Perform data analysis and present experimental data clearly and concisely to the project manager and supervisors at any time, including weekly laboratory meetings, Constructing and evaluating attenuated bacterial vaccines to prevent infections in humans and agriculturally important animals, Conducting immune response analyses and challenge studies as parts of the evaluations, Performing aseptic microbiological techniques, Preparation and purification of DNA, RNA, and proteins, Performing genetic manipulation and modification of pathogenic bacteria, Working with research animals, primarily mice, Synthesizing information from a variety of sources and ability to interpret results, Culturing bacterial isolates to evaluate their role in preventing infections in humans and experimental animals, Conducting challenge studies as parts of the evaluations, Preparation and purification of DNA, RNA and proteins, Performing genetic manipulation and modification of bacteria, Strong medical and scientific writing skills and the clear ability to understand, interpret and communicate scientific data, Medical affairs experience or clinical development experience with deep understanding of medical affairs, Knowledge of medical affairs or experience of developing claims substantiation routes from literature or by developing clinical testing, Experience in interpreting Real World and clinical data for purposes of formulary decision making or clinical insights would be advantageous, Experience of researching and scanning various internal and external databases and scientific literature, Experience working within an Alliance is helpful but not essential, Proven experience in the pharmaceutical and/or consumer goods industry, Excellent presentation skills in front of diverse and large audiences, Intermediate skills in application of statistical and epidemiological methods to pharmacovigilance, Literature Surveillance: source document review knowledge and skills, Leadership skills to potentially lead others in larger projects, Previous management and or mentoring experience, Excellent attention to detail, technical editing and QC skills, Strong experience in a biotech/pharmaceutical setting, Experience working with Hollow Fiber Bioreactors, Experience working with Mycobacterium tuberculosis, A good understanding of more than one development function, Other skills-intermediate skills in the following, Strong Written and verbal communications skills, including medical/scientific writing, Organization, prioritization, planning skills, Meeting management and time management skills, Pharmacovigilance skills-intermediate knowledge of the following, Presentation skills for conveying complex technical contents to non-expert audiences, Biomedical Literature-intermediate skills, Experience in leading teams and or projects, Significant clinical drug development or medical affairs experience within a pharmaceutical company environment, Influencing and negotiation in a cross-functional, matrix environment, Inter-relationship across various pharmacovigilance processes and documents, including reference safety information and product labeling, Advanced understanding of interfaces across various pharmacovigilance and risk management processes, Document writing and source document review, Critical scientific assessment and problem solving, Work collaboratively in a cross functional setting, Intercontinental Region (IC) is represented by 3 sub-geographies: Canada, Latin-America and TMEA (Turkey, Middle East and Africa), Serve as a medical resource to Gilead’s HIV Therapeutic Sales Specialists, Exhibit Gilead’s core values: integrity, teamwork, accountability, and excellence, Implement defined goals and objectives aligned with Medical Affairs’ strategic initiatives; develop plan for cultivating, and maintaining working relationships with existing and future thought leaders in assigned geographic territory, Maintains working knowledge of the treatment landscape, including competitors’ plans with ability to integrate into the overall Medical plan for the product/disease, Interpret clinical trial data and participate in safety assessments, Review scientific literature and provide support to the global scientific communications team, Strong intellectual curiosity with an appetite for exploring new and previously uncharted territories with an openness to change and ability to think outside the box, Work closely with the medical and clinical leadership team to ensure standards of medical & clinical governance are implemented across the organisation, Maintain working knowledge of the treatment landscape, including competitors’ plans, generating and analyzing valuable insights and translating them into action. • Direct involvement with P30 grant submission SRG is working with a global biopharmaceutical company who range of products include medicines, vaccines, consumer healthcare products and medical devices (injectables). Resume SamplesThis page provides you with Senior Research Scientist resume samples to use to create your own resume with our easy-to-use resume builder. Presentation is important. Develop and execute analytical test methods and controls for the manufacture of cell-based biological products. More than 1000 Free Sample Resumes ... maintained, calibrated, cleaned, and tested sterility of medical laboratory equipment.