proven ability to engage physicians in scientific dialogue and translate complex protocol/science into practical execution guidance • Strong presentation capabilities • Working familiarity with clinical research/site operations and cross-functional matrix partnering

🏖️ Benefits

• career development and progression • supportive and engaged line management • technical and therapeutic area training • peer recognition and total rewards program