IVD Clinical Study Manager (Pathology Labs)

Meaningful work paired with a world class team.

ICON plc has a hot opening for an IVD Clinical Study Manager with pathology lab experience. In the role of a CTM or Study Manager, you will be the relationship partner at the clinical site level. The Pathology Study Manager will be working with the appropriate teams for the ICF creation and systems validations. As a CTM, you will work with the clinical trial team and review the performance of the trial, assess if the instruments are working currently at the site level, develop training & facilitate site training plans. You will also work closely with the testing sites.

Responsibilities:

• Leads the global study team with full accountability for the study with respect to quality, cost and timelines.
• Develops study design for technical studies in coordination with internal/external experts and the development project team
• Provides input to study synopsis prepared by CST for Clinical Utility and Clinical Performance studies and ensures that these Studies are planned and executed based on study synopsis with full responsibility for study protocol and study report
• Ensures that all studies are planned, executed, monitored, closed out and documented in a competent and compliant way within the planned time frame and costs.
• Ensures that the study results are continuously validated, assessed, clear recommendations drawn and communicated.
• Oversight of data management processes, data quality and results, data base closure and reporting.
• Ensures that data and reports which are necessary for the characterization, regulatory approval and marketing of the products have been agreed upon, made available and are documented in a timely fashion.
• Ensures and is responsible that study results are presented or submitted for publication in alignment with publication plans
• Planning of the study specific content and budget within the development project team and controlling the related agreed upon budgets during the study.
• Managing study site and clinical study agreements
• Delegation and oversight of tasks and work packages for internal and external collaborators within the study.
• Planning, procurement, preparation and delivery of materials necessary for carrying out the study, in cooperation with the Study Support team.
• Ensure compliance to all relevant safety and QM procedures in all studies.

Qualifications:

• Minimum - Bachelor's degree in medical technology, chemistry, biology or other science relevant field
• Four (4) or more years of Clinical Trial Manager/Study Manager experience in a CRO/Pharma/Biotech company required
• Knowledge of applicable standards and regulations for clinical trial and lab conduct
• Proven related experience in pathology
• Experience in all stages of international clinical study management, study protocol design, report writing and monitoring and leading local teams
• Proven planning, organizing, interpersonal and leadership skills
• Ability to work independently to make sound decisions and analyze and solve problems
• Demonstrated experience in computer skills to include Microsoft Word, Excel and basic templates
• Statistical knowledge

Benefits of Working in ICON:

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.