Clinical data manager Work, Jobs in Scotland (with Salaries)

Clinical Data Manager
Charles River Laboratories —Tranent
- Up to £40,000 a year
- Full-time
- Computer literacy
- Bachelor's degree
- Organisational skills
9d
Clinical Advisor - Assistant Manager, Wellness Advisory Team
Deloitte —Aberdeen
- Hybrid work
- Bachelor's degree
- Continuous improvement
- Case management
13d
Health Information Manager
LCM Healthcare Services Ltd —Hamilton
- £48,000 - £55,000 a year
- Full-time
- Data analysis skills
- Analysis skills
- In-person
- Health & wellbeing programme
- Annual leave
Quick apply
5d
Services & Delivery Manager
Ewen's Room —Fort William
- £36,000 - £40,000 a year
- Part-time
- Hybrid work
- Management
- No degree
- Organisational skills
Quick apply
9d
Healthcare Scientist Associate Practitioner - Laboratory Medicine
NHS Scotland —Glasgow
- £31,537 - £34,303 a year
- Full-time
- Management
- Computer literacy
- Laboratory experience
- Annual leave
- Employee assistance programme
3d
Clinical Project Manager x 2
Charles River Laboratories —Tranent
- £35,000 - £40,000 a year
- Full-time
- Master's degree
- Bachelor's degree
- Travel
2d
Part-time Chief Executive Officer (CEO)
HSTAR Scotland SCIO —Stirling
- £30,400 a year
- Part-time
- Microsoft Word
- Microsoft Outlook
- Management
- Health & wellbeing programme
- Annual leave
Quick apply
Operations Manager
Anatomical Concepts UK Ltd —Glasgow
- £37,000 - £44,000 a year
- Full-time
- Continuous improvement
- Team management
- Contracts
- Free parking
- Gym membership
Quick apply
4d
Clinical Manager - Staff Bank
NHS Scotland —Kirkcaldy
- £65,125 - £70,303 a year
- Call to connect
- Microsoft Office
- Master's degree
- Analysis skills
11d
Data Manager – West of Scotland Safe Haven
NHS Scotland —Glasgow
- £52,845 - £61,466 a year
- Full-time
- Analysis skills
- Analytics
- Annual leave
- Employee assistance programme
10d
Healthcare Development Manager
IQVIA —Glasgow
- Full-time
- Hybrid work
- No degree
- Communication skills
12d
Territory Manager - Scotland
Dental Direct UK Ltd —Scotland
- Full-time
- Hybrid work
- Microsoft Word
- CRM software
- Google Suite
Quick apply
Medical Writer - Publications
Real Chemistry —Edinburgh
- Hybrid work
- Microsoft Powerpoint
- Doctoral degree
- Master's degree
- Annual leave
Hub Manager (Edinburgh)
Duncan & Todd Opticians —Scotland
- From £40,000 a year
- Full-time
- Customer service
- Data analysis skills
- Analysis skills
- Store discount
- Employee discount
Quick apply
4d
R & D Scientist (Haematology)
AliveDx —Penicuik
- Full-time
- Data analysis skills
- Laboratory experience
- No degree
Senior HR Business Partner
IQVIA —Livingston
- Full-time
- Hybrid work
- Microsoft Office
- Presentation skills
- Bachelor's degree
Head of Programme – Psychology Specialist Practice
NHS Scotland —Balloch
- £90,808 - £97,338 a year
- Full-time
- Hybrid work
- Research
- Training & development
- Leadership
- Annual leave
3d
Project Financial Analyst 2
IQVIA —Livingston
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- Continuous improvement
- Work from home
11d
Suicide Prevention Officer
Change Mental Health —Edinburgh
- £30,768.10 a year
- Part-time
- Hybrid work
- Supervising experience
- Project management
- Travel
- Employee assistance programme
- Employee discount
Quick apply
Medical Records Summariser/Workflow Administrator
Ladywell Medical Centre East —Edinburgh
- From £27,061 a year
- Part-time
- Hybrid work
- Microsoft Excel
- SQL
- Analysis skills
- Free parking
- Store discount
Quick apply
10d

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clinical data manager jobs near scotland

Clinical Data Manager

Charles River Laboratories -
Tranent

Apply Now

Job details

Full-time
Up to £40,000 a year
9 days ago

Qualifications

Clinical research
Computer literacy
Stakeholder liaison
Microsoft Office Suite
Bachelor's degree
Organisational skills
Computer skills
Training & development
Pharmaceutical industry setting experience
Leadership
Communication skills
FDA regulations

Full job description

Req ID #: 235190
Tranent, Scotland, GB
1st
Full time

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Overview

Do you have expertise in and a passion for Clinical Data Management?

