Research associate ii Work, Jobs in Radcliffe, Gtm (with Salaries)

Research Associate II
Thermo Fisher Scientific —Manchester
- 8 hour shift
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
5d
Clinical Research Associate II
IQVIA —Manchester
- No degree
1h
Graphic Designer II (12 Month FTC)
Fanatics (International) Limited —Manchester
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Graduate Associate - Technical Consultant 2026
Informed Solutions —Altrincham
- Full-time
- Hybrid work
- Analysis skills
- Presentation skills
- Software development
- Gym membership
- Referral programme
Quick apply
Senior Research Assistant (History and/or Philosophy of Science)
Manchester Metropolitan University —Manchester
- £33,002 a year
- Full-time
- Hybrid work
- Doctoral degree
- Communication skills
- Life insurance

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Clinical Research Associate II
IQVIA —Manchester
Requires at least 2 years on-site monitoring experience of interventional studies. Ensure copies/originals (as required) site documents are available for filing…
1h
Research Associate II
Thermo Fisher Scientific —Manchester
Performs non-technical procedures, including urine collection, subject walks and safety monitoring. Ability to access and use a variety of computer software…
5d

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research associate ii jobs near radcliffe, gtm

Research Associate II

Thermo Fisher Scientific -
Manchester

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Job details

Full-time
5 days ago

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Vital signs
Customer service
English
Microsoft Office
Analysis skills
Data management
Data entry
Organisational skills
Computer skills
Medical terminology
Communication skills
FDA regulations

Full job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Laboratory Setting, Office

Job Description

Provides general support to technical procedures with a range of complexity, including phlebotomy. Collects study-specific data by performing technical and non-technical procedures and interacting with patients. May also assist with the verification of patient data and collecting source documentation to complete the medical history. Monitors and ensures overall compliance at the site.

This position is full time, permanent onsite position.

May perform technical procedures running patient clinics including vital signs, Fibroscan, height, weight, Electrocardiogram etc.
Fully informs patients about the 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 the education, evaluation, treatment and follow-up of sleep disorders for clinic patients by following sleep laboratory operating procedures, applying electrodes and 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 study related 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, specimen labelling 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 COP’s, SOP’s, GCP and local regulations.
Provides training to new staff.
Note: Some tasks listed above only to be conducted as per country regulations and with relevant valid qualifications/ certification or supervision.

Knowledge, Skills and Abilities:

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 good working 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 written communication
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 basic understanding of clinical trial database systems
Strong analytical and data management skills to effectively analyze data/systems to ensure accuracy and efficiency Management Role: No management responsibility Working Conditions and Environment:
Work is performed in an office environment with exposure to electrical office equipment.
Occasional drives to site locations with occasional travel both domestic and international. Physical Requirements:
Frequently stationary for 6-8 hours per day.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
Frequent mobility required.
Occasional crouching, stooping, bending and twisting of upper body and neck.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
Frequently interacts with others to obtain or relate information to diverse groups.
Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.
Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.
Regular and consistent attendance.

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Refine Your Search

research associate ii jobs in radcliffe, gtm

Research Associate II

Clinical Research Associate II

Graphic Designer II (12 Month FTC)

Graduate Associate - Technical Consultant 2026

Senior Research Assistant (History and/or Philosophy of Science)

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