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Clinical research professional with comprehensive expertise in study design, data analysis, and regulatory compliance. Strong collaborator, adaptable to changing needs, and reliable in achieving project outcomes. Expertise in protocol development, patient recruitment, and quality assurance, combined with results-driven mindset. Valued for analytical skills, effective communication, and problem-solving abilities.

Experienced clinical trial project leader with a proven track record of over 20 years in successfully managing global programs consisting of multiple trials. Collaborates effectively with vendors, stakeholders, and multidisciplinary team members to ensure projects are completed within scope, on time, and within budget. Proficient in GCP/ICH and regulatory compliance, with strong abilities in budget forecasting, contract negotiation, and risk mitigation. Demonstrates expertise in building and overseeing departmental infrastructure, prioritizing budget allocation, resource management, and establishing standard operating procedures (SOPs), templates, and policies.

Experienced professional with an M.S. in Haematology and
Transfusion Medicine. I have over 9 years of relevant experience
in Medical Terminology and Coding (LOINC, SNOMED CT, ICD,
RxNorm, HGNC, and NCI)
Key Expertise:

  Clinical Terminology & Coding: LOINC, SNOMED CT, ICD, RxNorm, HGNC, NCI, VSAC, UMLS. Data Standardization: Lab, Medication, Diagnosis, Surgery, Tumor exam(Histology), Biomarker curation & harmonization for clinical research. AI & ML in Healthcare: NLP-driven model validation & clinical trial analytics. Digital Clinical Trials: Core I/E criteria analysis from sponsor protocols ( BMS, Abbive, etc). Big Data & Analytics: Large-scale clinical dataset processing &insights


Clinical Research Coordinator with 5 years of experience supporting all phases (Phase I-IV) of clinical trials across multiple therapeutic areas. Strong background in regulatory compliance, site operations, and monitoring support, with hands-on experience preparing sites for monitoring visits, maintaining audit-ready documentation, resolving data queries, and collaborating closely with CRAs, sponsors, and investigators. Motivated to grow into a CRC, CRA I, or In-House CRA roles.
Clinical Research Coordinator with experience in grants, Writing, drafting publications, designing study protocols, leading investigator meetings, and conducting clinical trials. Graduate student completing a Master of Science with an emphasis on neuroscience/neurosurgery research.

Bengi Acar

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Clinical Research Unit Manager

Site Coordinator

Brand Consultant

Molecular Biologist

Education

Molecular Biology and Genetics -

Bakırköy Anatolian High School -

English Language

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Clinical Research Unit Manager

Site Coordinator

Brand Consultant

Molecular Biologist

Molecular Biology and Genetics -

Bakırköy Anatolian High School -

English Language

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