At a Glance
- Tasks: Design and manage clinical trials, analyse data, and solve challenges in healthcare.
- Company: Join ICON, a global leader in healthcare intelligence and clinical research.
- Benefits: Competitive salary, health coverage, retirement plans, and career development opportunities.
- Other info: Inclusive workplace with a focus on collaboration and professional growth.
- Why this job: Make a real impact on patient care by advancing innovative treatments.
- Qualifications: Bachelor's degree and 5 years of experience in clinical trial management.
The predicted salary is between 42750 - 52250 £ per year.
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients, and suppliers.
We are currently seeking a Global Study Manager to join our diverse and dynamic team. As a Global Study Manager at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
What you will be doing:
- Collaborate with cross-functional teams to design and implement effective clinical trial enrollment.
- Oversee and manage the day-to-day operations of clinical trials, ensuring compliance with regulatory standards.
- Analyze and interpret clinical trial data, identifying trends, and providing insights to optimize study outcomes.
- Proactively address challenges and implement effective solutions to ensure the successful execution of clinical trials.
- Communicate effectively with internal and external stakeholders to foster strong partnerships and facilitate smooth trial processes.
Your profile:
- Bachelor's degree in a relevant field, with a minimum of 5 years of experience in global clinical trial management.
- Proven expertise in designing and executing clinical trials, with a strong understanding of regulatory requirements.
- Exceptional analytical and problem-solving skills, with the ability to interpret complex medical data.
- Effective communication and interpersonal skills, with the ability to collaborate across diverse teams.
- Detail-oriented and organized, with a track record of successfully managing multiple tasks and priorities simultaneously.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits:
- Competitive base salary and performance-related incentives.
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
- Retirement and pension plans.
- Life assurance and disability coverage.
- Employee assistance programmes and wellbeing resources.
- Learning and development opportunities through structured training and career pathways.
Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility:
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Summary Location: Poland, Warsaw; Romania, Bucharest; Hungary, Budapest; Bulgaria, Sofia; Regional Great Britain (Northern Ireland) Type: Full time
Travel Manager (Contract) employer: Icon Clinical PLC
At ICON, we pride ourselves on being a values-driven organisation that fosters a collaborative and inclusive work culture. As an Operation Program Specialist, you will not only contribute to meaningful healthcare projects but also benefit from our comprehensive rewards package, including competitive salaries, health programmes, and robust career development opportunities. Join us in Sofia, Warsaw, or Swansea, where your expertise will be valued and your professional growth supported in a dynamic environment dedicated to bringing new treatments to patients faster.
