Clinical Site Management Lead I (Nationwide)

Astellas Pharma • Northbrook, IL

2d • Remote

About The Position

Astellas is a global life sciences company committed to turning innovative
science into VALUE for patients. We provide transformative therapies in disease
areas that include oncology, ophthalmology, urology, immunology and women's
health. Through our research and development programs, we are pioneering new
healthcare solutions for diseases with high unmet medical need. Learn more at
Astellas.com.

Are you driven to make a real difference in the lives of patients?

We're seeking passionate individuals who thrive in dynamic environments, embrace
new ideas, and aren't afraid to take intelligent risks. People who act with
unwavering integrity and are deeply committed to making a tangible impact.

Purpose & Scope

This position is accountable for the direct management of assigned
monitoring/site management related clinical trial staff across all clinical
trial types, which may include pre/post-POC interventional drug trials, Clinical
Pharmacology normal healthy volunteer clinical trials, pre-approval access and
post-marketing regulatory commitment trials (interventional and
non-interventional).

Accountable for the identification, onboarding, training and development of
monitoring clinical trial talent to support the planning, initiation, execution
and close-out of clinical trials with operational excellence. Individuals in
this role will also provide leadership/mentorship, in a matrix setting, for
activities that support clinical trial teams.

This position is accountable to the Head, Early or Late Stage Site Monitoring &
Management, and will provide input into departmental budget and resourcing
strategies, including development and implementation of global processes and
procedures, non-drug product initiatives, and coaching of monitoring staff
during execution of development trials.

Requirements

• BA/BS degree with at least 8 years of executing global drug development programs and trials
• Minimum of 4 years site monitoring and direct people management experience
• Demonstrated leadership skills and ability to effectively collaborate with colleagues in Clinical Operations and cross-functionally to deliver on portfolio deliverables and objectives
• Must have extensive expertise in risk based monitoring strategies and strong knowledge of ICH/ GCP guidelines and multinational clinical trial regulations
• Must have experience working across multiple phases of development and in multiple therapeutic areas
• Demonstrated ability to successfully identify and lead global process or system improvement initiatives
• Must have a strong knowledge of clinical development processes and conducting global clinical programs
• Must have proven leadership skills and effective written and verbal communication skills
• Fluent in English. Depending on hiring region, may also be required to be fluent in local language.
• Moderate (~30%) travel required

Nice To Haves

• Advanced Degree

Responsibilities

• Responsible for resource planning, recruitment, mentoring, development and retention of site monitoring & management staff
• Manages and allocates monitoring resources to trials and monitor performance on assigned trials for monitoring staff (up to 12 direct reports)
• Provides direction, leadership and learning opportunities to enhance individual development of direct reports in support of providing best-in-class site monitoring across the portfolio
• Provides oversight and guidance in completing monitoring and site management related activities according to agreed timelines and quality standards, including identifying areas for additional training and development
• Oversees adherence to timelines, standards, processes for work assigned to their staff
• Serves as a point of escalation for clinical monitoring/site management related topics or issues from their staff
• Oversees and provide guidance to Clinical Operations Leads and/or Clinical Trial Leads in regional Key Opinion Leader (KOL) interactions, communications; and submissions to Health Authorities within their region/country of responsibility, aligned to the overall asset strategy.
• Responsible for compliance of direct reports with training and identification and support for any training needs
• Facilitates and supports global trial monitoring operational standards and tools
• Anticipates, recognizes and facilitates problem solving to support site monitoring & management staff and rapidly addresses and mitigates potential performance issues
• Collaborates effectively with portfolio operations Leads, clinical operations leads, Center of Excellence and PECs leadership to ensure site monitoring & management staff are delivering as expected and to ensure common framework and standards across clinical programs and trials
• Ability to collaborate with peers in Clinical Operations across Early and Late-Stage Clinical Operations, cross-functionally and regionally, including relevant counterparts globally, to align on best practices for clinical monitoring staff
• Identifies, escalates, and facilitates process improvements relevant to clinical trial monitoring and site management
• Contributes to development and implementation of best in class monitoring/site management standards and processes

Benefits

• Medical, Dental and Vision Insurance
• Generous Paid Time Off options, including Vacation and Sick time, plus national holidays including year-end shut down
• 401(k) match and annual company contribution
• Company paid life insurance
• Annual Corporate Bonus and Quarterly Sales Incentive for eligible positions
• Long Term Incentive Plan for eligible positions
• Company fleet vehicle for eligible positions
• Referral bonus program

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees