Instagram
youtube
Facebook

Internship - In House Cra/Study Start-Up -12 Months- Maidenhead (Office-Based)

0-2 years
Preferred by Comapny
11 Nov. 25, 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

Job Title: Global Internship Program – Clinical Operations Intern
Location: Maidenhead, United Kingdom
Time Type: Full-Time

About Fortrea

Fortrea is a leading global contract research organization (CRO) that blends decades of experience with innovation to deliver comprehensive clinical development and commercialization services for biopharmaceutical products. Operating in over 90 countries, we partner with emerging and established biopharma, medical device, and diagnostic companies to advance healthcare and improve lives worldwide.

About the Internship

Join the Fortrea 2025 Global Internship Program, an exciting opportunity for Life Science students to gain hands-on experience in the clinical research industry. As an intern, you’ll play a pivotal role in the setup, execution, and closure of clinical trials in the UK and Ireland. You’ll gain valuable insight into clinical operations and startup processes, working alongside seasoned professionals in a fast-paced and dynamic environment.

Responsibilities

  • Serve as the primary contact for hospital sites and staff (Investigators, Doctors, Nurses, Trial Coordinators) to address queries related to clinical trial protocols.
  • Collaborate with Clinical Research Associates and Start-Up Specialists to collect missing documents and monitor patient status.
  • Conduct initial outreach and feasibility studies for potential clinical trials.
  • Process amendments for clinical trial protocols by submitting to regulatory authorities (e.g., MHRA) and ethics committees.
  • Review and update study progress reports to ensure all tasks are completed.
  • Audit electronic Case Report Forms to identify and correct missing or inaccurate data.
  • Manage clinical trial supplies to ensure seamless patient visits.
  • Assist with trial operations, potentially including accompanied visits to hospital sites.

Qualifications

  • Currently pursuing a Bachelor’s degree in Life Sciences.
  • Strong teamwork and autonomous working capabilities.
  • Excellent organizational and communication skills.
  • Experience from a prior placement year in a related industry is desirable.
  • Willingness to relocate to Maidenhead for the 12-month internship if not local.

Why Join Fortrea?

  • Gain exposure to real-world clinical research processes in a collaborative and innovative environment.
  • Develop professional skills through dedicated training and workshops designed to support your scientific career aspirations.
  • Participate in philanthropic projects and network with senior management and mentors.
  • Contribute to impactful projects that help deliver life-changing therapies to patients worldwide.

Benefits

  • Experience working in one of the world’s leading CROs.
  • Training programs tailored to foster professional development.
  • Opportunities to collaborate on meaningful projects that make a global impact.

Equal Opportunity Employer

Fortrea is committed to fostering a diverse and inclusive workplace. We do not discriminate based on race, religion, color, national origin, gender, age, veteran status, disability, or other legally protected characteristics.

For more information, visit www.fortrea.com.

Application Deadline: Rolling applications; positions fill quickly—apply early!