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Job ID 2112448
Job Description
Join the forefront of healthcare innovation with ICON plc, a distinguished leader in healthcare intelligence and clinical research. At ICON, we cultivate an inclusive environment that inspires groundbreaking advancements and a commitment to excellence. Be a part of our mission to redefine the landscape of clinical development as we expand our dynamic team of Regional Clinical Scientists.
In this pivotal role, the Regional Clinical Scientist will collaborate closely with the Study Medical Monitor and Study Clinical Scientist to offer scientific and clinical expertise across a spectrum of early and late-stage clinical trials. Your primary focus will be on monitoring protocol-specific clinical data throughout the study. Serving as an essential liaison, you’ll engage with CROs, investigators, and study personnel to ensure daily safety monitoring under the guidance of the Medical Monitor. Reporting to Global Clinical Operations, you’ll interface directly with cross-functional teammates from Clinical Development, Data Management, Biometrics, Patient Safety, Clinical Pharmacology, and Biomarkers, all dedicated to executing clinical studies and efficiently monitor clinical data.
**Key Responsibilities**
- Assist the Study Clinical Scientist in medical surveillance and monitoring activities, conducting daily reviews of laboratory and ECG alerts, including eligibility criteria assessments.
- Analyze clinical trial data, addressing issues related to protocol conduct and subject safety effectively.
- Compile, review, and provide preliminary assessments of medical surveillance events, generating safety trackers, monitoring reports, and reviews based on study needs.
- Engage in cross-functional team efforts to ensure the successful execution of clinical data review activities.
- Contribute to informed consent forms (ICFs), training materials, and regulatory documentation under the guidance of the Medical Monitor/Study Clinical Scientist.
- Foster communication with internal and external stakeholders, supporting clinical trial objectives related to subject safety and data oversight; address and triage medical and safety-related inquiries as necessary.
- Perform additional tasks related to clinical programs as assigned.
**Qualifications**
- Degree in life sciences (BS, MS, or Ph.D.) coupled with clinical or pre-clinical research experience in the pharmaceutical or healthcare sectors.
- Proficiency in analyzing and interpreting clinical data, with a working understanding of GCP and clinical trial execution.
- Hands-on experience collaborating with clinical trial sites across various phases of drug development.
- Ability to make informed, timely decisions independently.
- Proven capability to manage multiple projects, demonstrating strong attention to detail, effective communication, and analytical skills.
- Capacity to thrive in a fast-paced, collaborative team environment while also functioning autonomously when needed.
- Exceptional organizational and project management capabilities.
- Adaptable to changing team and project demands.
What You Can Expect from ICON:
Our ongoing success is attributed to the exceptional quality of our team. We’re committed to fostering a diverse and rewarding culture that celebrates high performance and nurtures talent. Alongside a competitive salary, ICON provides a comprehensive benefits package tailored to your well-being and work-life balance. Examples of our benefits include:
- Diverse annual leave options
- A variety of health insurance plans to meet you and your family’s needs
- Competitive retirement planning programs to secure your future
- Global Employee Assistance Programme, TELUS Health, giving 24/7 access to a vast network of over 80,000 specialized professionals focused on your well-being
- Life assurance
- Flexible country-specific optional benefits, such as childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, and more.
Explore more about the benefits of building your career with ICON on our careers website. ICON is an equal opportunity employer, dedicated to creating a workplace free from discrimination and harassment. We welcome applications from all qualified individuals, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. Should you require accommodations during the application process due to a medical condition or disability, please let us know. Interested in this opportunity? Click apply for full job details.