Thermo Fisher Scientific
Patient Services Coordinator
Patient Services Coordinator at Thermo Fisher Scientific, based in Birmingham, West Midlands. This is a permanent role.
- Pay
- Not given by the employer
- Hours and contract
- Permanent · On site
- Location
- Birmingham, West Midlands
- Closing date
- Sector
- NHS Admin
Reference 637015344428352362
About the role
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
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 first line contact for patients and visitors. Ensures high standards of service and an outstanding patient experience in relation to communication information and engagement with patients.
Coordinates oversees and provides direction for the completion of administrative functions on assigned trials.
Welcomes patients and all visitors upon arrival at the site.
Completes data entry and visit completion information and manage the diary system ensuring data is accurate and up to date at all times.
Schedules patients for follow-up visits external appointments transport etc.
Conducts reminder telephone calls to patients to confirm visits.
Prepares all relevant patient documentation as per protocol and local regulations ahead of appointment.
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.
Collects and tracks patient notes lab results and questionnaires to facilitate prompt reviewing.
Assists with the collection of patient SDV from local medical professional.
Maintains a presentable safe and clean reception area to enhance the patient and visitor experience.
Completes or provides 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. 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.
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.
Completes reimbursements of patient study expenses and payments
Collaborates with other site functions to provide accurate and streamline processes and participate in best practice/process improvement initiatives
Accelerated Enrollment Solutions is a business unit of Pharmaceutical Product Development LLC a Delaware limited liability company (PPD)
collectively made up of Acurian Inc. and Synexus each a subsidiary of PPD.
ensuring standardized approach.
Ensures compliance with company quality framework regulatory (GCP) legislation guidelines and international standards (Global/Local COPS & SOPS).
Works on assignments that are semi-routine in nature but recognizes the need for occasional deviation from accepted practice.
Applies acquired job skills and company policies and procedures to complete assigned tasks.
Normally follows established procedures on routine work requires instructions only on new assignments.
High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification
Technical positions may require a certificate
Previous experience that provides the knowledge skills and abilities to perform the job (comparable to at least 2 years).
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 ability to have oversight over a few studies with a number of participants simultaneously
Strong attention to detail
Working knowledge of medical terminology is an advantage
Required Experience:
IC
Employment Type : Full-Time
Experience: years
Vacancy: 1
Reference: 637015344428352362 · Posted 1 day ago · Closes 12 Dec 2026 · Listed via Thermo Fisher Scientific
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