Sr. Manager, Medical Writing
Alfasigma Group —Dublin, County Dublin
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
GMDP Quality Assurance Manager
WEP Clinical —Dublin, County Dublin
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Marketing Operations Manager
Photoroom —Dublin, County Dublin
- €60,000–€75,000 a year
- Full-time
- Remote
- SQL
- Analysis skills
- Marketing
- Annual leave
Industry Technical Consultant - PAC3 Micro-Electronics (GHT)
Ecolab —Dublin, County Dublin
- €63,200–€94,800 a year
- Engineering
- Bachelor's degree
- Leadership
15h
Global Clinical Project Manager - Vendor Management Expert (home-based in Europe)
IQVIA —Dublin, County Dublin
- Full-time
- Remote
- Project management
- Recruiting
- Communication skills
Head Groundsperson
Greyhound Racing Ireland —Dublin, County Dublin
- Full-time
- Continuous improvement
- Team management
- Leadership
Quick apply
14d
GCP Compliance Manager - Clinical Programs & Trials
Novartis —Dublin, County Dublin
- Full-time
- Engineering
- Communication skills
3d
Product Manager
Siena AI —Dublin, County Dublin
- Full-time
- Remote
- Master's degree
- AI
Internal Account Director (Recruitment & Retention)
サイネオス・ヘルス —Dublin, County Dublin
- €97,300–€170,300 a year
- Remote
- Microsoft Office
- Leadership
Clinical Data Management Lead, home-based
IQVIA —Dublin, County Dublin
- Full-time
- Remote
- Customer service
- Project management
- Bachelor's degree
Manager, Supply and Logistics
Tonix Pharmaceuticals Inc —Dublin, County Dublin
- Full-time
- Remote
- Microsoft Excel
- ERP systems
- Bachelor's degree
- Annual leave
- Employee assistance program
Quick apply
Clinical Engagement Project Manager
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Hotel
- Project management
- Presentation skills
- Gym membership
- Life insurance
Quick apply
Research Manager, Animal Health
Micron Agritech —Dublin, County Dublin
- Full-time
- Hybrid work
- Doctoral degree
- Research
- Master's degree
Grounds Maintenance & Racing Equipment Operator
Greyhound Racing Ireland —Dublin, County Dublin
- Full-time
- Maintenance
Quick apply
14d
Business Development Manager
Ecocem —Dublin, County Dublin
- Full-time
- Hybrid work
- Business development
- Construction
- Communication skills
Quick apply
Rapid Response
Kare Plan Ltd —South Dublin, County Dublin
- €33,000 a year
- 8 hour shift
- English
- No degree
- Patient care
- Employee assistance program
- Referral programme
Quick apply
2d
Clinical Trials Associate
Zymeworks Inc. —Swords, County Dublin
- €31,500–€48,300 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Office
- Bachelor's degree
- Annual leave
Quick apply
8d
Senior Clinical Editor
IQVIA —Dublin, County Dublin
- Full-time
- Doctoral degree
- English
- Research
Financial Reporting Manager
ARYZTA Ireland —Clondalkin, County Dublin
- Full-time
- Microsoft Excel
- Analysis skills
- Accounting
- Free parking
- Annual leave
Senior Enterprise Account Manager, AGS Ireland/NI (Cross Industries)
Amazon Web Services EMEA SARL (Irish Branch) —Dublin, County Dublin
- Full-time
- Sales
- AWS
- Negotiation
4d

I want to receive the latest job alerts for trial manager in dublin county dublin

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

trial manager jobs near dublin county dublin

Director Of Recruiting jobs in Dublin, County Dublin

Logistics Associate jobs in Dublin, County Dublin

Marketing Operations Manager jobs in Dublin, County Dublin

Clinical Data Manager jobs in Dublin, County Dublin

Research Manager jobs in Dublin, County Dublin

Quality Assurance Manager jobs in Dublin, County Dublin

Product Manager jobs in Dublin, County Dublin

Clinical Trial Manager jobs in Dublin, County Dublin

Director Of Learning Development jobs in Dublin, County Dublin

Global Tax Director jobs in Dublin, County Dublin

Director Of Nursing jobs in Naas, County Kildare

Healthcare Manager jobs in County Dublin

Regulatory Reporting jobs in Dublin, County Dublin

Operations Manager jobs in County Limerick

Financial Reporting Manager jobs in Dublin, County Dublin

Operations, Logistics, Warehouse, Supply Chain jobs in Carlow, County Carlow

Associate jobs in Letterkenny, County Donegal

Logistics Associate jobs in South Dublin, County Dublin

Operations Manager jobs in Dublin, County Dublin

Project Manager jobs in Limerick, County Limerick

Sr. Manager, Medical Writing

Alfasigma Group
Dublin, County Dublin

Apply Now

Job details

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Doctoral degree
Master's degree
Bachelor's degree

Full job description

Publish Date: May 20, 2026

GB Dublin

Sr. Manager, Medical Writing

Alfasigma is a privately held global healthcare company founded over 75 years ago in Italy, where it remains headquartered today in Bologna and Milan. The Group operates in over 100 markets spanning Europe, North and South America, Asia, and Africa.

Over three years ago, we embarked on a transformative journey to become a truly global innovative healthcare company with a leading focus on Gastrointestinal (GI) health. We have experienced remarkable growth, nearly doubled our revenues, expanding geographically, and integrating several key acquisitions. We have also evolved our portfolio, expanded into rare and specialty segments, and strengthened our pipeline and people's capabilities.

