Life Sciences Job at ICON | Study Start Up Associate | Apply Now
Getting a clinical trial off the ground is one of the most complex and critical phases of drug development. If you are eager to enter the industry and facilitate the initiation of these trials, this Study Start Up Associate I position is an exceptional Life Sciences Job. Available in Sofia, Budapest, Warsaw, and Gdansk (with remote or office-based flexibility), this role provides a structured entry point for a long-term ICON Career. For recent graduates or professionals looking to transition into a highly rewarding Clinical Research Job, this is where the journey of life-saving medicines begins.
About the Company
ICON plc is a world-leading healthcare intelligence and clinical research organization. They pride themselves on fostering an inclusive environment that drives innovation and excellence. When you embark on an ICON Career, you are joining a mission to shape the future of clinical development. Success here is built on a diverse culture that nurtures talent and rewards high performance. ICON supports its employees with comprehensive global and regional benefits, including competitive retirement planning, life assurance, flexible local perks (like childcare vouchers and gym memberships), and the Global Employee Assistance Programme, LifeWorks, which provides 24-hour access to well-being support.
Life Sciences Job – Key Responsibilities
The core of this Clinical Research Job involves delivering site start-up and activation work to an uncompromisingly high standard. As a Study Start Up Associate I, you will act as the crucial link between internal teams, external stakeholders, and regulatory bodies.
- Regulatory Submissions: Assisting in the preparation and submission of essential regulatory documents, such as clinical trial applications and ethics committee submissions.
- Stakeholder Coordination: Coordinating with various internal and external parties to obtain the necessary approvals and authorizations to successfully initiate the study.
- Documentation Support: Helping study teams develop core study documents, including protocols, informed consent forms, and investigator brochures.
- Record Maintenance: Ensuring that accurate and up-to-date records of all regulatory submissions and approvals are meticulously maintained to keep this Life Sciences Job fully compliant.
- Strategic Input: Participating actively in study start-up meetings and providing valuable input on regulatory requirements and timelines.
Candidate Profile For Life Sciences Job
ICON encourages applicants to apply even if they don’t meet every single bullet point—there is every chance your unique background is exactly what they need for this Clinical Research Job.
Required qualifications and experience:
- Education: A Bachelor’s degree in life sciences or a related field is required. This academic foundation is essential for succeeding in this Life Sciences Job.
- Experience Level: Previous experience in clinical research or regulatory affairs is preferred, but not required, making this an incredibly accessible entry point for highly organized professionals.
- Skillset: Strong attention to detail, exceptional organizational skills, and excellent communication abilities to collaborate effectively with cross-functional teams.
- Work Style: The ability to work independently and manage multiple tasks simultaneously in a fast-paced environment.
- Mobility: A willingness to travel occasionally as required (approximately 5%).
In summary, this Study Start Up Associate I role is an outstanding Life Sciences Job for those passionate about regulatory compliance and clinical trial activation. By securing this Clinical Research Job, you will directly contribute to the advancement of innovative treatments and therapies across Europe. Apply today to begin a fulfilling ICON Career and help shape the future of global healthcare.
