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Freelance Cra

2+ years
Not Disclosed
10 Sept. 27, 2024
Job Description
Job Type: 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

Freelance Clinical Research Associate - France

About Syneos Health

Syneos Health® is a leading integrated biopharmaceutical solutions organization focused on accelerating customer success. We translate clinical, medical affairs, and commercial insights into impactful outcomes, addressing the complexities of modern healthcare.

Our Clinical Development model places both customers and patients at the center of our work. We are committed to simplifying processes to enhance collaboration and drive the delivery of life-changing therapies.

Why Syneos Health?

  • Development Opportunities: We are dedicated to fostering professional growth through career development, supportive management, technical training, and peer recognition.

  • Inclusive Culture: Our Total Self culture encourages you to be your authentic self, creating a diverse environment where everyone feels they belong.

  • Global Impact: Join our team of 29,000 employees across 110 countries and discover how your work can make a difference.

Role Overview

As a Senior Clinical Research Associate I (SCRA I), you will oversee monitoring and site management for Phase I-IV clinical research projects. Your responsibilities will ensure that clinical trials are conducted according to protocols, standard operating procedures (SOPs), ICH-GCP guidelines, and all applicable local and federal regulations.

Key Responsibilities

  • Site Management: Conduct site qualification, initiation, interim monitoring, and close-out visits (both on-site and remotely) to ensure compliance with regulatory standards and protocols. Use your expertise to assess site performance, recommend actions, and escalate serious issues as necessary.

  • Informed Consent Verification: Ensure that the informed consent process is thoroughly executed and documented while safeguarding patient confidentiality and assessing factors affecting safety and data integrity.

  • Monitoring Activities: Execute tasks in line with the Clinical Monitoring/Site Management Plan (CMP/SMP), including:

    • Assessing site processes and conducting source document reviews.
    • Verifying the accuracy and completeness of clinical data in case report forms (CRFs).
    • Implementing query resolution techniques and guiding site staff to closure.
  • Investigational Product Oversight: Manage investigational product (IP) inventory, ensuring compliance with protocols for dispensing, labeling, and storage.

  • Documentation and Reporting: Maintain accurate records through confirmation letters, trip reports, and communication logs, while supporting patient recruitment and data tracking.

  • Project Coordination: Understand project scope, budgets, and timelines, ensuring site-level communications meet project objectives. Adapt quickly to changing priorities as necessary.

  • Liaison Role: Act as the primary contact with site personnel, ensuring training and compliance with project requirements.

  • Meeting Participation: Prepare for and attend Investigator Meetings and project staff meetings, and may lead discussions with supervision.

  • Audit Readiness: Provide guidance on audit preparedness and support necessary follow-up actions.

  • Mentorship: May train and mentor junior CRAs, providing guidance and oversight as needed.

  • Real World Late Phase (RWLP) Responsibilities: When acting as a Senior Site Management Associate I, support sites throughout the study lifecycle, conduct chart abstractions, and collaborate with local teams. Identify operational efficiencies and contribute to bid defense meetings.

Qualifications

  • Bachelor’s degree or RN in a related field, or equivalent combination of education and experience.
  • Strong knowledge of Good Clinical Practice/ICH Guidelines and applicable regulatory requirements.
  • Proficient computer skills with the ability to embrace new technologies.
  • Excellent communication, presentation, and interpersonal skills; basic critical thinking skills are expected.
  • Willingness to travel up to 75% regularly.

Get to Know Syneos Health

In the last five years, we have collaborated on 94% of all Novel FDA Approved Drugs and 95% of EMA Authorized Products, conducting over 200 studies across 73,000 sites with more than 675,000 trial patients. Join us in a dynamic and competitive environment and make a meaningful impact in the world of clinical research.