Head of Medical Writing Ophthalmology
(f/m/d)
Join our team and make a difference in the world of ophthalmology!
targomed has been a trusted partner in the field of medical writing and clinical studies for over a decade. We are now seeking a passionate and experienced Head of Medical Writing Ophthalmology (f/m/d) to join our team.
Your Responsibilities:
* Lead, coordinate and develop the Medical Writing Team
* Manage, supervise and coordinate scientific and regulatory medical writing projects in the field of medical devices in ophthalmology
* Prepare and review articles with predominantly medical content for publication in English (peer-review and trade journals)
* Create and review regulatory documents under the scope of EU MDR 2017/745 (e.g. Clinical Investigation Reports, Clinical Evaluation Reports, Clinical Evaluation Plans, PMCF Plans, SSCP,PSUR, etc.)
* Ensure the highest quality and scientific accuracy in all medical writing deliverables.
* Collaborate with interdisciplinary teams to ensure the quality and consistency of medical content
* Support data analysis in collaboration with Data Manager and Biostatistician.
* Assess and interpret clinical outcomes in Ophthalmology.
* Maintain a strong understanding of Good Clinical Practice and relevant regulatory guidelines.
Your Qualifications:
* Educational Background: Degree in medicine, natural sciences, or a related field with a focus on ophthalmology.
* Experience: Proven experience in scientific and regulatory medical writing within the ophthalmology field. At least 6 years of experience in Medical Writing, preferably in
Ophthalmology
* Experience in team and project leadership
* Excellent written and verbal communication skills
* Knowledge of regulatory requirements and guidelines (e.g., ICH-GCP)
* Ability to collaborate in an interdisciplinary team
* Soft Skills: Motivated, open-minded, communicative, and committed to delivering high-quality work.
* Organizational Skills: Ability to manage multiple projects simultaneously and prioritize tasks effectively.
* Regulatory Knowledge: Deep understanding of Medical Device Regulations (EU MDR 2017/745), especially in relation to the evaluation and reporting of clinical data.
* Language Skills: Excellent written and spoken English is essential; German is a plus.
What We offer:
* Diverse and Stimulating Environment: Work in a dynamic and collaborative team.
* Flexible Work Arrangements: Enjoy flexible working hours and the option to work remote.
* Supportive Culture: Benefit from a supportive and team-oriented work environment.
* Professional Growth: Opportunities to implement ideas and contribute to the team’s success.
* Open and Appreciative Collaboration: We value open communication and recognize the contributions of our team members.
* Full-Time or Part-Time Options (min. 30h): Choose the employment arrangement that best suits your needs.
Join our team and make a meaningful impact in the world of ophthalmology!
Please send your detailed application, including your expected salary, to jobs@targomed.de
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