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Experienced Full Stack Pharmacoepidemiologist – Remote Research Associate for Walgreens Clinical Trials and Observational Studies

Worldwide Salaried Open

About Us

At Workwarp, we are a dynamic and innovative company that specializes in producing Real-World Evidence (RWE) through observational data to drive clinical research, inclusivity, and equity. We collaborate with industry leaders, including biopharmaceutical, biotechnology, clinical device, and digital healthcare organizations, to produce evidence that supports critical clinical and regulatory decision-making as well as market access growth. Our team is passionate about making a meaningful impact in the healthcare industry, and we are excited to invite a talented and motivated individual to join our team as a Full Stack Pharmacoepidemiologist.

About the Role

We are seeking an experienced Full Stack Pharmacoepidemiologist to join our team as a Remote Research Associate for Walgreens Clinical Trials and Observational Studies. As a key member of our team, you will be responsible for supporting the design, implementation, and analysis of observational studies, as well as collaborating with external partners to understand study objectives and project needs. This is an exciting opportunity to work with a dynamic team, develop your skills and expertise, and contribute to the production of high-quality RWE.

Key Responsibilities

As a Full Stack Pharmacoepidemiologist, you will be responsible for the following key responsibilities:
  • Collaborate with external partners to understand study objectives and project needs, and provide project management support for review and planned observational RWE studies.
  • Develop and implement statistical and analytical skills to support the design and lead of observational investigations, including data collection, analysis, and interpretation of results.
  • Support the development of research strategies and protocols applicable to the direct of RWE studies, and contribute to the translation and reporting of results.
  • Stay up-to-date with the latest trends driving the extended use of RWE, and collaborate with clients to develop and produce edited content, including articles, banners, and press releases.
  • Foster strong cross-functional relationships with other RWE and Clinical Trial groups, and contribute to the development of study protocols, including design and statistical considerations.

Essential Qualifications

To be successful in this role, you will need to possess the following essential qualifications:
  • Late graduate of a licensed program (epidemiology, biostatistics, bioinformatics) with a strong analytical component or other relevant unified health discipline.
  • Ability to support proposal development, including background research.
  • Ability to lead designated writing reviews.
  • Ability to support the development of study protocols, including design and statistical considerations.
  • Experience with electronic data management.
  • Direct data analysis and approval for observational studies.
  • Ability to combine results of observational studies in statistical reports, slide decks, and observational review reports.
  • Fundamental knowledge of healthcare/illness cycles and therapy.
  • Superb organizational and time-management skills.
  • Fastidious and ability to focus on and perform multiple tasks productively.
  • Proficient in Microsoft Excel, PowerPoint, and Word, as well as additional statistical packages.
  • Excellent oral and written communication skills combined with resilient relationship-building skills.
  • Ability to work across multi-disciplinary teams.
  • Able to travel up to/no less than 5% of the ideal time for business purposes (within state and out of state).

Preferred Qualifications

While not essential, the following preferred qualifications would be beneficial for this role:
  • Experience with clinical terminologies and controlled vocabularies used in healthcare data and ontologies (ICD9/10/Read Codes).
  • Experience with Good Pharmacoepidemiology Practice (GPP) or regulatory compliance rules for RWE studies.

Career Growth Opportunities and Learning Benefits

As a Full Stack Pharmacoepidemiologist at Workwarp, you will have the opportunity to develop your skills and expertise in a dynamic and innovative environment. You will work closely with a talented team of professionals who are passionate about making a meaningful impact in the healthcare industry. We offer a range of career growth opportunities, including:
  • Professional development and training programs to enhance your skills and expertise.
  • Opportunities to work on high-profile projects and contribute to the production of high-quality RWE.
  • Collaboration with industry leaders and experts in the field of pharmacoepidemiology.
  • Flexible work arrangements, including remote work options.

Work Environment and Company Culture

At Workwarp, we value a positive and inclusive work environment that supports the well-being and success of our employees. Our company culture is built on the following core values:
  • Collaboration and teamwork.
  • Continuous learning and professional development.
  • Innovation and creativity.
  • Customer focus and satisfaction.
  • Integrity and ethics.
We offer a range of benefits and perks to support the well-being and success of our employees, including:
  • Competitive salary and benefits package.
  • Flexible work arrangements, including remote work options.
  • Professional development and training programs.
  • Opportunities for career growth and advancement.
  • Recognition and rewards for outstanding performance.

How to Apply

If you are a motivated and talented individual who is passionate about making a meaningful impact in the healthcare industry, we encourage you to apply for this exciting opportunity. To apply, please click on the link below and submit your application. Apply To This Job We look forward to hearing from you and welcoming you to our team! Apply for this job

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