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Pharmaceutical Research Specialist

2 months ago


London, Greater London, United Kingdom Lifelancer Ltd Full time

Job Title: Research Assistant in Data Analysis

About the Role:

Lifelancer Ltd is seeking a highly skilled and experienced Freelance Pharmaceutical Research Specialist to join our team. As a key member of our research team, you will be responsible for conducting in-depth research and analysis in the pharmaceutical field.

Key Responsibilities:

  • Clinical Research: Conduct comprehensive research on clinical trials, drug efficacy, safety profiles, and patient outcomes. Utilize various research methodologies to gather and analyze data from clinical studies and medical literature.
  • Regulatory Compliance: Stay updated on regulatory requirements and guidelines from agencies such as the FDA, EMA, and other global health authorities. Ensure research and documentation adhere to these regulations.
  • Data Analysis: Analyze complex datasets from clinical trials and pharmaceutical studies. Use statistical tools and software to interpret data and derive meaningful insights.
  • Literature Review: Perform systematic reviews of scientific literature to gather information on new drugs, therapeutic approaches, and industry advancements.
  • Competitive Intelligence: Provide insights and recommendations based on competitive analysis.
  • Scientific Writing: Prepare scientific manuscripts, research reports, white papers, and regulatory submissions. Ensure accuracy, clarity, and compliance with scientific standards.
  • Collaboration: Work closely with cross-functional teams, including RD, regulatory affairs, clinical operations, and marketing, to align research findings with business objectives.
  • Innovation: Identify opportunities for innovation in pharmaceutical research and development.

Qualifications:

  • Experience: Minimum of 1 year in pharmaceutical research, clinical research, medical writing, or related fields.
  • Research Skills: Proficiency in research methodologies, data analysis, and scientific literature review. Experience with clinical trial protocols and regulatory documentation.
Regulatory Knowledge: In-depth understanding of regulatory requirements and guidelines for pharmaceutical research.Detail-Oriented: High attention to detail and accuracy in research and documentation.