GLOBAL FEASIBILITY & SITE ENGAGEMENT MANAGER

Global Feasibility & Site Engagement Manager

Advanced Clinical is a clinical development and strategic resourcing organization committed to providing a better clinical experience across the drug development journey.

Our goal is to improve the lives of all those touched by clinical research approaching each opportunity with foresight, character, resilience and innovation.

Based on decades of experience, we help our clients achieve better outcomes by conducting candid conversations and anticipating potential issues through our customized solutions.

The Global Feasibility & Site Engagement Manager is a member of the Global Feasibility and Site Engagement team responsible for conducting pre and post award protocol, country and site feasibility assessments.

This role leads and manages the process of end-to-end feasibility to support the business development and operational teams for assigned pre-award assessments and serves as the primary lead on post-award assessments with support from multi-functional subject matter experts.

This role directs all aspects of assigned feasibility assessments including developing feasibility questionnaires, researching / compiling site / KOL lists, driving cross-functional collaboration and feedback, compiling and assessing data analytics to produce meaningful recommendations, prepare feasibility findings report, presenting feasibility findings / recommendations to internal and external stakeholders, while meeting all time frames and targets to meet or exceed project milestones.

ESSENTIAL DUTIES AND RESPONSIBILITIES :

• Applies project management methodology, leadership and problem-solving skills to pre and post award feasibility assessments to support project level objectives, goals and deliverables.
• To perform as a technical expert in Feasibility process for internal and external clients and to provide strategic input to Business Development, Proposals, Operational Clinical Teams and Sponsors.
• Expertly mine, review, dissect and interpret clinical trial business intelligence information, data analytics, site reported data and systems in various formats to apply to individual assessments, drive multi-functional discussion and derive recommendations related to protocol, country, accrual rate and site components of assigned assessments.
• Facilitate discussions amongst cross functional areas, Executives, Sponsor team members, Key Opinion Leaders and site staff to obtain necessary information, goals, feedback and opinions related to assigned feasibility assessments.
• Review of study documents and preparation of summaries for teams involved in feasibility activities.
• Review of scientific literature and self-training pertinent to feasibility activities.
• Develop feasibility assessment questionnaires, input into survey tools, assess data and collate to develop meaningful metrics to drive recommendations and decisions.
• Author feasibility findings reports as primary deliverable and serve as primary presenter to Sponsor and other applicable audiences.
• Support, facilitate and engage with sites and PIs within and outside of site networks to encourage continued support, engagement and feedback for future assessments and potential study execution.
• Routine assessment of project financials and monthly review of invoices.
• Participate and / or manage other assigned activities to enhance the feasibility and site engagement offering, processes and overall Advanced Clinical mission.
• Ability to travel up to 10%

QUALIFICATIONS :

• BS or BA degree in life sciences, business or healthcare field or comparable experience.
• Minimum 5 years of professional experience in Clinical research and / or Drug Development, with at least 2 years in direct CRO Feasibility experience.

CRO experience should include working knowledge of conduct of protocol, country and site feasibility assessments, study management logistics, regulatory / start-up logistics, trial designs, and country-level nuances.

• Strong Pre-Award / Proposal Level Feasibility required ideally 3+ years of that experience required.
• In-depth knowledge regarding the drug development process, operational conduct processes and challenges within clinical
• Knowledgeable of frequently utilized feasibility systems in the CRO and trial conduct industry.
• Expertise in internal and external relationship
• Inquisitive in nature, enjoys researching to uncover what may not be readily available and detailed orientated.
• Must be able to see the big picture and project manage to the detail
• Excellent communication and presentation skills, including written, spoken and listening
• Demonstrated ability to work in a fast-paced
• Demonstrated ability to lead cross-functional teams, including those that are of higher seniority.
• Must have a positive demeanor with strong problem analytic and problem-solving skills.
• Must have exceptional time management skills and the ability to work with individuals across various levels of the organization, as well as individuals across all levels outside of the
• Consultative and collaborative approach when working with internal and external customers.
• Computer skills, including Excel, Word, PowerPoint and frequently utilized business intelligence tools (i.e. Citeline, Claims Databases, Impact Assessment Tools, Survey Tools, etc.)

At Advanced Clinical, our commitment to diversity and inclusion in every part of our organization is crucial to fulfilling our mission and demonstrating our REAL values.

A diverse staff allows us to effectively draw on different perspectives and enhance our efficiency and effectiveness. Diversity thereby strengthens the legitimacy and relevance of Advanced Clinical in delivering services to our clients.

We seek talented, creative individuals from a variety of backgrounds and cultures to work with us. It is our priority that our workplace be inclusive, welcoming of diverse ideas and appreciative of valuable experience.

Equal Employment Opportunity

It is Advanced Clinicals practice not to discriminate against any Employee or applicant because of sex, race, color, age, national origin, religion, gender, gender identity or expression, sexual orientation or sexual preference, pregnancy or maternity, genetic information, marital status, physical or mental disability, medical condition, military or veteran status, or any other basis protected by applicable federal, state, or local law.

This practice applies to all terms and conditions of employment including, but not limited to, hiring, training, compensation, benefits, promotions, transfers, layoff, Company-sponsored education, social and recreational programs, and treatment on the job.

If you have a disability or handicap and would like us to accommodate you in any reasonable way, please inform your Recruiter so that we can meet to discuss the appropriate alternatives available.