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    Global Feasibility Specialist (Clinical Trials)

    Syneos Health
    0-1 years
    $47,000 to $80,000.
    Argentina Brazil Mexico Peru
    10 Jan. 22, 2025
    Job Description
    Job Type: Home Based Education: B.Sc,M.Sc,B.Pharma,M.Pharma,LifeScience Graduates Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Job Title: Global Feasibility Specialist (Clinical Trials)
    Location: Argentina/Brazil/Mexico/Peru (Home-Based)
    Job ID: 24006987
    Updated: January 18, 2025

    Company Overview:

    Syneos Health® is a leading fully integrated biopharmaceutical solutions organization committed to accelerating customer success. We work by translating clinical, medical affairs, and commercial insights into impactful outcomes. Our Clinical Development model centers around the customer and patient, consistently looking for ways to streamline work and improve how we operate.

    With 29,000 employees across 110 countries, Syneos Health offers a dynamic work environment where we foster diversity, inclusivity, and passion to change lives.

    Why Syneos Health:

    • Career Development: Passionate about developing employees through training, progression, and career growth opportunities.
    • Supportive Culture: A commitment to a “Total Self” culture, where you can authentically be yourself.
    • Diversity and Inclusion: We value a diverse workforce and provide an environment where everyone feels like they belong.

    Position Overview:

    The Global Feasibility Specialist (Clinical Trials) will assess the level of data required for RFPs and paid feasibility assessments, manage project assignments, and provide critical insights and data to support clinical trial feasibility. The role will involve liaising with internal stakeholders, conducting research, and ensuring effective communication with both internal and external stakeholders.

    Key Responsibilities:

    • Feasibility Assessments:
      • Assess data requirements for Requests for Proposals (RFPs) and paid feasibility assessments.
      • Under supervision, manage a limited number of project assignments of minimal to moderate complexity.
      • Respond to routine requests, applying knowledge and skills to data collection activities.
    • Research & Data Collection:
      • Conduct guided research of scientific literature, using internal and external sources, to prepare robust feasibility assessments.
      • Query clinical trial registry tools and other internal databases to support data collection.
    • Communication & Collaboration:
      • Collaborate with internal stakeholders to review sponsor requirements, protocols, and timelines for RFPs.
      • Build relationships with internal and external stakeholders, ensuring clear communication methods.
      • Maintain comprehensive records of work and store data in internal libraries in a timely manner.

    Qualifications:

    • Education:
      • BS/BA in Science, with an emphasis on medical research.
    • Experience & Skills:
      • Nominal experience in science or related fields.
      • Strong attention to detail in data analysis and presentation.
      • Flexible, creative, and self-motivated, with the ability to work independently and within a team.
      • Knowledge of scientific and clinical research data analysis methodologies.
      • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and internet research.
      • Strong organizational, interpersonal, and team-oriented skills.
      • Excellent time management and multitasking abilities.
    • Additional Skills:
      • Ability to be flexible and adapt to change.
      • Good communication skills, both verbal and written.
      • Must be flexible with travel and work hours, though travel is typically less than 5%.

    Compensation:

    • Base Salary:
      The annual base salary for this position ranges from $47,000 to $80,000. The actual salary will depend on the candidate's qualifications, skills, competencies, and proficiency for the role.

    About Syneos Health:

    • Over the past 5 years, Syneos Health has been involved in 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products, and over 200 studies across 73,000 sites with 675,000+ trial patients.

    Application Details:

    • Apply Now: [Application Link]
    • Join Our Talent Network: Stay connected to future career opportunities.

    Syneos Health is committed to building a diverse, inclusive, and authentic workplace. If your previous experience doesn’t align perfectly with the job description, we encourage you to apply anyway, as transferable skills are often considered.

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