Clinical trial Work, Jobs in Wavendon, Bkm (with Salaries)

Clinical Trials Administrator -URGENT
Bliss Clinical Research —Bedford
- £25,000 - £28,000 a year
- Full-time
- Patient monitoring
- Data analysis skills
- Analysis skills
- Work from home
Quick apply
9h
AAA Screening Programme Manager
Bedfordshire Hospitals NHS Foundation Trust —Bedford
- £49,387 - £56,515 a year
- Full-time
- Leadership
6d
Emergency Care Assistant - Milton Keynes
Ambulnz Community Partners —Milton Keynes
- £14.98 an hour
- Driving
- Employee assistance programme
Quick apply
Associate Analytical Chemist, Quality Control
Pharmaron —Rushden
- Laboratory experience
- Bachelor's degree
- Communication skills
Quick apply
Emergency First Responder - Milton Keynes
Ambulnz Community Partners —Milton Keynes
- £13.37 an hour
- Weekend availability
- Driving
Quick apply
Graduate Research Scientist- Bioanalysis LC-MS
Pharmaron —Rushden
- Laboratory experience
- Microsoft Office
- Bachelor's degree
Quick apply
Emergency Medical Technician - Milton Keynes
Ambulnz Community Partners —Milton Keynes
- £17.50 an hour
- Driving
- Employee assistance programme
Quick apply
Analytical Chemist, Quality Control
Pharmaron —Rushden
- Computer literacy
- Communication skills
- Time management
13d
Study Manager - 1 year FTC
Roche —Welwyn
- Hybrid work
- Bachelor's degree
2d
Principal Medical Writer
GlaxoSmithKline —Stevenage
- £118,000 - £168,000 a year
- Full-time
- Hybrid work
- Doctoral degree
- English
- In-person
Senior Medical Science Liaison
Merz Aesthetics UK Ltd. —Hemel Hempstead
- Doctoral degree
- Sales
- Microsoft Office
Quick apply
Paramedic - Milton Keynes
Ambulnz Community Partners —Milton Keynes
- £25 - £29 an hour
- Driving
- Employee assistance programme
Quick apply
Registered Nurse-Research and Development
East and North Hertfordshire Teaching NHS Trust —Stevenage
- £31,049 - £37,796 a year
- Full-time
- Flexible schedule
2d
LTO Regulatory Partner
Roche —Welwyn
- Bachelor's degree
- Mentoring
Programming Leader
GlaxoSmithKline —Stevenage
- Full-time
- Hybrid work
- Driving
- Quality control
- In-person
6d
Director, Research, Ethics and policy
AHRO Center for Academic Research —Stevenage
- £30,536.94 - £42,263.45 a year
- Full-time
- Laboratory experience
- Supervising experience
- Project management
Quick apply
Senior Analytical Chemist, Quality Control
Pharmaron —Rushden
- Analysis skills
- Communication skills
- Time management
12d
Pharmacy Technician
Northampton General Hospital NHS Trust —Northampton
- £28,392 - £31,157 a year
- Full-time
- Hospital
8d
Medical Director, Clinical Development, Hepatology
GlaxoSmithKline —Stevenage
- £202,500 - £371,250 a year
- Full-time
- Annual leave
Professional Lead Product Developer
Medik8 —Aylesbury
- £60,000 - £70,000 a year
- Hybrid work
- Master's degree
- Project management
- Presentation skills
- Employee discount
Quick apply

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Clinical Trials Administrator -URGENT

Bliss Clinical Research
Bedford

Quick apply

Job details

Permanent | Full-time
£25,000 - £28,000 a year
9 hours ago

Benefits

Company pension
Work from home
On-site parking

Qualifications

Statistical software
Clinical research
Patient monitoring
Phlebotomy
Data analysis skills
Analysis skills
Supervising experience
Compliance management
Data management
Medical terminology
FDA regulations
Nursing

Full job description

Job Overview
We are seeking a highly organised and detail-oriented Clinical Trial Administrator to oversee and coordinate clinical research projects within our organisation. The successful candidate will be responsible for ensuring compliance with regulatory standards, managing trial operations, and supervising research staff. This role offers an excellent opportunity for professionals with a strong background in clinical research, nursing, or related fields to contribute to innovative healthcare solutions. The position is paid and requires a proactive approach to managing multiple aspects of clinical trials from initiation to completion.

Duties

Organizing investigator site files, scheduling participant visits, tracking enrollment, and ensuring that data is accurately collected, entered, and stored.
Support clinical operations by coordinating with investigators, site staff, sponsors, and external partners to facilitate smooth day-to-day trial activities.
Plan, organise, and oversee all phases of clinical trials in accordance with FDA regulations and Good Clinical Practice (GCP) guidelines.
Coordinate with cross-functional teams, including medical staff, data managers, and regulatory bodies to ensure trial progress aligns with project timelines.
Monitor patient safety and well-being throughout the trial period, including patient monitoring and phlebotomy procedures when necessary.
Ensure accurate data management by overseeing data collection, entry, and analysis using statistical software.
Maintain compliance with all regulatory requirements, including documentation and reporting obligations.
Supervise clinical research staff, providing guidance on protocol adherence, training, and performance management.
Review trial protocols, consent forms, and other documentation for accuracy and compliance.
Liaise with external partners such as laboratories, vendors, and regulatory agencies to facilitate smooth trial operations.

Skills

Strong knowledge of medical terminology and clinical research methodologies.
Excellent analysis skills for interpreting complex data sets and trial results.
Proficiency in statistical software used for data analysis in clinical research.
In-depth understanding of FDA regulations and compliance management within clinical trials.
Experience in patient monitoring techniques, including phlebotomy if applicable.
Proven supervisory experience leading multidisciplinary teams in a clinical setting.
Background in nursing or healthcare professions is highly desirable.
Effective data management skills ensure the accuracy and integrity of trial information.
Ability to manage multiple projects simultaneously while maintaining attention to detail. This role offers a dynamic environment for dedicated professionals eager to advance healthcare through meticulous research management. Applicants should demonstrate a comprehensive understanding of clinical trial processes combined with strong leadership capabilities to succeed in this position.
Ability to work on-site in Bedford, collaborate effectively with clinical staff, and adapt to a fast-paced research environment.
Prior experience in a clinical research setting or exposure to NHS or pharmaceutical environments is an advantage.

Pay: £25,000.00-£28,000.00 per year

Benefits:

Company pension
On-site parking
Work from home

Ability to commute/relocate:

Bedford MK40 2FG: reliably commute or plan to relocate before starting work (required)

Location:

Bedford MK40 2FG (preferred)

Work Location: In person

Quick apply

Refine Your Search

clinical trial jobs in wavendon, bkm

Clinical Trials Administrator -URGENT

AAA Screening Programme Manager

Emergency Care Assistant - Milton Keynes

Associate Analytical Chemist, Quality Control

Emergency First Responder - Milton Keynes

Graduate Research Scientist- Bioanalysis LC-MS

Emergency Medical Technician - Milton Keynes

Analytical Chemist, Quality Control

Study Manager - 1 year FTC

Principal Medical Writer

Senior Medical Science Liaison

Paramedic - Milton Keynes

Registered Nurse-Research and Development

LTO Regulatory Partner

Programming Leader

Director, Research, Ethics and policy

Senior Analytical Chemist, Quality Control

Pharmacy Technician

Medical Director, Clinical Development, Hepatology

Professional Lead Product Developer

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