Research Associate II
Research Associate II
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Salary Not Disclosed
1 Vacancy
Job Description
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.)Job Description
Alongside clinical research through our PPD clinical research portfolio our work in Accelerated Enrollment Solutions optimizes each step of the patient journey in clinical trials such as securing sites and recruiting patients allowing for more patients to participate in clinical research. Your determination to put patients at the heart of every decision will improve health outcomes that people and communities depend on now and in the future.
Are you passionate about improving patients lives for the better
We are currentlylooking to recruita Research Associate II 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. Provides general support to technical procedures with a range of complexity including study-specific data by performing technical and non-technical procedures and interacting withpatients. May also assist with the verification of patient data and collecting source documentation tocomplete the medical history. Monitors and ensures overall compliance at the site.
Key responsibilities for a Research Associate are as follows:
- May perform technical procedures running patient clinics including vital signsFibroscan height weight Electrocardiogram etc. Fully informs patients aboutthe tests to be conducted and guides patients in the requirements of the trial.
- May perform Phlebotomy tests.
- Performs non-technical procedures including urine collection subject walks and
safety monitoring. - Under the general supervision of a licensed physician may conduct theeducation evaluation treatment and follow-up of sleep disorders for clinicpatients by following sleep laboratory operating procedures applying electrodesand sensors to ensure the collection of appropriate data of the sleep testing
process. - Prepares and calibrates equipment for testing to ensure proper functioning.
- Interacts regularly with patients during study visits in order to perform studyrelated procedures.
- Undertakes screening tests in accordance with protocol requirements.
- Assists in the lab sample processing and/or liaise with laboratories.
- Manages and/or completes ordering of clinical supplies.
- May assist with or oversee the maintenance of accurate freezer logs specimenlabelling and other documentation.
- May take consent if permitted according to country regulations.
- Reports Quality Incidents and participates in the investigation and resolution.
- Provides administrative support as needed.
- Ensures adherence to COPs SOPs GCP and local regulations.
- Provides training to new staff.
Note: Some tasks listed above only to be conducted as per country regulationsand with relevant valid qualifications/ certification or supervision.
To be considered for this exciting opportunity you will require the following skills and experience:
- Good medical terminology and ability to perform conducting of vital signs
- Strong understanding of Good Clinical Practices (GCP) with ability to learn and maintain a goodworking knowledge of FDA regulations and company/client SOPs and WPDs
- Strong organizational skills and flexibility to manage workload and meet changing timelines handling
multiple tasks efficiently and effectively - Thorough attention to detail to ensure accuracy and efficiency in data entry
- Strong interpersonal/customer service skills positive attitude and good oral and writtencommunication
- Capable of working in a team or independently
- Strong English language and grammar skills
- Strong computer skills including proficiency in MS Office (Word Excel and PowerPoint) and basicunderstanding of clinical trial database systems
- Strong analytical and data management skills to effectively analyze data/systems to ensure accuracy
and efficiency
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.
Required Experience:
IC
Employment Type
Full-Time
