At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life – To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.
TrialMed is apremier global clinical site network, offering comprehensive services for clinical trials from early to latephases (Phase I toPhase IV). As a unified brand, TrialMed consolidates all clinical trial offerings under one global name, ensuring a seamless experience for stakeholders.
·Access to over 250 sites worldwide and apatient database of 20 million individuals, ensuring robust and diverse trial enrollments.
·Apatient-centric approach with capabilities for home trial services, allowingpatients toparticipate in clinical trials from their homes or communities.
·Comprehensive service offerings, including early development CRO services, consulting services, and clinicalpharmacology services.
Join TrialMed and bepart of a dynamic team dedicated to advancing medical research and improvingpatient care through innovative clinical
Are you passionate about improving patient’s lives for the better?
We are currently looking to recruit a Research Assistant for our Synexus Clinical Research site in Birmingham, United Kingdom
Working days, Monday to Friday, 37 hours a week, the main priority will always be patient safety. The research assistant provides lead administrative support to the research sites, executing and ensuring completion of all activities of the team by coordinating and assisting patients and visitors visiting the site. Acts as the firstline contact for patients and visitors. Ensures high standards of service and an outstanding patient experience in relation to communication, information and engagement with patients.
Key responsibilities for a Research Assistant are as follows:
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.
13. Assists with collating files, counting IP returns and ensuring compliance to company SOPs and COPs.
14. May assist with the education, evaluation, treatment and follow-up of sleep disorders for clinic patients.
15. Performs comprehensive sleep testing and analysis on clinic patients per study protocol.
16. Completes reimbursements of patient study expenses and payments ensuring standardized approach.
17. Ensures compliance with company quality framework, regulatory (GCP) legislation, guidelines and international standards (Global/Local COPS & SOPS).
To be considered for this exciting opportunity you will require the following skills and experience:
18. 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
19. Solid organizational skills and flexibility to manage workload and meet changing timelines
20. Firm attention to detail to ensure accuracy and efficiency in data entry
21. Solid interpersonal/customer service skills, positive attitude, and good oral and written communication
22. Capable of working in a team or independently
23. Solid English language and grammar skills
24. Good computer skills, including proficiency in MS Office (Word, Excel, and PowerPoint) and basic understanding of clinical trial database systems
25. Good analytical and data management skills to effectively analyze data/systems to ensure accuracy and efficiency
26. BLS or CPR certification
27. Ability to multi-task and ability to have oversight over a few studies with a number of participants simultaneously
28. Strong attention to detail
29. Working knowledge of medical terminology is an advantage
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we 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. #StartYourStory 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.