2 days ago
🇺🇸 United States – Remote
💵 $113.9k - $170.9k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
🧪 Clinical Research
🗽 H1B Visa Sponsor
• Serves as the clinical trial lead responsible for the planning, conduct and oversight of the operational portion of clinical studies • Ensures that clinical studies are conducted in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP and all applicable regulatory requirements • Primary clinical point of contact with the client • Collaborate with PM on monthly invoicing and variance management of clinical budget • Develop study related clinical documents • Identify and develop training needs for CRAs and third-party vendors • Generate potential site list from key stakeholders and drive site feasibility process • Identify potential risks to the enrollment targets based on feasibility analysis • Develop timely and effective communication and good working relationships with investigators and study team • Lead internal clinical team meetings and sets expectations for clinical team of CRAs and CTAs
• Bachelor’s degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred • Minimum of 5 years of clinical research experience or proven competencies for the position with significant clinical monitoring experience • Significant clinical monitoring experience in radiopharmaceuticals and/or radiolabeling • Ability to travel domestically and internationally including overnight stays • Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint) • Excellent communication and interpersonal skills to effectively interface with others in a team setting • Excellent organizational skills, attention to detail, and a customer service demeanor
• Discretionary annual bonus • Health insurance • Retirement savings benefits • Life insurance and disability benefits • Parental leave • Paid time off for sick leave and vacation
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