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Cra Ii (Cz) - Sponsor-Dedicated

2+ years
Not Disclosed
10 Dec. 5, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Here’s a refined and structured version of the Clinical Research Associate II job description:


Position: Clinical Research Associate II
Company: Syneos Health®
Location: Remote (Global)

About Syneos Health®
Syneos Health is a global leader in fully integrated biopharmaceutical solutions. We drive customer success by translating clinical, medical, and commercial insights into innovative outcomes that meet today’s market demands.

Our Clinical Development model prioritizes the customer and patient experience, simplifying processes to foster collaboration and efficiency. Join a team of over 29,000 professionals across 110 countries, working to change lives by accelerating the delivery of life-saving therapies.

Why Syneos Health?

  • Career Development: Grow through technical training, peer recognition, and mentorship opportunities.
  • Inclusive Culture: Be your authentic self in our Total Self culture that celebrates diversity of thoughts, backgrounds, and perspectives.
  • Collaboration and Innovation: Work with passionate problem solvers committed to building a company that everyone loves to work for.

Job Responsibilities
As a Clinical Research Associate II, you will:

  • Perform site qualification, initiation, interim monitoring, site management, and close-out visits (on-site or remote).
  • Evaluate site and staff performance, ensuring adherence to ICH-GCP, Good Pharmacoepidemiology Practice (GPP), regulatory standards, and company SOPs.
  • Verify informed consent processes, protecting subject confidentiality and data integrity.
  • Identify protocol deviations, safety concerns, and pharmacovigilance issues at investigator sites.

Core Responsibilities

  • Conduct Source Document Review and verify clinical data accuracy in case report forms (CRFs).
  • Utilize hardware/software to support data review and capture, ensuring site compliance with electronic data requirements.
  • Oversee investigational product (IP) inventory, reconciliation, storage, and administration compliance.
  • Regularly review the Investigator Site File (ISF) for accuracy, ensuring alignment with the Trial Master File (TMF).
  • Document site activities through confirmation letters, trip reports, communication logs, and follow-ups.
  • Support subject recruitment, retention, and awareness strategies.
  • Provide site-level guidance for audit readiness and address follow-up actions post-audit.
  • Act as a primary liaison with study site personnel or collaborate with Central Monitoring Associates.

Real World Late Phase (RWLP) Additional Responsibilities

  • Provide site support throughout the study lifecycle, from site identification to close-out.
  • Conduct chart abstraction and data collection.
  • Collaborate with sponsor affiliates, medical science liaisons, and local country staff.
  • Train junior staff and suggest potential sites based on treatment patterns and healthcare provider (HCP) associations.

Qualifications

  • Bachelor’s degree or RN in a related field (or equivalent combination of education and experience).
  • Strong knowledge of Good Clinical Practice (GCP), ICH guidelines, and relevant regulations.
  • Proficiency with computer systems and willingness to adopt new technologies.
  • Excellent communication, presentation, and interpersonal skills.
  • Ability to travel up to 75% as required.

Why Join Syneos Health?

  • Over the past 5 years, Syneos Health has worked on:
    • 94% of all FDA-approved novel drugs.
    • 95% of EMA-authorized products.
    • 200+ studies across 73,000 sites and 675,000+ trial patients.

Additional Information
This job description is not exhaustive and may be adjusted based on organizational needs. Syneos Health is committed to creating an inclusive environment, complying with global regulations, and offering reasonable accommodations under the Americans with Disabilities Act (ADA).

Apply Now


This streamlined version enhances readability while maintaining critical details. Let me know if additional changes are needed!