But our journey is far from complete! In fact, this is just the beginning of a bold new chapter in Alfasigma's history. We are committed to advancing innovation and leveraging our deep expertise to provide better health and a better quality of life for patients and consumers worldwide and expand our reach across diverse markets.

As we continue to grow, we are seeking a Sr. Manager, Medical Writing. This is a remote based position and can be in Europe or on the East Coast of the US.

Scope of the role:

The Senior Manager, Medical Writing, leads authoring of complex documents for one or more clinical development program.

Your key responsibilities:

Leadership

Train junior medical writers on best practices in medical writing and regulatory submission processes.
Help oversee vendor partnerships.

Writing

Lead author (including content planning, writing, and review) for clinical study protocols, clinical study reports (CSRs), investigator brochures, other study-level documentation required for clinical trials.
Author individual modules of IND/CTA, NDA, MAA requests for information and briefing documents. etc.) for regulatory agencies.
Review Summary of Clinical Efficacy (SCE) and Summary of Clinical Safety (SCS) statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency.

Quality Control

Coordinate for the quality and compliance of written components to company standards as well as regulatory requirements.

Project Management

Create document timelines and coordinate reviews with cross-functional teams and contract research organizations (CROs).
Manage vendor/contract medical writers

Collaboration

Collaborate with cross-functional teams to analyze complex scientific data for the above-mentioned document types.
Lead the document review process for study-level, submission, and regulatory interaction documents, through management of timelines, scheduling of meetings, and incorporation of feedback from cross-functional team
Represent Medical Writing on Clinical Study Team(s) (CST[s])

Literature Reviews

Conduct thorough literature reviews and synthesize complex scientific data into clear and concise documentation.

Department Administration

Oversee quality and adherence to document templates and standard operating procedures (SOPs)

Regulatory Standards

Ensure all documents adhere to regulatory guidelines, formatting standards, and internal quality standards.
Maintain up-to-date knowledge of industry trends and regulatory changes and provide oversight to ensure that standards are being applied through review of documents produced by other team members.

Who are you:

Work Experience / Education

Bachelor's degree in life sciences with minimum 8 years’ relevant experience in medical writing or pharmaceutical industry and/or clinical research OR
Advanced scientific degree (MS, PhD, Pharm D) with a strong background in relevant scientific discipline with minimum 5 years of relevant experience in medical writing or pharmaceutical industry and/or clinical research
Experience supporting and/or leading individual components of INDs, NDAs, and MAAs, as well as briefing books

Competencies & Major Skills

Strong verbal and written communications skills coupled with general knowledge of FDA and ICH rules, regulations and guidelines governing conduct of clinical studies and regulatory documents
Detail-oriented, with good organizational, prioritization, and time management proficiencies; proactive approach.
Ability to work cross-functionally
Advanced computer software experience (including but not limited to MS Word, Excel, PowerPoint)
Ability to interpret and present scientific and clinical trial data and understand statistical methods and analysis plans.
Proven ability to facilitate issue/comment resolution as it relates to finalization of medical writing deliverables.

Ability to thrive and adapt in times of uncertainty

Why Join Alfasigma:

At Alfasigma, we foster a culture where the courage to innovate is key to our success.
We offer a competitive salary, comprehensive benefits, and extensive opportunities for professional growth and development.

Our commitment to people and patients is at the heart of everything we do. We value diversity and welcome individuals with unique perspectives and experiences. We believe that open-mindedness, collaboration, and a shared passion for innovation are essential to achieving meaningful progress.

Join Alfasigma and become part of a forward-thinking team dedicated to shaping the future of the pharmaceutical industry.

Alfasigma is committed to a policy of Equal Employment Opportunity and will not discriminate against an applicant or employee on the basis of race, religious creed, religious observance, color, age, sex, sexual orientation, gender, gender identity, gender expression, genetic information, national origin, ancestry, marital status, medical condition as defined by state law (cancer and genetic characteristics), disability, military service, military and veteran status, pregnancy, childbirth and related medical conditions, or any other classification protected by federal, state, and local laws and ordinances. Applicants with disabilities may be entitled to reasonable accommodation under the terms of the Americans with Disabilities Act and certain state or local laws. A reasonable accommodation is a change in the way things are normally done which will ensure an equal employment opportunity without imposing undue hardship on the Company. Please email Human Resources at [email protected] if you need assistance completing any forms or to otherwise participate in the application process.

Apply Now

Refine Your Search

trial manager jobs in dublin county dublin

Sr. Manager, Medical Writing

GMDP Quality Assurance Manager

Marketing Operations Manager

Industry Technical Consultant - PAC3 Micro-Electronics (GHT)

Global Clinical Project Manager - Vendor Management Expert (home-based in Europe)

Head Groundsperson

GCP Compliance Manager - Clinical Programs & Trials

Product Manager

Internal Account Director (Recruitment & Retention)

Clinical Data Management Lead, home-based

Manager, Supply and Logistics

Clinical Engagement Project Manager

Research Manager, Animal Health

Grounds Maintenance & Racing Equipment Operator

Business Development Manager

Rapid Response

Clinical Trials Associate

Senior Clinical Editor

Financial Reporting Manager

Senior Enterprise Account Manager, AGS Ireland/NI (Cross Industries)

I want to receive the latest job alerts for trial manager in dublin county dublin

Related Searches

Explore jobs in more locations

Sr. Manager, Medical Writing

Jobseeker tools

Employer Tools

Browse

Stay Connected