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Sponsor Dedicated Cra Ii/ Sr Cra - Home Based Ita

2+ years
Not Disclosed
10 Oct. 21, 2024
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Sponsor Dedicated CRA II/Sr CRA - Home Based ITA

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. We leverage unique clinical, medical affairs, and commercial insights to address modern market challenges.

Our Clinical Development model centers on the customer and patient. We constantly strive to simplify and streamline processes, ensuring that Syneos Health is easy to collaborate with and work for.

Whether in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and committed to accelerating the delivery of therapies, driven by our passion for changing lives.

Discover what our 29,000 employees across 110 countries already know: WORK HERE MATTERS EVERYWHERE.

Why Syneos Health

We are dedicated to developing our people through career growth opportunities, supportive management, technical training, peer recognition, and a comprehensive rewards program. Our Total Self culture allows you to be your authentic self, creating an inclusive environment where everyone belongs.

Job Responsibilities

  • Conduct site qualification, initiation, interim monitoring, site management, and close-out visits (on-site or remotely) to ensure compliance with regulatory standards, ICH-GCP, and study protocols. Evaluate site performance and escalate serious issues as necessary, developing action plans accordingly.

  • Verify the informed consent process for each subject/patient, ensuring confidentiality and assessing factors that may affect safety and data integrity at investigator sites.

  • Execute the Clinical Monitoring/Site Management Plan (CMP/SMP) by:

    • Assessing site processes.
    • Conducting Source Document Reviews and verifying data accuracy in case report forms (CRFs).
    • Applying query resolution techniques and guiding site staff as needed.
    • Ensuring compliance with electronic data capture requirements.
  • Manage investigational product (IP) inventory, ensuring proper dispensing and administration according to protocols. Address issues related to blinded or randomized information.

  • Regularly review the Investigator Site File (ISF) for accuracy and completeness, reconciling it with the Trial Master File (TMF) and ensuring compliance with archiving requirements.

  • Document activities through confirmation letters, trip reports, and other necessary project documents. Support subject/patient recruitment and retention strategies.

  • Understand project scope, budgets, and timelines for assigned activities, ensuring site-level communication meets project objectives.

  • Act as a primary liaison with study site personnel and ensure compliance with training requirements.

  • Prepare for and participate in Investigator Meetings, sponsor meetings, and clinical training sessions.

  • Provide guidance for audit readiness at the site and project levels and support preparation for audits.

  • Maintain up-to-date knowledge of ICH/GCP Guidelines and company SOPs, completing required training.

  • For Real World Late Phase studies, the CRA II will use the title of Site Management Associate II, with additional responsibilities including:

    • Supporting sites throughout the study lifecycle from identification to close-out.
    • Knowledge of local requirements for real-world late-phase study designs.
    • Conducting chart abstraction and data collection.
    • Collaborating with Sponsor affiliates and local staff.
    • Identifying out-of-scope activities and suggesting potential sites based on local knowledge.

Qualifications

What We’re Looking For:

  • Minimum of 2 years as a certified CRA, in accordance with M.D. 15 Nov 2011.
  • Knowledge of Good Clinical Practice/ICH Guidelines and relevant regulatory requirements.
  • Proficient computer skills and ability to adapt to new technologies.
  • Excellent communication, presentation, and interpersonal skills.
  • Willingness to travel up to 75% of the time.

Get to Know Syneos Health

In the past five years, we've collaborated on 94% of all Novel FDA Approved Drugs and 95% of EMA Authorized Products, conducting over 200 studies across 73,000 sites and 675,000+ trial patients. Join us in taking initiative and challenging the status quo in a dynamic environment.

Additional Information:

The tasks and responsibilities outlined in this job description are not exhaustive. The company may assign additional tasks at its discretion. Equivalent experience, skills, and education will be considered. This document does not constitute an employment contract.