project manager for clinical trials

Enfint; Warszawa; On-site; PLN 120,000 - 180,000; Full time

Benefits offered by this job

Health insurance

Annual leave

Retirement plan

EAP access

Life assurance

Country-specific benefits

Job summary

ICON plc is a world-leading healthcare intelligence and clinical research organization. We support the development of innovative treatments and therapies through clinical research and trial management.

We are seeking a capable Clinical Project/Program Manager to oversee workstreams, assist PMs, coordinate sites and patient recruitment, and contribute to protocols and regulatory submissions in a fast-paced, team-oriented environment with travel up to 10%.

Qualifications

• Bachelor’s degree in a relevant scientific discipline or healthcare-related field.
• At least 2 years of experience in clinical research or project management.
• Strong organizational and multitasking skills.
• Excellent communication and interpersonal skills.
• Ability to work effectively in a fast-paced and team-oriented environment.
• Willingness to travel as required, approximately 10%.

Responsibilities

• Oversee project and programme management workstreams, ensuring deliverables meet quality and timeline expectations.
• Assist project managers with the planning, execution, and monitoring of clinical trials.
• Coordinate study activities, including site selection, patient recruitment, and data collection.
• Support the development of study protocols, case report forms, and other study-related documents.
• Participate in data analysis and interpretation to support decision-making and regulatory submissions.
• Collaborate with cross-functional teams to ensure project milestones are met and deliverables are achieved.

Skills

Project coordination

Organization

Communication

Team collaboration

Travel readiness

Education

Bachelor’s degree in a scientific/healthcare field

Job description

Описание

ICON plc is a world-leading healthcare intelligence and clinical research organization. It supports the development of innovative treatments and therapies through clinical research and trial management.

Задачи

• Oversee project and programme management workstreams, ensuring deliverables meet quality and timeline expectations.
• Assist project managers with the planning, execution, and monitoring of clinical trials.
• Coordinate study activities, including site selection, patient recruitment, and data collection.
• Support the development of study protocols, case report forms, and other study-related documents.
• Participate in data analysis and interpretation to support decision-making and regulatory submissions.
• Collaborate with cross-functional teams to ensure project milestones are met and deliverables are achieved.

Требования

• Bachelor’s degree in a relevant scientific discipline or healthcare-related field.
• At least 2 years of experience in clinical research or project management.
• Strong organizational and multitasking skills.
• Excellent communication and interpersonal skills.
• Ability to work effectively in a fast-paced and team-oriented environment.
• Willingness to travel as required, approximately 10%.

Условия

• Competitive salary
• Various annual leave entitlements
• Health insurance offerings for employees and their families
• Competitive retirement planning offerings
• Global Employee Assistance Programme with 24-hour access to a global network of specialized professionals
• Life assurance
• Flexible country-specific benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, and health assessments.