Open to opportunities

Chloe Citalois

@chloecitalois

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Passionate clinical research professional with expertise in trial management.

United Kingdom

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What I'm looking for

I am looking for a role that offers opportunities for growth, collaboration, and impactful contributions to clinical research.

I am a passionate and highly motivated clinical research professional with hands-on experience in clinical operations, regulatory affairs, and trial site coordination across global studies. My background in biochemistry and drug discovery, combined with my ability to lead and mentor cross-functional teams, positions me well for a transition into a Clinical Trial Manager role.

I bring in-depth knowledge of ICH-GCP, EU-CTR processes, site start-up, and trial monitoring fundamentals. My recent role as a Senior Clinical Operations Specialist at Syneos Health has allowed me to support site feasibility, selection, and initiation across global studies, ensuring compliance and guiding project delivery as a Subject Matter Expert for WEMEA.

As a finalist for the 2025 International Clinical Researcher awards, I have demonstrated my commitment to excellence in the field. I am eager to leverage my skills in clinical trial operations and regulatory compliance to contribute to impactful research initiatives.

Experience

Work history, roles, and key accomplishments

Current

Senior Clinical Operations Specialist

Current

Syneos Health

Jan 2024 - Present (1 year 6 months)

Supported global study feasibility, selection, and initiation, managing tasks across all phases (1-3) from start-up to closeout. Reviewed regulatory documentation, acted as a Subject Matter Expert for WEMEA, and mentored junior staff, including site monitoring and vendor oversight.

Regulatory Compliance ICH GCP EU CTR CTMS Risk Mitigation Mentoring

Clinical Operations Specialist

Syneos Health

Feb 2022 - Present (3 years 5 months)

Assisted with daily clinical trial activities, including eTMF tracking and direct liaison with research sites for submissions and training. Participated in clinical trial monitoring activities under supervision, acting as a Subject Matter Expert.

ETMF Site Submissions Regulatory Compliance

Regulatory Executive

Roche

Sep 2021 - Present (3 years 10 months)

Supported regulatory submissions and global labelling activities, ensuring compliance with product lifecycle management. Coordinated SmPC and label updates to align with evolving regulations.

Regulatory Submissions Product Lifecycle Management Regulatory Compliance

Pharmaceutical Consultant Intern

Pharma Targeting

May 2021 - Present (4 years 2 months)

Conducted comprehensive research for client portfolios, focusing on regulatory pathways and market analysis. Provided strategic advice on drug development and licensing opportunities.

Market Research Regulatory Pathways Licensing Client Management

Lab Assistant

Queen Mary University

Sep 2019 - Present (5 years 10 months)

Gained practical research experience in a university laboratory setting, including PCR testing and various lab protocols. Developed and implemented experimental procedures.

Lab Protocol Development Research Biochemistry Data Collection

Education

Degrees, certifications, and relevant coursework

University College London

MSc, Drug Discovery and Pharma Management

Grade: Distinction

Completed a Master of Science degree with Distinction, focusing on the principles of drug discovery and pharmaceutical management. Gained in-depth knowledge of the drug development lifecycle and industry regulations.

Queen Mary University of London

BSc, Biochemistry

Grade: 2:1

Undertook a Bachelor of Science degree in Biochemistry, achieving a 2:1 classification. Developed a strong foundation in biochemical principles and laboratory techniques.