ICON plc
Senior Clinical Trial Manager(m/w/x)
Full-timeRemoteSenior
Mannheim
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ICICON plc
Senior or Principal Medical Writer(m/w/x)
Mannheim
Full-timeRemoteSenior
Nejo AI Summary
Leading preparation and editing of clinical study documents for a global CRO. Advanced degree and strong understanding of regulatory requirements required. 4-day work week, company car for private use.
Requirements
- Advanced degree in Life Sciences, Pharmacy, Medicine, or related field
- Proficiency in interpreting and summarizing clinical trial data, research findings, and statistical analyses
- Excellent writing, editing, and proofreading skills
- Ability to communicate scientific concepts to diverse audiences
- Strong understanding of regulatory requirements (ICH-GCP, FDA, EMA)
- Experience interacting with regulatory agencies
- Ability to work effectively in fast-paced, deadline-driven environment
- Ability to manage multiple projects simultaneously
- Ability to prioritize tasks based on project timelines
- Excellent interpersonal and communication skills
- Ability to collaborate effectively with cross-functional teams
- Ability to build relationships with key stakeholders
- Ability to influence decision-making processes
- Encouraged to apply even if not meeting all requirements
Tasks
- Lead preparation, review, and editing of clinical study documents
- Ensure accuracy, clarity, and compliance with regulatory guidelines
- Collaborate with cross-functional teams to interpret clinical trial data
- Summarize scientific findings and communicate key insights
- Participate in planning and execution of clinical development programs
- Provide strategic input and scientific expertise
- Develop publication plans, abstracts, posters, and manuscripts
- Submit study results to peer-reviewed journals and scientific conferences
- Mentor and coach junior medical writers
- Provide guidance on best practices and scientific principles
- Foster a culture of excellence, collaboration, and continuous learning
Work Experience
- 4 - 7 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Additional Allowances
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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ICICON plc
Senior or Principal Medical Writer(m/w/x)
Mannheim
Full-timeRemoteSenior
Nejo AI Summary
Leading preparation and editing of clinical study documents for a global CRO. Advanced degree and strong understanding of regulatory requirements required. 4-day work week, company car for private use.
Requirements
- Advanced degree in Life Sciences, Pharmacy, Medicine, or related field
- Proficiency in interpreting and summarizing clinical trial data, research findings, and statistical analyses
- Excellent writing, editing, and proofreading skills
- Ability to communicate scientific concepts to diverse audiences
- Strong understanding of regulatory requirements (ICH-GCP, FDA, EMA)
- Experience interacting with regulatory agencies
- Ability to work effectively in fast-paced, deadline-driven environment
- Ability to manage multiple projects simultaneously
- Ability to prioritize tasks based on project timelines
- Excellent interpersonal and communication skills
- Ability to collaborate effectively with cross-functional teams
- Ability to build relationships with key stakeholders
- Ability to influence decision-making processes
- Encouraged to apply even if not meeting all requirements
Tasks
- Lead preparation, review, and editing of clinical study documents
- Ensure accuracy, clarity, and compliance with regulatory guidelines
- Collaborate with cross-functional teams to interpret clinical trial data
- Summarize scientific findings and communicate key insights
- Participate in planning and execution of clinical development programs
- Provide strategic input and scientific expertise
- Develop publication plans, abstracts, posters, and manuscripts
- Submit study results to peer-reviewed journals and scientific conferences
- Mentor and coach junior medical writers
- Provide guidance on best practices and scientific principles
- Foster a culture of excellence, collaboration, and continuous learning
Work Experience
- 4 - 7 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Additional Allowances
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
Not a perfect match?
- ICON plc
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