Instagram
youtube
Facebook

Clinical Trial Coord Ii

2+ years
Not Disclosed
10 Sept. 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

Work Schedule:
Standard (Mon-Fri)

Environmental Conditions:
Office-based

Job Description:

Make a Global Impact:
Join Thermo Fisher Scientific Inc., a global leader in scientific research, as a Clinical Trial Coordinator Level I. We are seeking a dedicated individual with a passion for supporting clinical research to join our Clinical Operations team. In this role, you will provide essential administrative and technical support for clinical trials, helping ensure the success of high-quality, cost-efficient clinical studies from start-up to close-out. Collaborating with top professionals, you’ll play a key role in advancing impactful clinical programs.

Key Responsibilities:

  • Provide comprehensive administrative and technical support to the Project Team.
  • Ensure audit readiness by conducting file reviews per SOPs and department guidelines.
  • Assist with site activation activities and develop strategies for quick site activations.
  • Collaborate with investigators and site personnel to assess study feasibility.
  • Develop and review site lists based on strategic needs and input from local teams.
  • Support the training of new staff and participate in departmental process improvement initiatives.

Requirements:

  • Bachelor’s degree in life sciences or pharmacy.
  • Minimum of 2 years of relevant experience or an equivalent combination of education, training, and related experience.
  • Strong organizational skills, attention to detail, and ability to manage multiple tasks efficiently.
  • Proven ability to analyze project-specific data and systems for accuracy.
  • Strong communication skills, with the ability to collaborate effectively with team members and external stakeholders.
  • Proficiency in MS Office (Word, Excel, PowerPoint) and ability to learn clinical trial database systems.
  • Good understanding of country-specific regulations, ICH Good Clinical Practices, and SOPs relevant to clinical project implementation.

Why Join Us:
At Thermo Fisher Scientific, we are committed to making the world healthier, cleaner, and safer. We value diversity and inclusion and are proud to offer reasonable accommodations for individuals with disabilities during the application process. If you are passionate about making a meaningful impact in the world of clinical research, apply today and be part of our mission.

Apply now: http://jobs.thermofisher.com