Serves as the clinical trial lead responsible for the planning, conduct and oversight of the operational portion of clinical studies.
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 (e.g. clinical plans, Informed Consent Form templates, etc.).
Identify and develop training needs for CRAs and third-party vendors specific to the study.
Generate potential site list from key stakeholders and drive site feasibility process.
Identify potential risks to the enrollment targets based on feasibility analysis and site’s contracted commitment.
Develop timely and effective communication with investigators and study team.

Bachelor’s degree or equivalent combination of education/experience in science or health-related field.
Minimum of 7 years of clinical research experience or proven competencies for the position with significant clinical monitoring experience.
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.
Ability to travel domestically and internationally including overnight stays.

Clinical Trial Manager – Senior Clinical Trial Manager

Key skills