Research Operations Coordinator
Research Operations Coordinator, Remote, Poland
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.
As a Project Specialist at ICON, you will support various project activities and contribute to the successful execution of clinical trials and projects within the healthcare and pharmaceutical industries.
What You Will Do:
You will take responsibility for scientific operations deliverables, applying your skills to ensure quality and efficiency.
Key responsibilities include:
Supporting project managers in the planning, execution, and monitoring of clinical trials.
Assisting in the development and maintenance of project timelines, budgets, and resource allocations.
Coordinating with cross-functional teams to ensure timely delivery of project milestones.
Managing study documentation and assisting in the preparation of regulatory submissions.
Contributing to the development and implementation of process improvements to enhance operational efficiency.
Your Profile:
You will bring relevant scientific operations experience, along with the following qualifications and skills.
Required qualifications and experience:
Bachelor's degree in life sciences, pharmacy, or a related field.
Previous experience in clinical research or project management preferred.
Strong organizational skills with the ability to prioritize tasks and meet deadlines.
Excellent attention to detail and accuracy in data management and documentation.
Effective communication skills, with the ability to work effectively across teams.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
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.
Are you a current ICON Employee? Please click here to apply
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.
As a Project Specialist at ICON, you will support various project activities and contribute to the successful execution of clinical trials and projects within the healthcare and pharmaceutical industries.
What You Will Do:
You will take responsibility for scientific operations deliverables, applying your skills to ensure quality and efficiency.
Key responsibilities include:
Supporting project managers in the planning, execution, and monitoring of clinical trials.
Assisting in the development and maintenance of project timelines, budgets, and resource allocations.
Coordinating with cross-functional teams to ensure timely delivery of project milestones.
Managing study documentation and assisting in the preparation of regulatory submissions.
Contributing to the development and implementation of process improvements to enhance operational efficiency.
Your Profile:
You will bring relevant scientific operations experience, along with the following qualifications and skills.
Required qualifications and experience:
Bachelor's degree in life sciences, pharmacy, or a related field.
Previous experience in clinical research or project management preferred.
Strong organizational skills with the ability to prioritize tasks and meet deadlines.
Excellent attention to detail and accuracy in data management and documentation.
Effective communication skills, with the ability to work effectively across teams.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
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.
Are you a current ICON Employee? Please click here to apply