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Clinical Study Analyst, Remote US

Company: TriNetX
Location: Irvine
Posted on: January 15, 2022

Job Description:

This position reports to our global HQ in Cambridge, MA, and is remote within the US. Travel is expected when needed and local candidates or East Coast based candidates are highly preferred.

Who we are:---

TriNetX---was founded on the idea that incorporating real-world data results in better clinical trial design, improves the site selection and patient recruitment process and generates real-world evidence (RWE) to advance the collective understanding of human health.---TriNetX---collaborates with the majority of industry leaders, including 13 of the top 15 pharmaceutical companies, and is powered by an impressive network of 170 healthcare organizations across 30 countries.---

As a result of its reach and rapidly expanding network,---TriNetX---has become the market leader in protocol design, feasibility and site selection. Researchers have leveraged the---TriNetX---network to analyze over 39,000 protocols, presented over 10,000 clinical trial opportunities to its healthcare members, and reduced site identification time in clinical trials by 50%.---

Currently, TriNetX healthcare organization members contribute access to a patient population of 400 million, representing over 40 billion clinical observations.--- With headquarters in Cambridge, Massachusetts, TriNetX is one of the fastest-growing, privately-held companies in the area's life sciences corridor.

What challenges we work on:---

TriNetX---is the global health research network that optimizes clinical research and enables discoveries through the creation of real-world evidence.---TriNetX---combines real-time access to longitudinal clinical data with state-of-the-art analytics to answer complex research questions at the speed of thought.--- Each member of our community shares in the consolidated value of our global, federated health research network that connects clinical researchers to the patient populations which they are attempting to study.---

Who we are looking for:------

Our customer base, networks, and product offerings are growing rapidly, and we are expanding our Clinical Sciences & Operations team with the hiring of an Analyst within the Clinical Study Feasibility & Analytics group. Reporting to the Manager of Clinical Study Feasibility & Analytics, the Analyst will serve the company as a clinical data subject matter expert and as a liaison between our clients and the TriNetX platform. Successful candidates in this position will work with Sales and Account Management teams representing clients in both industry and at the HCOs to assist users in finding relevant patient cohorts for clinical trials by translating clinical trial eligibility criteria into queries that can be run across the TriNetX Network.

The Analyst will need to draw upon their extensive expertise across the areas of clinical research and clinical trial design and execution to help our customers meet their goals. This role will support and educate users in a consultative manner, ultimately creating self-sufficient users of our platform and driving product adoption in the process. The ideal candidate is someone willing to learn our platform, data, and tools while utilizing existing clinical information and skills to discover new approaches in solving challenging matters.

Possible day-to-day:

  • Determine criteria that are most important for defining a patient cohort and formalize it using standard coding schemes for clinical data
  • Recognize nuances of clinical trial patient eligibility criteria and find creative ways of representing it using available clinical data sources
  • Work with external clients to identify, analyze and interpret data relevant to clinical questions and needs, and provide consultative assistance via written, oral, or in-person presentation methods
  • Answer client questions professionally and succinctly within a business day
  • Generate thorough and accurate clinical reports and summaries of data or results in a timely manner
  • Contribute to simultaneous customer engagements using effective workload management and prioritization capabilities
  • Collaborate with the Clinical Sciences & Operations staff and other teams across the company on project evaluation, data analysis for reports, presentations, and data requests as necessary
  • Provide feedback and suggestions for better product usability and new features to Product and Engineering teams within TriNetX
  • Serve as an internal subject matter expert and point of contact (e.g., by Medical Informatics, Sales, Marketing, Engineering) for query design/clinical information related questions
  • Support the sales and training processes of TriNetX on both the healthcare organization and sponsor (pharma/CRO) user ends of the platform
  • Review professional journals, health bulletins, and other publications to keep informed of current trends and new knowledge in the clinical research field as well as create scientific publications based on data and analysis from the TriNetX platform
  • Assure data quality, integrity, and confidentiality of information

    What you bring to the table:
    • Bachelor's degree in a health-related field or an equivalent combination of education and experience with preference to an advanced degree
    • 3+ years experience (5+ if remote) in healthcare, clinical research, clinical trial design or execution, feasibility, or patient recruitment, preferably in a pharma/CRO setting
    • Previous work in patient data including clinical information systems, EMR, claims, etc.
    • Strong familiarity with clinical data coding systems and/or computer-based clinical search tools and data analytics
    • Possess strong, flexible research skills and the ability to locate unusual information
    • Significant experience interacting with customers to gather and understand their business/technical/clinical needs and offer well-thought, data-driven solutions
    • Established ability to interpret and report analytical information in a clear concise manner with excellent communication skills on verbal, written, and presentation levels
    • Demonstrate time management and organization of workload to handle competing priorities and consistently meet deadlines
    • Attention to detail and thoroughness in all work output
    • Self-starter who can work independently as well as part of a diverse team

      Bonus points:
      • Have worked on TriNetX's platform
      • Have experience working in an HCO and/or CRO

        As a condition of employment, the individual must provide proof of Covid 19 vaccination unless a medical or religious exemption is granted by TriNetX.

        Learn more about TriNetX:

        Please feel free to check out our website

        Interested in joining our community?

        TriNetX is an Equal Opportunity Employer. All persons are considered for employment without regard to their race, color, creed, religion, national origin, ancestry, citizenship status, age, disability or handicap, sex or gender, marital status, sexual orientation, genetic information, gender identity, veteran status, or any other characteristic or status protected by applicable federal, state or local laws.

        TriNetX, US, requires all employees working in the United States to be vaccinated against Covid-19 in accordance with our company policy and following local, state, and federal guidelines.

        No recruiters or agencies, please. Any candidate(s) submitted through outside agencies will NOT be considered and disqualified. Thank You!

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Keywords: TriNetX, Irvine , Clinical Study Analyst, Remote US, Professions , Irvine, California

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