Research Assistant II
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Job Location:
Birmingham - UK
Monthly Salary:
Not Disclosed
Posted on:
30+ days ago
Vacancies:
1 Vacancy
Job Summary
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
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 patients lives for the better
We are currentlylooking to recruita 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 allactivities 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 patientexperience in relation to communication information and engagement with patients.
Key responsibilities for a Research Assistant are as follows:
- Coordinates oversees and provides direction for the completion of administrativefunctions on assigned trials.
- Welcomes patients and all visitors upon arrival at the site.
- Completes data entry and visit completion information and manage the diarysystem 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 regulationsahead of appointment.
- May collect medical history information for potential patients liaising withmedical facilities and networks to collect patient files documentation and otherrelevant information as may be required as per protocol.
- Collects and tracks patient notes lab results and questionnaires to facilitateprompt reviewing.
- Assists with the collection of patient SDV from local medical professional.
- Maintains a presentable safe and clean reception area to enhance the patientand visitor experience.
- Completes or provides guidance to ensure completion of photocopying faxingpostal activities archiving and patient refreshments.
- May provide support in the Pharmacy in all areas of drug administration. Assistswith deliveries checking stock and monitoring inventory of the dispensary.
- Assists with collating files counting IP returns and ensuring compliance tocompany SOPs and COPs.
- May assist with the education evaluation treatment and follow-up of sleepdisorders for clinic patients.
- Performs comprehensive sleep testing and analysison clinic patients per study protocol.
- Completes reimbursements of patient study expenses and payments ensuring standardized approach.
- 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:
- Good understanding of Good Clinical Practices (GCP) with ability to learn and maintain a goodworking 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 writtencommunication
- 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 basicunderstanding of clinical trial database systems
- Good analytical and data management skills to effectively analyze data/systems to ensure accuracyand efficiency
- BLS or CPR certification
- Ability to multi-task and ability to have oversight over a few studies with a number of participantssimultaneously
- Strong attention to detail
- 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 100000 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.
Key Skills
- Laboratory Experience
- Spss
- Data Collection
- DNA Isolation
- Stata
- Biochemistry
- Qualitative Research Interviewing
- Research Experience
- Statistical Software
- Molecular Biology
- Research Laboratory Experience
- Western Blot
About Company
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more
