Research Coordinator

2 days ago

Cardiff, Cardiff, United Kingdom Thermo Fisher Scientific Full time

Key Responsibilities for a Research Assistant II:

  1. Coordinates, oversees and provides direction for the completion of administrative functions on assigned trials.
  2. Welcomes patients and all visitors upon arrival at the site.
  3. Completes data entry and visit completion information and manage the diary system, ensuring data is accurate and up to date at all times.
  4. Schedules patients for follow-up visits, external appointments, transport, etc.
  5. Conducts reminder telephone calls to patients to confirm visits.
  6. Prepares all relevant patient documentation as per protocol and local regulations ahead of appointment.
  7. May collect medical history information for potential patients, liaising with medical facilities and networks to collect patient files, documentation and other relevant information as may be required as per protocol.
  8. Collects and tracks patient notes, lab results and questionnaires to facilitate prompt reviewing.
  9. Assists with the collection of patient SDV from local medical professional.
  10. Maintains a presentable, safe and clean reception area to enhance the patient and visitor experience.
  11. Completes or provides guidance to ensure completion of photocopying, faxing, postal activities, archiving and patient refreshments.
  12. May provide support in the Pharmacy in all areas of drug administration. Assists with deliveries, checking stock and monitoring inventory of the dispensary. Assists with collating files, counting IP returns and ensuring compliance to company SOPs and COPs.
  13. May assist with the education, evaluation, treatment and follow-up of sleep disorders for clinic patients. Performs comprehensive sleep testing and analysis on clinic patients per study protocol.
  14. Completes reimbursements of patient study expenses and payments
  15. Collaborates with other site functions to provide accurate and streamline processes and participate in best practice/process improvement initiatives

Knowledge, Skills and Abilities:

  1. Good understanding of Good Clinical Practices (GCP), with ability to learn and maintain a good working knowledge of FDA regulations and company/client SOPs and WPDs
  2. Solid organizational skills and flexibility to manage workload and meet changing timelines
  3. Firm attention to detail to ensure accuracy and efficiency in data entry
  4. Solid interpersonal/customer service skills, positive attitude, and good oral and written communication
  5. Capable of working in a team or independently
  6. Solid English language and grammar skills
  7. Good computer skills, including proficiency in MS Office (Word, Excel, and PowerPoint) and basic understanding of clinical trial database systems
  8. Good analytical and data management skills to effectively analyze data/systems to ensure accuracy and efficiency
  9. BLS or CPR certification
  10. Ability to multi-task and ability to have oversight over a few studies with a number of participants simultaneously
  11. Strong attention to detail Working knowledge of medical terminology is an advantage

About Thermo Fisher Scientific:

We are a global leader in the life sciences, serving customers in healthcare, academia, government, and industry, delivering innovative solutions to help push the boundaries of human understanding and improve the human condition. Our Mission is to enable our customers to make the world healthier, cleaner and safer.

Our Values:

  1. Integrity: We act with integrity, honesty, and transparency in all our interactions.
  2. Intensity: We strive for excellence in everything we do, and we achieve it through our passion, dedication, and perseverance.
  3. Innovation: We foster a culture of innovation, where curiosity and creativity drive new ideas and solutions.
  4. Involvement: We empower our employees to make a meaningful impact through their contributions, and we recognize and reward their achievements.

We are an EEO/Affirmative Action Employer and do not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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