Clinical Trial Feasibility Analyst
Science 37
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See open jobs at Science 37.See open jobs similar to "Clinical Trial Feasibility Analyst" Lux Capital.This role will be onsite in our Morrisville, NC office.
POSITION OVERVIEW
Science 37’s mission is to accelerate clinical research by enabling universal trial access for patients. Through our solutions; The Metasite™ and Patient Recruitment, we accelerate enrollment by expanding the reach of clinical trials to patients beyond the traditional site and rigorously qualifying patients prior to referring them to a traditional site. Our solutions are powered by a proprietary technology stack with in-house medical and operational experts that enhance quality through standardized workflows and best-in-class study orchestration.
We are looking for a dedicated and analytical Clinical Trial Patient Recruitment Feasibility Specialist to join our dynamic team. This role is pivotal in optimizing our patient recruitment efforts for clinical trials by utilizing advanced analytical techniques and data-driven insights. The ideal candidate will possess a strong understanding of clinical trial processes and will work closely with various stakeholders to ensure recruitment goals are met efficiently and effectively.
DUTIES AND RESPONSIBILITIES
Duties include but are not limited to:
- Analytical Focus: Conduct comprehensive data analysis to identify trends, opportunities, and challenges in patient recruitment.
- Heatmap Development: Create detailed heatmaps to visually represent areas with high recruitment potential, helping to target recruitment efforts more precisely.
- Proposal Support: Collaborate with the proposals team to provide robust data and insights that enhance the feasibility and success of patient recruitment strategies.
- Funnel Building: Design and implement recruitment funnels to monitor and optimize the patient recruitment pipeline.
- Recruitment Curves: Develop and analyze recruitment curves to forecast and track recruitment progress, ensuring alignment with project timelines.
- Diversity Mapping: Generate and maintain diversity maps to promote inclusive recruitment practices and ensure a diverse patient population.
- Stakeholder Collaboration: Work with cross-functional teams, including clinical operations, data management, and marketing, to align recruitment strategies with overall project goals.
- Reporting: Prepare and present detailed reports on recruitment metrics, progress, and projections to senior management and other stakeholders.
QUALIFICATIONS & SKILLS
Qualifications
The following qualifications are preferred and/or equivalent applicable experience:
- Bachelor’s degree in a relevant field (e.g., Life Sciences, Data Analytics, Statistics, or a related discipline).
- Proven experience in patient recruitment for clinical trials, with a strong analytical background.
- Proficiency in data analysis and visualization tools (e.g., Excel, Tableau, R, SAS).
- Excellent problem-solving skills and attention to detail.
- Strong communication and presentation skills, with the ability to translate complex data into actionable insights.
- Ability to work collaboratively in a fast-paced, team-oriented environment.
- Knowledge of regulatory requirements and ethical considerations in clinical trials is a plus.
Preferred Qualifications
- Master’s degree or higher in a related field.
- Experience with advanced statistical analysis and predictive modeling.
- Familiarity with clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
Skills/Competencies
- Strong communication and presentation skills – Excellent interpersonal skills and professional demeanor. Must have the ability to communicate accurately and clearly, both orally and in writing.
- Computer skills - Working knowledge of MS Office suite and Google applications. Able to generate business correspondence, create forms and generate reports as required. Proficiency with MS PowerPoint required.
- Knowledge of field organizational strategies - The ability to adapt to a rapidly changing work environment. Successful decentralized team management and situational responsive decision-making.
- Extensive knowledge of clinical research - Understands the drug development process. Knowledgeable about the critical elements for success in clinical trials; participation in and contribution to these activities.
- Team management and collaborative capabilities – Commitment to collaboration, within and across departments. Leverages each team member’s unique background and perspective to achieve team goals while providing clear direction and accountabilities.
- Interpersonal Savvy - Understands interpersonal and group dynamics and reacts in an effective and tactful manner. Has a range of interpersonal skills and approaches with ability to select a best-fit approach.
- Practices professionalism and integrity in all actions – Demonstrated ability to foster concepts of teamwork, cooperation, self- control, and flexibility to get the work done. The ability to adapt to a rapidly changing work environment. Able to successfully work in a decentralized team environment. Skilled in situational responsive decision-making.
- Excellent problem-solving and people skills- Communicate ideas effectively to resolve conflicts and achieve business goals.
- Practices professionalism and integrity in all actions – Demonstrated ability to foster concepts of teamwork, cooperation, self- control, and flexibility to get the work done.
- Ability to work independently, self-directed, strong work ethic and adherence to deadlines.
- Ability to be flexible and capable of working independently or as part of a team.
Capabilities
- Up to 10% travel, as needed, for project team meetings, client presentations and other professional meetings/conferences as needed
- Ability to communicate in English (both verbal and written)
REPORTING
Position reports to the Sr. Director, Channel Marketing & Global Healthcare Partnerships. The reporting leader will assign projects, provide general direction and guidance. Incumbent is expected to perform duties and responsibilities with minimal supervision.
Science 37 is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.
Science 37 values the well-being of its employees and aims to provide team members with everything they need to succeed.
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This job is no longer accepting applications
See open jobs at Science 37.See open jobs similar to "Clinical Trial Feasibility Analyst" Lux Capital.