Clinical Trial Coordinator – Sponsor Dedicated

🔥 0 minutes ago

🌲 North Carolina – Remote

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💵 $47k - $79.9k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🦅 H1B Visa Sponsor

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Logo of Syneos Health

Syneos Health

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

• Maintain and coordinate the logistical aspects of clinical projects • Provide overall support to functional leads to ensure successful completion of project deliverables • Support the Project Lead in carrying out contracted services and customer expectations in accordance with executed contracts • Set up, maintain, and close out project files and study information across databases and systems • Maintain and distribute study-specific and financial reports • Lead internal and external meetings as directed by the Project Lead • Prepare and distribute meeting minutes and action items • Follow up with team members on action items through closure • Record and assess Key Performance Indicators and communicate proposed action plans • Prepare and provide status reports to customers • Archive study documents according to applicable guidelines and policies • Serve as a project representative for internal and external audits when needed • Support quality assurance activities, audits, internal review, and resolution of actionable issues • Serve as primary customer contact when the Project Lead is unavailable • Mentor and train Project Specialists

🎯 Requirements

• Some combination of education and experience in life sciences, Medicine, Pharmacy, Nursing, or a related field preferred • Moderate relevant clinical research experience • Understanding of clinical drug development and clinical trial operations • Experience in a therapeutic group preferred • Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements • Strong organizational skills • Ability to perform several tasks simultaneously to meet deadlines • Self-motivation and ability to work independently • High proficiency with Veeva Applications • High proficiency with full MS Office Applications • Strong written and spoken communication, presentation, and interpersonal skills • Ability to inform, influence, convince, and persuade • Ability to travel if necessary preferred, approximately 5% • High level of competence in English language

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition and total rewards program • Company car or car allowance • Medical, Dental and Vision health benefits • 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) • Sick time • Reasonable accommodations, when appropriate

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