Job Description
The Clinical Safety Analytics Associate will play a critical role within the PV CoE. This position focuses on analyzing data and deriving insights from clinical and safety data sources to generate evidence and support decision-making across the organization. The Associate will leverage a variety of analytics and visualization techniques to contribute to clinical development, drug safety, and post-marketing activities.
ResponsibilitiesCollaborate and work closely with cross-functional teams including data analysts/engineers and business stakeholders to understand their needs and gather requirements.Clean, transform, and pre-process data to ensure data quality, consistency, and compatibility for analysis.Develop and implement data analysis plans to answer clinical and safety questions.Apply analytical and/or statistical techniques to analyze data and generate insights on safety questions.Visualize data and results to share insights with technical and non-technical cross-functional stakeholders.Interpret and communicate findings through reports, presentations, and visualizations.Stay up to date and compliant with the regulatory landscape related to drug safety and data analyses.Work closely with PV CoE and other stakeholders, sharing knowledge and best practices within the broader safety and analytics teams.Essential SkillsProficiency in programming languages such as SQL, Python, R, or SAS.4+ years of experience as a Data Analyst.Intermediate to Advanced skills with visualization tools such as Power BI or Qlik.Strong communication skills.Bachelor's or Master's (preferred) degree in a relevant field, such as Biostatistics, Analytics, Engineering or a related discipline.Additional Skills & QualificationsStrong understanding of data sources such as clinical trial data, electronic health records, and other healthcare databases.Proficiency in data pre-processing, cleaning, and transformation techniques.Knowledge of analytical and statistical methodologies such as regression analysis and survival analysis.Excellent problem-solving skills and the ability to derive meaningful insights from complex real-world data sets.Ability to work collaboratively in cross-functional teams and manage multiple projects simultaneously.Strong attention to detail and accuracy in data analysis and interpretation.Experience in the biopharma or healthcare industry is preferred.Work Environment
The candidate must be able to work 50% onsite in Lawrenceville. Local candidates are preferred. The candidate must be able to come in for an onsite in-person interview as a part of the process. This role is within a global biopharmaceutical company committed to sustainability and responsibility, creating a positive impact in the communities where we live and work.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our peopleThe company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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