8 beste vacatures voor de functie van content manager in 2151 nieuw vennep (nieuwe medewerkers gezocht)

Senior Medical Writer
IQVIA —Amsterdam
- Fulltime
- Doctor
- Schrijfvaardigheden
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iO —Amsterdam
- Fulltime
- Hybride werken
- Engels
- Bachelor
- AI
- Budget voor professionele ontwikkeling
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Junior Content Creative (Dutch Speaking)
Gran Julia Socials —Amsterdam
- € 2.500 - € 3.700 per maand
- E-mail
- Socialemediabeheer
- Tijdmanagement
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2 dagen
Marketing & Communicatie stage
WPP Media —Amsterdam
- € 450 per maand
- Marketing
- Stage
- Communicatieve vaardigheden
7 dagen
Meewerkstage Digitale Content
de Bijenkorf —Amsterdam
- € 250 - € 350 per maand
- Parttime
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Content Marketing Stagiair
Triple Solar —Amsterdam Noord
- E-mail
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Stage Content Marketing
Brandfirm —Amsterdam
- € 500 per maand
- Fulltime
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- Tijdmanagement
Marketing Communicatie Stagiair(e) – HQ Haarlem
Pepperminds —Haarlem
- € 300 per maand
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Senior Medical Writer

IQVIA -
Amsterdam

Nu solliciteren

Vacaturegegevens

Fulltime

Kwalificaties

Doctor
Schrijfvaardigheden
Master
Bachelor
Klinische studies
Medische terminologie
Communicatieve vaardigheden
Onderhandelen

Volledige vacaturetekst

Amsterdam, Netherlands | Full time | Home-based | R1554306

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.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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content manager vacatures in 2151 nieuw vennep

Senior Medical Writer

Contentmanager

Junior Content Creative (Dutch Speaking)

Marketing & Communicatie stage

Meewerkstage Digitale Content

Content Marketing Stagiair

Stage Content Marketing

Marketing Communicatie Stagiair(e) – HQ Haarlem

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Ik wil de nieuwste vacature-alerts ontvangen voor de functie van content manager in 2151 nieuw vennep

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