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Senior Cra Belgium

2+ years
Not Disclosed
10 Nov. 11, 2024
Job Description
Job Type: Full Time 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

Job Title: Senior Clinical Research Associate (CRA)

Location: Belgium
Company: Syneos Health


Company Overview:

Syneos Health® is a leading, fully integrated biopharmaceutical solutions organization that accelerates customer success by translating clinical, medical affairs, and commercial insights into actionable outcomes. Our goal is to simplify and streamline processes while keeping the customer and patient at the center of everything we do. Join us as we innovate, collaborate, and deliver life-changing therapies.


Position Overview:

We are seeking an experienced Senior Clinical Research Associate (CRA) to join our Belgian team. In this role, you will ensure the compliance, safety, and efficiency of clinical trials by performing site qualification, initiation, monitoring, and close-out visits. You will work closely with the clinical team and site personnel to ensure all aspects of the trial are executed effectively, in line with regulatory requirements, ICH-GCP guidelines, and protocol specifications.


Key Responsibilities:

  • Site Monitoring & Management:
    Perform site qualification, initiation, monitoring, and close-out visits (either on-site or remotely). Evaluate the performance of study sites and staff, provide recommendations, and address any issues by developing action plans in collaboration with the project team.

  • Regulatory Compliance:
    Ensure all activities are compliant with ICH-GCP, GPP, and applicable regulatory guidelines. Review informed consent procedures and confirm the confidentiality of patient data. Identify and address issues affecting patient safety and clinical data integrity.

  • Data Review & Source Documentation:
    Conduct Source Document Review (SDR) and Source Data Verification (SDV) to ensure clinical data accuracy. Resolve any discrepancies or queries through effective communication with site staff, ensuring compliance with electronic data capture and clinical data entry requirements.

  • Investigational Product (IP) Management:
    Oversee IP inventory, reconciliation, storage, and security. Ensure investigational product is dispensed and administered per protocol, and resolve any issues related to blinded or randomized information.

  • Site File Maintenance:
    Regularly review the Investigator Site File (ISF) for completeness, accuracy, and timeliness, ensuring it aligns with the Trial Master File (TMF). Support sites with archiving essential documents according to local guidelines and regulations.

  • Training & Mentorship:
    Provide guidance to junior CRAs and assist in their training and sign-off visits. Support site staff training on study requirements and audit readiness.

  • Project Management:
    Ensure project scope, timelines, and budgets are met by managing site-level activities and communications. Adapt to changing priorities to ensure the successful delivery of clinical study goals.

  • Collaboration & Meetings:
    Collaborate with project site personnel and participate in Investigator Meetings, Sponsor meetings, and global clinical monitoring project staff meetings. Provide audit readiness support and prepare for audits and follow-up actions.


Qualifications:

  • Education:
    Bachelor’s degree or RN in a related field, or equivalent combination of education, training, and experience.

  • Experience:

    • At least 3+ years of experience as a Clinical Research Associate (CRA), with a solid track record in monitoring clinical trials.
    • Previous monitoring experience in Belgium is highly preferred.
    • Experience in rare diseases and/or immuno-neuropathy is a plus.
  • Skills & Competencies:

    • Strong knowledge of Good Clinical Practice (GCP), ICH guidelines, and other regulatory requirements.
    • Proficiency in Dutch, French, and English (fluency required).
    • Strong computer skills and adaptability to new technologies.
    • Excellent communication, presentation, and interpersonal skills.
    • Ability to manage required travel for monitoring visits throughout Belgium.

Why Syneos Health?

At Syneos Health, we’re driven to accelerate the delivery of therapies that change lives. We are passionate about developing our people and creating a diverse, inclusive culture where everyone feels like they belong. With our global reach, we offer a collaborative and dynamic work environment that allows you to thrive both personally and professionally.

  • Employee Development: Career growth opportunities through training, mentorship, and career progression programs.
  • Total Self Culture: A supportive environment where you can bring your authentic self to work.
  • Recognition & Rewards: Competitive salaries, peer recognition, and a comprehensive total rewards program.

Additional Information:

Tasks, duties, and responsibilities in this job description are not exhaustive. The company may assign additional tasks at its discretion. We are committed to compliance with all applicable laws, including the EU Equality Directive, the Americans with Disabilities Act, and other regulations related to recruitment and employment.