Pharmaceutical consultant Work, Jobs in United Kingdom (with Salaries)

Regulatory Consultant - CMC (CMC with small molecule products)
サイネオス・ヘルス —Remote
- Remote
- Bachelor's degree
- Contracts
Real World Evidence (Associate Consultant)
Lane Clark & Peacock —London
- Hybrid work
- Microsoft Powerpoint
- Microsoft Outlook
- Doctoral degree
- Annual leave
- Employee discount
10d
Regulatory Affairs Consultant - CMC vax/bio (home or office based)
Parexel —Remote
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Consultant/Senior Consultant Life Sciences & Healthcare Strategy, Strategy & Business Design
Deloitte —London
- Hybrid work
- Business development
- Analysis skills
- Bachelor's degree
12d
Life Sciences Consultant, Management Consulting
Carnall Farrar —London
- Full-time
- Hybrid work
- Data analysis skills
- SQL
- Project management
- Work from home
- Employee assistance programme
Quick apply
7d
Associate Consultant (UK) - Entry-Level Technology Consulting (Life Sciences)
Veeva Systems —London
- £40,000 a year
- Full-time
- Hybrid work
- English
- Travel
- Communication skills
Associate Technical Consultant (UK) - Entry-Level Consulting (Life Sciences)
Veeva Systems —London
- £40,000 a year
- Full-time
- Hybrid work
- Azure
- Computer Science
- Java
Proposal Writer
Clinilabs, Inc —Remote
- £52,176 - £67,084 a year
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
7d
Senior Consultant to Senior Manager - Life Sciences Consulting
Simon-Kucher & Partners —London
- Analysis skills
- Work from home
Regulatory Affairs Consultant - Labelling Strategy (home or office based)
Parexel —Remote
- Remote
- English
- Bachelor's degree
- Communication skills
Consultant, Advanced Analytics: Meta-Analysis (HTA Statistician)
Parexel —Remote
- Remote
- Doctoral degree
- English
- Master's degree
Associate Consultant, Commercial Consulting
Clarivate —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Outlook
- Annual leave
- Gym membership
4d
Long Term Care Assoc Acct Mgr - Birmingham, AL
Teva —Birmingham
- £88,000 - £160,000 a year
- Nursing home
- Sales
- Bachelor's degree
- Annual leave
Medical Device Regulatory and Quality Consultant
PA Consulting —Melbourn
- Full-time
- Annual leave
Associate Consultant – Financial Institutions Consulting - Europe
IQVIA —London
- Full-time
- Hybrid work
- Doctoral degree
- English
- Master's degree
Pharma Quality Specialist Consultant
PA Consulting —London
- Full-time
- Hybrid work
- Communication skills
- Annual leave
Quick apply
Senior Regulatory Affairs Consultant - Labelling Strategy (home or office based)
Parexel —Remote
- Remote
- English
- Bachelor's degree
- Communication skills
Consultant (Clinical Outcome Assessment - COA)
Clarivate —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Outlook
- Doctoral degree
- Annual leave
- Gym membership
Consultant Market Access
IGES GmbH —London
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Life insurance
Quick apply
5d
Health Economics & Modelling Lead (Principal Consultant)
Parexel —Remote
- Remote
- Doctoral degree
- English
- Master's degree

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pharmaceutical consultant jobs near united kingdom

Regulatory Consultant - CMC (CMC with small molecule products)

サイネオス・ヘルス
Remote

Apply Now

Job details

Qualifications

Biology
Bachelor's degree
Contracts

Full job description

Updated: Today
Location: Remote, LND, United Kingdom
Job ID: 25108623

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Description

Regulatory Consultant - CMC (CMC with small molecule products)

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

Why Syneos Health

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

General Position Summary

The Chemistry Manufacturing Control Consultant will support the execution of multi-product global regulatory CMC for marketed products for small molecule products. Biologics / Cell and Gene Therapy experience. This role contributes to the preparation and submission of regulatory CMC documentation and provides regulatory support to various cross functional teams.

Key Duties and Responsibilities

Execute commercial Lifecycle Management (LCM) strategy and submissions with a focus on Middle East and North Africa or LATAM
Reviews CMC sections of regulatory submissions, as well as the interactions and responses with regulatory agencies for small molecule products
Works with regulatory colleagues in development of global regulatory CMC strategies and Submissions
Participates effectively on cross-functional teams and may serve as the primary regulatory CMC contact for assigned products and projects

Required Education Level & Experience

Bachelor's degree, with a preference in Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs, Biologics or Medical Devices, or another related life-science field
Typically requires 4 years of experience in the pharmaceutical industry or related field, or the equivalent combination of education and experience
Preferred experience supporting Small Molecule programs

Required Knowledge/Skills

Strong interpersonal skills to exchange complex information with others and to guide others
Ability to collaborate and communicate in an open, clear, complete, timely and consistent manner
Strong sense of planning and prioritization, and the ability to work with all levels of management

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Apply Now

Refine Your Search

pharmaceutical consultant jobs in united kingdom

Regulatory Consultant - CMC (CMC with small molecule products)

Real World Evidence (Associate Consultant)

Regulatory Affairs Consultant - CMC vax/bio (home or office based)

Consultant/Senior Consultant Life Sciences & Healthcare Strategy, Strategy & Business Design

Life Sciences Consultant, Management Consulting

Associate Consultant (UK) - Entry-Level Technology Consulting (Life Sciences)

Associate Technical Consultant (UK) - Entry-Level Consulting (Life Sciences)

Proposal Writer

Senior Consultant to Senior Manager - Life Sciences Consulting

Regulatory Affairs Consultant - Labelling Strategy (home or office based)

Consultant, Advanced Analytics: Meta-Analysis (HTA Statistician)

Associate Consultant, Commercial Consulting

Long Term Care Assoc Acct Mgr - Birmingham, AL

Medical Device Regulatory and Quality Consultant

Associate Consultant – Financial Institutions Consulting - Europe

Pharma Quality Specialist Consultant

Senior Regulatory Affairs Consultant - Labelling Strategy (home or office based)

Consultant (Clinical Outcome Assessment - COA)

Consultant Market Access

Health Economics & Modelling Lead (Principal Consultant)

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