Have you got the desire to improve health and lives?

Charles River Laboratories are excited to be recruiting for a Clinical Data Manager as part of our Clinical Support Services function, working remotely (within the UK only) to effectively manage varying levels of complex clinical trial data across multiple assigned projects within Safety Assessment.

As Clinical Data Manager, you’ll be ensuring that all data is reported accurately and within the set timelines as per the driving documents and standards. You will be utilise a deep understanding of working to CDISC SDTM data standards, coupled with being able to demonstrate outstanding customer service skills to coordinate Safety Assessment site operations and clients throughout the clinical data life cycle.

Job Description

What you’ll be doing:

Request requirements from the sponsor for transfer frequency and dataset architecture for data transferred to sponsors in support of clinical study work.
Prepare and/or review Data Transfer Agreements for all assay data types of any complexity.
Oversee preparation of the Study Data Tabulation Model (SDTM) and non-SDTM datasets for a clinical study.
Perform quality control on all aspects of the clinical study as appropriate, to include, but not be limited to clinical regulatory compliance, Data Transfer Agreements, creation of clinical programming specifications, review of external client(s) clinical study documentation, review and management of data corrections via reconciliation requests from external client(s).
Confirm clinical datasets are prepared and transferred to the sponsor in compliance with applicable regulations.
Support peers in secondary document review and quality control activities for their assigned projects.
Transfer datasets utilizing acceptable data exchange locations, such as internal or external data portal locations.
Attend and/or host internal or external meetings as appropriate.
Manage complex workload from assigned study projects with priority clients and expedited timelines.
Mentor and train staff in support of business needs and team development.
Develop, implement, and maintain data templates, tools.
Draft and/or update relevant SOPs and other procedural documents.
Able to function as team lead and support the Supervisor as needed with scheduling and other administrative activities.
All other duties as assigned.

Skills and Experience:

Bachelor’s degree within Life Sciences essential.
Knowledge of CDISC’s CDASH, SDTM, and Controlled Terminology Standards.
Significant experience of working within a similar clinical data management role, in other CRO or Pharmaceutical environments.
Excellent communication skills and ability to work well with internal/external stakeholders
Familiarity with various data output formats (.xml, .xpt, sas7bdat, ASCII, text, .DAT, .xlsx).
Knowledge of Microsoft Office Suite and ability to perform basic computer functions commensurate with the job responsibilities.
Excellent organizational skills and the ability to meet deadlines.
Excellent communication (both written and verbal), leadership and negotiation skills.
Ability to interact appropriately with clients and all levels of employees, while at the same time support the efforts of departmental teams.

All applicants must have full and permanent Right to Work in the UK as we are unable to provide sponsorship for this role.

The salary for this role is up to £40,000/annum + bonus + benefits. Please note that the salary varies within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to fostering a sense of belonging and work daily in this direction.

Apply Now

Refine Your Search

clinical data manager jobs in scotland

Clinical Data Manager

Clinical Advisor - Assistant Manager, Wellness Advisory Team

Health Information Manager

Services & Delivery Manager

Healthcare Scientist Associate Practitioner - Laboratory Medicine

Clinical Project Manager x 2

Part-time Chief Executive Officer (CEO)

Operations Manager

Clinical Manager - Staff Bank

Data Manager – West of Scotland Safe Haven

Healthcare Development Manager

Territory Manager - Scotland

Medical Writer - Publications

Hub Manager (Edinburgh)

R & D Scientist (Haematology)

Senior HR Business Partner

Head of Programme – Psychology Specialist Practice

Project Financial Analyst 2

Suicide Prevention Officer

Medical Records Summariser/Workflow Administrator

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