Pharmaceutical Work, Jobs in Wilden, Bdf (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
3h
Senior Biological Scientist
Owlstone Medical Ltd —Cambridge
- Full-time
- Doctoral degree
- Master's degree
- In-person
- Free parking
- Health & wellbeing programme
Quick apply
13d
SPARK Trainee- UK
MoonLake Immunotherapeutics —Cambridge
- Hybrid work
- English
- In-person
- Communication skills
Quick apply
19h
Associate Analytical Chemist, Quality Control
Pharmaron —Rushden
- Laboratory experience
- Bachelor's degree
- Communication skills
Quick apply
Cell Culture Scientist
PerkinElmer —Stevenage
- Doctoral degree
- Data analysis skills
- Laboratory experience
- Annual leave
- Referral programme
1d
Medical Science Liaison - South England
Alexion Pharmaceuticals,Inc. —Cambridge
- Project management
- Bachelor's degree
- Travel
12d
Analytical Chemist, Quality Control
Pharmaron —Rushden
- Computer literacy
- Communication skills
- Time management
13d
Customer Support Specialist
Tanner Pharma Group —Redbourn
- £24,000 - £28,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health & wellbeing programme
- Sick pay
Quick apply
14d
Medical Device Regulatory and Quality Consultant
PA Consulting —Melbourn
- Full-time
- Annual leave
Quick apply
Clinical Science Specialist
MoonLake Immunotherapeutics —Cambridge
- Hybrid work
- Doctoral degree
- Master's degree
Quick apply
11d
Quality Manager
Healthxchange —Kettering
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Employee assistance programme
- Employee discount
Graduate Research Scientist- Bioanalysis LC-MS
Pharmaron —Rushden
- Laboratory experience
- Microsoft Office
- Bachelor's degree
Quick apply
Medical Science Liaison - South England
AstraZeneca —Cambridge
- Project management
- Bachelor's degree
- Travel
12d
R&D Quality Manager
Sandoz —Cambridge
- Full-time
- English
- Project management
- Agile
- Annual leave
Programme Lead – Pharmaceutical Drug Delivery Systems
TTP —Cambridge
- Full-time
- Travel
- Communication skills
- Life insurance
Quick apply
Sales Executive/Account Manager
Ginai Pharmaceuticals —St. Neots
- £25,000 a year
- Full-time
- Microsoft Powerpoint
- Sales
- Salesforce
Quick apply
14d
Quality Assurance Administrator
Hologic —Cambridge
- £32,000 - £40,000 a year
- Microsoft Powerpoint
- Microsoft Word
- Engineering
Scientific Communications and Engagement Lead
Cycle Pharmaceuticals —Cambridge
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Gym membership
- Flexible schedule
Digital Sales Lead Energy Industries - UK, Ireland and Azerbaijan
ABB Limited —Saint Neots
- Sales
- Annual leave
- Employee assistance programme
Quick apply
8d
Quality Manager
Mettler Toledo —Royston
- Data analysis skills
- SharePoint
- Annual leave

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pharmaceutical jobs near wilden, bdf

Clinical Trials Administrator -URGENT

Bliss Clinical Research
Bedford

Quick apply

Job details

Permanent | Full-time
£25,000 - £28,000 a year
3 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

pharmaceutical jobs in wilden, bdf

Clinical Trials Administrator -URGENT

Senior Biological Scientist

SPARK Trainee- UK

Associate Analytical Chemist, Quality Control

Cell Culture Scientist

Medical Science Liaison - South England

Analytical Chemist, Quality Control

Customer Support Specialist

Medical Device Regulatory and Quality Consultant

Clinical Science Specialist

Quality Manager

Graduate Research Scientist- Bioanalysis LC-MS

Medical Science Liaison - South England

R&D Quality Manager

Programme Lead – Pharmaceutical Drug Delivery Systems

Sales Executive/Account Manager

Quality Assurance Administrator

Scientific Communications and Engagement Lead

Digital Sales Lead Energy Industries - UK, Ireland and Azerbaijan

Quality Manager

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