Regulatory Affairs Associate – CTA, Fixed Term Contract

This is a fully remote position, open to applicants in Poland.

📋 Description

• Assist in the compilation of core package builds, contributing to Clinical Trial Applications and drafting necessary documentation.

• Identify, report, and address issues that could affect submission builds or the logistics of global submission delivery to regional and local partners or Health Authorities.

• Ensure that the project team is well-informed about the contract scope.

• Discover new business opportunities arising from changes in scope.

• Maintain client satisfaction through the delivery of professional services.

• Provide consulting services within your area of expertise under the supervision of a Project Lead or Technical Subject Matter Expert (SME).

• Produce high-quality work that meets the expectations of the project lead and client.

⛳️ Requirements

• A minimum of a Bachelor’s Degree in a Scientific or Technical Discipline.

• Initial years of experience in a CRO/Pharma setting.

• Background in Regulatory Affairs.

• A client-focused approach to work.

• Exceptional interpersonal and intercultural communication skills, both written and verbal.

• Strong critical thinking and problem-solving abilities.

• Proficiency in English and the local language, both written and spoken.

🏝️ Benefits

• Temporary contract duration of 17 months.

• Training and insight into the organization’s foundational consulting models and methodologies.

• Basic understanding of the services offered by Parexel.

• Assistance from senior staff on more complex tasks.

• Possible eligibility for Parexel’s annual performance-based bonus plan.

• Annual salary review.

• Total rewards incentives for qualifying roles.