Research associate Work, Jobs in Salford (with Salaries)

CRA 2 - Single Sponsor Dedicated
IQVIA —Manchester
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Associate, Frontier Technology
Fitch Group —Manchester
- Azure
- AWS
- APIs
Associate Scientist
Cyprotex —Macclesfield
- Full-time
- Laboratory experience
- Master's degree
- Bachelor's degree
- Referral programme
Quick apply
5d
CRA2 - Multi-Sponsor Department
IQVIA —Manchester
- No degree
Evaluation Specialist: Associate / Associate Director
Steer —Manchester
- Full-time
- Hybrid work
- Management
- No degree
- Contracts
- Annual leave
- Employee assistance programme
Quick apply
Associate Principal Scientist – Peptide Development Chemistry - Pharmaceutical Sciences (PS)
AstraZeneca —Macclesfield
- Doctoral degree
- Master's degree
- Leadership
1d

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Research Scientist in Microsystems and Nanotechnology
University of Salford —Salford
Its activities are aligned with Greater Manchester’s Industrial Strategy priorities and focus on supporting SMEs and industrial partners through applied…
9d
Environmental Research Chemist (Organics)
Centre for Ecology & Hydrology —Lancaster
Q 2 - Give an example where you developed, adapted, or proposed a new organic analytical method to meet a scientific or project need.
£40,574 - £43,056 a year

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research associate jobs near salford

CRA 2 - Single Sponsor Dedicated

IQVIA -
Manchester

Apply Now

Job details

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Clinical research
English
Bachelor's degree
Computer skills
Financial management
Communication skills

Full job description

Join Us on Our Mission to Drive Healthcare Forward

IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.

Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications

Bachelor's Degree Degree in scientific discipline or health care preferred. Req
Requires at least 1 of year of on-site monitoring experience. Req
Equivalent combination of education, training and experience may be accepted in lieu of degree. Req
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Good therapeutic and protocol knowledge as provided in company training.
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
Written and verbal communication skills including good command of English language.
Organizational and problem-solving skills.
Effective time and financial management skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

*Please note - this role is not eligible for UK visa sponsorship*

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Apply Now

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research associate jobs in salford

CRA 2 - Single Sponsor Dedicated

Associate, Frontier Technology

Associate Scientist

CRA2 - Multi-Sponsor Department

Evaluation Specialist: Associate / Associate Director

Associate Principal Scientist – Peptide Development Chemistry - Pharmaceutical Sciences (PS)

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research associate jobs in salford

Associate, Frontier Technology

Associate Scientist

CRA2 - Multi-Sponsor Department

Evaluation Specialist: Associate / Associate Director

Associate Principal Scientist – Peptide Development Chemistry - Pharmaceutical Sciences (PS)

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I want to receive the latest job alerts for research associate in salford

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Associate Principal Scientist – Peptide Development Chemistry - Pharmaceutical Sciences (PS)