20 beste Stellen als medical science in mannheim – aktuell auf Personalsuche

Senior OR Principal Medical Writer
ICON Plc —Mannheim
- Vollzeit
- Schreibfähigkeiten
- Forschungserfahrung
- Mitgliedschaft im Fitnessstudio
Regionalleiter m/w/d Nephrologie/Rare Diseases
IQVIA —Mannheim
- Vollzeit
- CRM-Software
- Englisch
- Analysefähigkeit
Site Activation Specialist - Germany
IQVIA —Mannheim
- Vollzeit
- Bachelor
5 Tage
Quality Engineer - MedTech (m/w/d) TZ/VZ
BD —Heidelberg
- 53.200 € – 81.100 € pro Jahr
- Teilzeit
- Englisch
- Microsoft Office
- Organisationstalent
Research Scientist – Proteomics Workflow Innovation (m/f/d)
GlaxoSmithKline —Heidelberg
- 55.050 € – 91.750 € pro Jahr
- Vollzeit
- Doktorat
- Datenanalyse
- Forschungserfahrung
7 Tage
Research assistant (f/m/d)
Universitätsklinikum Heidelberg —Heidelberg
- Teilzeit
- Kommunikationsfähigkeit
Intern (m/f/d) Clinical Trial Services
Phoenix Medical —Mannheim
- 2.322 € pro Monat
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible Arbeitszeiten
IT (Senior) Consultant für Regulatory Affairs, Medical Affairs oder Drug Safety - Life Science (w|m|d)
BridgingIT GmbH —Mannheim
- 65.000 € – 80.000 € pro Jahr
- Vollzeit
- Projektmanagement
- Erfahrung in der IT
- Weiterbildungsprogramme
- Flexible Arbeitszeiten
Direkt bewerben
Laboratory Scientist - Automation (Proteomics) (m/f/d)
GlaxoSmithKline —Heidelberg
- 55.050 € – 91.750 € pro Jahr
- Vollzeit
- Forschungserfahrung
- Master
- Python
7 Tage
Scientific Researcher (m/f/d)
Universitätsklinikum Heidelberg —Heidelberg
- Vollzeit
- Doktorat
- Englisch
- Machine Learning
- Flexible Arbeitszeiten
13 Tage
Prozessingenieur (m/w/d) Medizintechnik
BD —Heidelberg
- 65.000 € – 99.125 € pro Jahr
- Englisch
- Master
- Bachelor
7 Tage
Occupational Health Physican (f/m/d) - fixed-term two years
Freudenberg Service KG —Weinheim
Senior Scientist II (all genders) for Extractables and Leachables - PDS&T - Global Material and Parenteral Packaging Sciences - permanent fulltime
AbbVie —Ludwigshafen am Rhein
- Vollzeit
- Doktorat
- Master
- Bachelor
R&D Technician / Laborhilfe Development (all genders) - temporary 2 years
Reckitt —Heidelberg
- Employee Assistance Program
- Lebensversicherung
Intern (f/m/d) in the field Corporate Strategic Planning and Business Development / Mergers & Acquisitions, October 2026 - Duration: 2-3 Months
Freudenberg & Co. Kommanditgesellschaft —Weinheim
- Englisch
- Microsoft Office
- Wirtschaft
Risk Management System (RMS) & Internal Control System (ICS) Specialist (m/f/d)
BASF Agricultural Solutions Deutschland GmbH —Limburgerhof
- Künstliche Intelligenz
Postdoc - Deciphering resistance against targeted treatments in glioblastoma (m/w/d)
Universitätsklinikum Heidelberg —Heidelberg
- Vollzeit
- Doktorat
- Krankenhaus
- Künstliche Intelligenz
Data Analyst (m/f/d) Trading Analytics
Phoenix Medical —Mannheim
- Microsoft Excel
- Master
- SQL
Field Clinical Specialist Central Lower Saxony - Nurse Biomedical APM
BD —Heidelberg
- 52.100 € – 79.475 € pro Jahr
- Teilzeit
- Microsoft Office
- Präsentationserfahrung
- Künstliche Intelligenz
Operator 2 Molding
BD —Heidelberg
- 65.000 € – 99.125 € pro Jahr
- Englisch
- Master
- Bachelor
5 Std.

