Research Assistant II

2 days ago


Liverpool, Liverpool, United Kingdom Thermo Fisher Scientific Full time
Job Title: Research Assistant II

At Thermo Fisher Scientific, we are seeking a highly motivated and organized Research Assistant II to join our team. As a Research Assistant II, you will play a critical role in supporting the conduct of clinical trials, ensuring the accuracy and integrity of data, and contributing to the success of our research initiatives.

Key Responsibilities:
  • Coordinate and oversee the completion of administrative functions on assigned trials, ensuring timely and accurate data entry and visit completion information.
  • Welcome patients and visitors upon arrival at the site, providing a positive and professional experience.
  • Manage the diary system, ensuring data is accurate and up-to-date at all times.
  • Schedule patients for follow-up visits, external appointments, and transport, as needed.
  • Conduct reminder telephone calls to patients to confirm visits.
  • Prepare all relevant patient documentation as per protocol and local regulations ahead of appointment.
  • 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.
  • Collect and track patient notes, lab results, and questionnaires to facilitate prompt reviewing.
  • Assist with the collection of patient SDV from local medical professionals.
  • Maintain a presentable, safe, and clean reception area to enhance the patient and visitor experience.
  • Complete or provide guidance to ensure completion of photocopying, faxing, postal activities, archiving, and patient refreshments.
  • May provide support in the Pharmacy in all areas of drug administration, assisting with deliveries, checking stock, and monitoring inventory of the dispensary.
  • May assist with the education, evaluation, treatment, and follow-up of sleep disorders for clinic patients, performing comprehensive sleep testing and analysis on clinic patients per study protocol.
  • Complete reimbursements of patient study expenses and payments.
  • Collaborate with other site functions to provide accurate and streamlined processes and participate in best practice/process improvement initiatives.
Requirements:
  • 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.
  • Solid organizational skills and flexibility to manage workload and meet changing timelines.
  • Firm attention to detail to ensure accuracy and efficiency in data entry.
  • Solid interpersonal/customer service skills, positive attitude, and good oral and written communication.
  • Capable of working in a team or independently.
  • Solid English language and grammar skills.
  • Good computer skills, including proficiency in MS Office (Word, Excel, and PowerPoint) and basic understanding of clinical trial database systems.
  • Good analytical and data management skills to effectively analyze data/systems to ensure accuracy and efficiency.
  • BLS or CPR certification.
  • Ability to multi-task and have oversight over a few studies with a number of participants simultaneously.
  • Strong attention to detail and working knowledge of medical terminology is an advantage.
Why Join Us:

At Thermo Fisher Scientific, we are committed to making the world healthier, cleaner, and safer. Our team of 100,000+ colleagues share a common set of values - Integrity, Intensity, Innovation, and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need. Join us and start your story with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds, and perspectives are valued.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does 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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