Clinical data manager Work, Jobs in Hook, Ham (with Salaries)

Senior Medical Writer
IQVIA —Reading
- Doctoral degree
- Computer literacy
- Master's degree
8d
Associate Clinical Project Manager (UK)
UCB —Slough
- Doctoral degree
- English
- Machine learning
15h
Addictions Therapy Lead
Priory —Woking
- £41,200 a year
- Full-time
- Supervising experience
- Care plans
- Leadership
- Free parking
- Annual leave
Quick apply
8d
Mammographer - Bank Shifts
Bupa —Reading
- £23 an hour
- Part-time
- Bachelor's degree
- Annual leave
- Gym membership
Quick apply
Registered Nurse BANK
Ashbourne Court Care Home —Andover
- £23.50 an hour
- Part-time
- Nursing
- Free parking
Quick apply
Care Coordinator
Winchester City Primary Care Network —Winchester
- £13.50 - £14.56 an hour
- Part-time
- Microsoft Office
- Administrative experience
- In-person
Quick apply
Medical Innovation Manager
Procter & Gamble —Reading
- £45,000 a year
- Full-time
- Doctoral degree
- English
- Employee stock ownership plan
Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea —Maidenhead
- Full-time
- Remote
- Presentation skills
- Mentoring
- Leadership
Pharmacovigilance Manager
Sanofi —Reading
- Full-time
- Hybrid work
- Management
- In-person
- Communication skills
SSCA Cancer Improvement Manager - Band 8a
Royal Surrey NHS Foundation Trust —Guildford
- £59,798 - £67,020 a year
- Full-time
- Analysis skills
- In-person
- Leadership
13d
Digital Learning and Skills Lead
HCRG Care Group —Guildford
- £46,000 a year
- Remote
- Data analysis skills
- Project management
- AI
- Employee discount
Quick apply
1d
Senior Physiotherapist
Circle Health Group —Basingstoke
- Up to £42,000 a year
- Full-time
- Patient care
- Organisational skills
- Leadership
- Employee discount
- Life insurance
11d
Global Data Manager - homebased (FSP)
IQVIA —Reading
- Remote
- Bachelor's degree
Patient Services Manager
Salus Medical Services —Farnborough
- £32,125 a year
- Part-time
- Customer service
- Administrative experience
- Mentoring
- Free parking
- Health & wellbeing programme
Quick apply
5d
Wider Workforce Lead
NHS England —Reading
- £57,528 - £64,750 a year
- Part-time
- Leadership
- Annual leave
Clinical Specialist, Advanced Access - South London
BD —Winnersh
- £43,300 - £66,025 a year
- Maintenance
- Supervising experience
- Mentoring
Professional Services Consultant - ICE
Clinisys —Woking
- Remote
- Customer service
- SQL
- Project management
13d
QA Senior Manager
Fortrea —Maidenhead
- Full-time
- Bachelor's degree
- Leadership
- Negotiation
Senior Clinical Programmer I
Allucent —Bracknell
- Full-time
- Hybrid work
- Computer Science
- Bachelor's degree
- Flexible schedule
- Referral programme
Quick apply
Chief Cardiac Physiologist (EP)
Ashford and St. Peter's Hospitals NHS Foundation Trust —Chertsey
- £51,657 - £58,785 a year
- Weekend availability
- Annual leave
- Employee discount

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clinical data manager jobs near hook, ham

Senior Medical Writer

IQVIA -
Reading

Apply Now

Job details

8 days ago

Qualifications

Doctoral degree
Computer literacy
Master's degree
Statistical analysis
Bachelor's degree
Technical writing
Medical terminology
Communication skills
Negotiation

Full job description

Job Overview
Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs Senior Review of straightforward medical writing deliverables. Negotiates timelines and discusses/resolves customer comments.
Provides written and verbal feedback to junior staff, and to customers when appropriate.
Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or technical writing.

Essential Functions

Take a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating and adhering to timelines, organizing document reviews, communicating directly with the customer.
Plan and organize workload for assigned projects and tasks: identify project needs, track timelines and implement customer requests.
Lead meetings on more challenging topics independently.
May present on standard Medical Writing processes at full-service bid defense meetings.
Assist in the training and development of junior staff, either formally as an assigned mentor or ad hoc for local colleagues or others. May develop and deliver training to the global team on a topic he/she has specific expertise in. May input into and deliver presentations on Medical Writing to other IQVIA groups.
May act as Project Manager for a more complex but single Medical Writing project which includes Project Finance/Invoicing responsibilities.
Complete project finance activities, including monitoring and forecasting budgeted hours.
Propose, review and approve budgets and costings for routine projects, including estimation of hours needed for Medical Writing tasks.
May take on a small customer lead role or assist an established partnership lead in their role.
May represent region or site on a Medical Writing initiative or cross-functional initiative.
Facilitates and brainstorms the identification of new ideas. May represent Medical Writing at a general capabilities audit.

Qualifications

Bachelor's Degree Bachelor's Degree in life sciences related discipline or related field
Master's Degree Master's Degree in life sciences related discipline or related field
Ph.D. Ph.D. in life sciences related discipline or related field
Typically requires at least 3 years of highly relevant experience and related competency levels.
In-depth knowledge of the structural and content requirements of clinical study reports, protocols, and similar documents and ability to identify deficiencies, errors, and inconsistencies in a protocol or report.
Good understanding of common statistical methods used in clinical trials and/or interpretation of their results.
Ability to effectively review a statistical analysis plan and to identify deficiencies, errors, and inconsistencies in statistical output
Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner.
Significant experience as a lead writer in preparing CSRs and protocols, with consistently positive feedback from customers and colleagues.
In depth knowledge of drug development, medical writing, and associated regulations. Good understanding of statistical principles and of medical terminology across a range of therapeutic areas.
Excellent written and oral communication skills including grammatical/technical writing skills.
Excellent attention to detail and accuracy.
Confident and effective communication and negotiation skills with customers and project managers.
Able to deliver difficult messages in constructive manner.
Demonstrates initiative and sound judgement when faced with less familiar project/document situations or challenges.
Demonstrated abilities in collaboration with others and independent thought.
Demonstrates confidence and maturity in most routine medical writing situations.
Demonstrates good judgement in requesting input from senior staff.
Ability to establish and maintain effective working relationships with coworkers, managers and customers.
Ability to effectively manage multiple tasks and projects.
Ability to proactively evaluate risks and potential issues and seek solutions and discuss appropriately with colleagues and customers.
Must be computer literate.

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

Refine Your Search

clinical data manager jobs in hook, ham

Senior Medical Writer

Associate Clinical Project Manager (UK)

Addictions Therapy Lead

Mammographer - Bank Shifts

Registered Nurse BANK

Care Coordinator

Medical Innovation Manager

Senior Clinical Data Manager - sponsor dedicated - oncology

Pharmacovigilance Manager

SSCA Cancer Improvement Manager - Band 8a

Digital Learning and Skills Lead

Senior Physiotherapist

Global Data Manager - homebased (FSP)

Patient Services Manager

Wider Workforce Lead

Clinical Specialist, Advanced Access - South London

Professional Services Consultant - ICE

QA Senior Manager

Senior Clinical Programmer I

Chief Cardiac Physiologist (EP)

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