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Senior OR Principal Medical Writer

ICON Plc -
Mannheim

Jetzt bewerben

Details zur Stelle

Vollzeit

Leistungen

Mitgliedschaft im Fitnessstudio

Qualifikationen

Schreibfähigkeiten
Forschungserfahrung
Pharmazie

Vollständige Stellenbeschreibung

Senior or Principal Medical Writer

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

We are currently seeking a Senior or Principal Medical Writer to join our diverse and dynamic team. As a Senior Medical Writer at ICON, you will play a pivotal role in leading the development and execution of medical writing strategies for clinical research projects, contributing to the advancement of inNvative treatments and therapies.

What you will be doing

Leading the preparation, review, and editing of clinical study documents, including clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and regulatory submissions, ensuring accuracy, clarity, and compliance with regulatory guidelines and industry standards.
Collaborating closely with cross-functional teams, including clinical research, biostatistics, regulatory affairs, and medical affairs, to interpret and analyze clinical trial data, summarize scientific findings, and communicate key insights in written form.
Participating in the planning and execution of clinical development programs, providing strategic input and scientific expertise to support the design, conduct, and interpretation of clinical studies and research initiatives.
Contributing to the development of publication plans, abstracts, posters, and manuscripts for submission to peer-reviewed journals and presentation at scientific conferences, disseminating study results and scientific insights to the broader scientific community.
Mentoring and coaching junior medical writers, providing guidance on best practices, writing techniques, and scientific principles, and fostering a culture of excellence, collaboration, and continuous learning within the medical writing team.

Your profile

Advanced degree in Life Sciences, Pharmacy, Medicine, or related field, with a minimum of 4-7 years of experience in medical writing within the pharmaceutical, biotechnology, or contract research organization (CRO) industry.
Proficiency in interpreting and summarizing complex clinical trial data, scientific research findings, and statistical analyses, with excellent writing, editing, and proofreading skills, and the ability to communicate scientific concepts to diverse audiences.
Strong understanding of regulatory requirements (e.g., ICH-GCP, FDA, EMA) governing the preparation and submission of clinical documents and publications, and experience in interacting with regulatory agencies during the review and approval process.
Demonstrated ability to work effectively in a fast-paced, deadline-driven environment, managing multiple projects simultaneously and prioritizing tasks based on project timelines and deliverables.
Excellent interpersonal and communication skills, with the ability to collaborate effectively with cross-functional teams, build relationships with key stakeholders, and influence decision-making processes.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Jetzt bewerben

Erweiterte Suche

medical science Jobs in mannheim

Senior OR Principal Medical Writer

Regionalleiter m/w/d Nephrologie/Rare Diseases

Site Activation Specialist - Germany

Quality Engineer - MedTech (m/w/d) TZ/VZ

Research Scientist – Proteomics Workflow Innovation (m/f/d)

Research assistant (f/m/d)

Intern (m/f/d) Clinical Trial Services

IT (Senior) Consultant für Regulatory Affairs, Medical Affairs oder Drug Safety - Life Science (w|m|d)

Laboratory Scientist - Automation (Proteomics) (m/f/d)

Scientific Researcher (m/f/d)

Prozessingenieur (m/w/d) Medizintechnik

Occupational Health Physican (f/m/d) - fixed-term two years

Senior Scientist II (all genders) for Extractables and Leachables - PDS&T - Global Material and Parenteral Packaging Sciences - permanent fulltime

R&D Technician / Laborhilfe Development (all genders) - temporary 2 years

Intern (f/m/d) in the field Corporate Strategic Planning and Business Development / Mergers & Acquisitions, October 2026 - Duration: 2-3 Months

Risk Management System (RMS) & Internal Control System (ICS) Specialist (m/f/d)

Postdoc - Deciphering resistance against targeted treatments in glioblastoma (m/w/d)

Data Analyst (m/f/d) Trading Analytics

Field Clinical Specialist Central Lower Saxony - Nurse Biomedical APM

Operator 2 Molding

Ich möchte aktuelle Job-E-Mails für Stellen als medical science in mannheim erhalten

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