Karim Boudjemaa
42 Rue de la Liberté, Algiers 16000, Algeria
+213 21 345 6789 | karim.boudjemaa@email.com | linkedin.com/in/karimboudjemaa

PROFESSIONAL EXPERIENCE

Scientific Writer
Pharmatech Solutions, Boston, MA
June 2021 – Present

• Develop comprehensive regulatory documents including INDs, clinical study protocols, and investigator brochures for oncology and immunology drug development programs, ensuring compliance with FDA and EMA guidelines
• Author and edit scientific publications, conference abstracts, and presentation decks communicating preclinical and clinical pharmacology data to diverse audiences including regulatory agencies, healthcare professionals, and internal stakeholders
• Collaborate with cross-functional teams including clinical pharmacology, non-clinical pharmacology, and drug discovery departments to translate complex biochemistry and mRNA therapeutic data into clear, accurate scientific communications
• Manage competitive intelligence databases and prepare strategic briefing documents analyzing competitor oncology pipelines and emerging cancer therapeutic modalities
• Mentor junior writers on scientific writing best practices, document structure, and regulatory requirements, improving team efficiency by streamlining review processes
• Lead preparation of slide decks and brochures for licensing discussions and business development presentations, supporting evaluation of external drug development opportunities

Associate Scientific Writer
BioDynamics Inc., San Francisco, CA
August 2018 – May 2021

• Authored clinical and non-clinical sections of regulatory submissions for Phase I-III oncology trials, including pharmacology, toxicology, and clinical pharmacology modules
• Developed scientific content for investigator meetings, advisory boards, and medical conferences, translating in vitro and in vivo study results into compelling narratives
• Conducted literature reviews and maintained reference databases to support evidence-based medical writing for drug development programs
• Prepared validation documents and standard operating procedures for scientific communication processes
• Supported business development scouting activities by creating competitive intelligence reports on emerging cancer therapeutics and novel drug delivery platforms

Research Associate
Genomic Research Labs, Cambridge, MA
January 2016 – July 2018

• Conducted in vitro and in vivo pharmacology studies investigating novel oncology compounds, utilizing fluorescence microscopy and biochemical assays
• Analyzed experimental data and authored technical reports, study protocols, and internal communications documenting research findings
• Presented research results at departmental meetings and contributed to scientific publications in peer-reviewed journals
• Collaborated with medicinal chemistry teams to optimize lead compounds and support drug discovery programs
• Maintained detailed laboratory records and managed research databases ensuring data integrity and regulatory compliance

EDUCATION

Master of Science in Pharmacology
University of Lyon, Lyon, France
Graduated: May 2015

Bachelor of Science in Biochemistry
University of Algiers, Algiers, Algeria
Graduated: May 2013

SKILLS

Scientific Writing & Communication: Regulatory writing (IND submissions, protocols, investigator brochures), medical writing, publications, scientific presentations, presentation skills, written communication

Drug Development: Clinical pharmacology, non-clinical pharmacology, oncology, drug discovery, cancer therapeutics, mRNA therapeutics

Scientific Expertise: Biochemistry, chemistry, pharmacology, in vitro/in vivo methodologies, fluorescence microscopy

Business & Strategy: Competitive intelligence, licensing support, scouting, business development communications

Technical Tools: Microsoft Office Suite, Microsoft Project, scientific databases, reference management systems

Languages: English (native), French (professional proficiency), Arabic (native)

Professional Attributes: Detail-oriented, strong planning and organizational skills, mentoring capabilities

ADDITIONAL INFORMATION

• Active participant in medical writing and regulatory affairs professional organizations
• Regular attendee at oncology and drug development conferences
• Experienced in preparing materials for advisory boards and investigator meetings