drjobs Senior Medical Writer - Remote English

Senior Medical Writer - Remote

صاحب العمل نشط

drjobs

حالة تأهب وظيفة

سيتم تحديثك بأحدث تنبيهات الوظائف عبر البريد الإلكتروني
Valid email field required
أرسل الوظائف
drjobs
أرسل لي وظائف مشابهة
drjobs

حالة تأهب وظيفة

سيتم تحديثك بأحدث تنبيهات الوظائف عبر البريد الإلكتروني

Valid email field required
أرسل الوظائف
موقع الوظيفة drjobs

Pune - الهند

الراتب الشهري drjobs

لم يكشف

drjobs

لم يتم الكشف عن الراتب

الوصف الوظيفي

Responsibilities:

  • Produce wellwritten highquality timely Medical Writing documents (like Clinical Study Reports Protocols and amendments Investigators Brochure IB and IB updates etc)
  • Review (including peer and QC review) Medical Writing documents in accordance with current SOPs ensuring checklists and tracking documents are completed
  • Proofread and provide editorial support on documents produced by other departments in company or by clients if requested
  • Provide oversight on Medical Writing projects and/or crossfunctional projects using project management tools and processes
  • Manage the document review process ensuring conflicting and/or ambiguous comments are clarified and adequately addressed
  • Assist Principal Medical Writers and above with the management of department budget and financials
  • Actively contribute to business development by keeping CV uptodate preparing and reviewing client proposals and other business development documentation as well as presenting at client meetings and bid defense meetings
  • Line manage assigned personnel taking an active role in their development and provide guidance and mentorship to less experienced Medical Writers
  • Conduct literature reviews and provide input on the development of scientific communication and messaging
  • Manage timelines and deliver documents within established deadlines

Requirements

  • Masters degree or higher in a life science or related field.
  • Minimum 5 years of experience as a Medical Writer in the pharmaceutical biotechnology or CRO industry.
  • Strong knowledge of clinical research regulatory requirements and industry guidelines (ICHGCP).
  • Excellent writing editing and proofreading skills with the ability to communicate complex scientific information effectively.
  • