
Manager, Clinical Trial Management
Posted 8 hours ago

Posted 8 hours ago
This is a fully remote position, open to applicants in United States.
• Develop, mentor, coach, and oversee Clinical Trial Managers (CTMs) and Project Clinical Trial Managers (PCTMs) to enhance their skills in accordance with Precision for Medicine's quality standards. Promote individual growth and career advancement.
• Collaborate with the Clinical Operations Management Team and other functional management to continuously refine and improve CTM expectations and procedures, fostering quality, consistency, and efficiency in achieving established Key Performance Indicators (KPIs).
• Partner with the Resourcing team to ensure adequate allocation and fulfillment of Clinical Operations resources and requirements.
• Create action plans and offer strategic oversight to enhance CTM services, emphasizing high-quality delivery of individual, team, and departmental objectives.
• Provide continuous feedback and development to effectively manage the performance of direct reports.
• Offer technical support and guidance—including scope definition, risk identification, escalation and mitigation, resource planning, goals, and deliverables—to assigned CTMs.
• Ensure that all assigned CTMs have access to the necessary resources, training, materials, and systems to meet the expectations of their roles.
• Confirm that CTMs uphold high-quality standards and comply with established Standard Operating Procedures (SOPs), working guidelines, project plans, and all regulatory requirements.
• Ensure CTMs provide timely and precise updates of all required administrative documents (SOPs, T&E, etc.) on company systems.
• Exemplify and adhere to Precision’s values that focus on our commitment to quality, our people, clients, and performance.
• Undertake additional duties and departmental initiatives as directed by Leadership.
• A 4-year college degree or equivalent experience, preferably in a scientific or health-related discipline.
• A minimum of 5 years of industry experience in clinical research, including clinical operations experience within a pharmaceutical company or Clinical Research Organization (CRO), or demonstrated competencies relevant to this position.
• Proficiency in ICH GCP guidelines and the clinical development process.
• Exceptional communication and interpersonal abilities to effectively collaborate with others in a team environment.
• Strong organizational skills, attention to detail, and a customer service-oriented approach.
• Willingness to travel domestically and internationally, including overnight stays.
• Health insurance
• Retirement savings benefits
• Life insurance
• Disability benefits
• Parental leave
• Paid time off for sick leave and vacation
• Discretionary annual bonus
IQVIA
Precision Medicine Group
Natera
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