We are Growing! Let us support your career journey the Biorasi way. Innovative, Collaborative, Dynamic and Evolving. Capitalizing on your strengths while encouraging work-life balance. Biorasi is an award-winning, customer-focused, full-service clinical research organization.

Biorasi is looking for top performers who are as passionate about clinical research as we are – clinical trial veterans and industry newcomers who will thrive in our fast-paced environment and help us drive new therapies to patients. Here is your chance to become a vital part of a growing global company in the expanding clinical research industry.

Your role:

Prepare and coordinate preparation of submission specific documents for initial submissions und amendments
Work independently on Ukrainian Regulatory submissions activities
May coordinate translation of submission specific documents
Coordination and execution of submissions and query responses to Regulatory Authorities and Ethics Committees / IRBs in the assigned regions, including safety related submissions
Provide regulatory advice to project teams and key internal/external stakeholders for start-up and maintenance activities in the assigned clinical projects
Ensure high quality of all regulatory documents
Track all submissions and responses to / from competent authorities and Ethic Committees / IRBs in a timely manner
Participate in internal and external teleconferences and project team meetings
Assess regulatory intelligence to assist in the development of local, regional, and global regulatory strategies
Participates in advocacy activities of a technical and/or tactical nature
Provides training on national / regional legislation, country requirements to other project team members
Prepares in cooperation with the PM the study specific regulatory plan
Support the QA department to prepare for and during Audits and Inspections regarding regulatory related aspects
Supports writing SOPs for the Regulatory Affairs department
Support Legal/Contracting team to address regulatory issues

Your Profile:

Bachelor’s Degree in biomedical sciences or related scientific discipline.
Fluent English (oral and written) and local language.
5-8 years in drug development and/or regulatory affairs within the pharmaceutical or related industry.
Experience in clinical trial process
Solid expertise in clinical trial regulatory submissions in Ukraine
Knowledge of guidance documents, regulatory legislation, various international regulatory requirements, and approval procedures in the assigned countries. Working knowledge of ICH/GCP principles.

If you have the experience required and want to join an energetic, creative, and collaborative team, please apply directly to our website at https://biorasi.com or email us at [email protected].

Biorasi is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. Biorasi is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

Specialist, Regulatory Affairs Contractor

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