CTA

ICON Strategic Solutions; Sweden; On-site; SEK 40 000 - 80 000; Full time

Job summary

An established industry player is seeking a Clinical Trial Administrator to join their innovative team. This role involves coordinating clinical trials, maintaining documentation, and collaborating with cross-functional teams to ensure successful execution. The company fosters a creative and inclusive environment, offering a range of benefits including health insurance options and retirement planning schemes. Ideal candidates will have a background in scientific or healthcare fields and possess excellent organizational and communication skills. If you're passionate about clinical research and looking for a rewarding career, this opportunity is perfect for you.

Benefits

Health Insurance Options

Retirement Planning Schemes

Global Employee Assistance Programme

Life Assurance

Flexible Optional Benefits

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Prior experience or strong interest in clinical research.

Responsibilities

• Coordinate and administer clinical trials, ensuring adherence to protocols.
• Maintain and organize trial documentation including study files.

Skills

Organizational Skills

Communication Skills

Knowledge of Clinical Trial Processes

Collaboration

Education

Bachelor's Degree in Scientific or Healthcare-related Field

Job description

Job Title: Clinical Trial Administrator

We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team at ICON. In this role, you will assist with the design and analysis of clinical trials, interpret complex medical data, and contribute to the development of innovative treatments and therapies.

Location & Employment Details:

• Hours: Full Time
• Contract Type: Permanent
• Experience Level: Experienced (non-manager)

You will work closely with a single sponsor, fully embedded within their organization, partnering with a global pharmaceutical client known for its innovative product pipeline. This environment fosters creativity, collaboration, and high performance.

Responsibilities:

• Coordinate and administer clinical trials, ensuring adherence to protocols and regulatory standards.
• Maintain and organize trial documentation, including study files and regulatory submissions.
• Support the preparation of study materials such as informed consent and case report forms.
• Collaborate with cross-functional teams to facilitate communication and trial execution.
• Track and report clinical trial metrics and milestones.

Candidate Profile:

• Bachelor's degree in a scientific or healthcare-related field.
• Prior experience or strong interest in clinical research.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.
• Ability to work collaboratively in a fast-paced, detail-oriented environment.

What ICON Offers:

We value our people and are committed to a diverse, inclusive culture that rewards high performance and nurtures talent. Our benefits include:

• Various annual leave entitlements
• Health insurance options
• Retirement planning schemes
• Global Employee Assistance Programme
• Life assurance
• Flexible optional benefits such as childcare vouchers, gym memberships, and more

Learn more about working at ICON: https://careers.iconplc.com/benefits

ICON is dedicated to inclusion and equal opportunity. We welcome applications from all qualified candidates and provide accommodations for applicants with disabilities. For more information, visit https://careers.iconplc.com/reasonable-accommodations.

If you're interested but unsure if you meet all requirements, we encourage you to apply. You might be exactly what we're looking for!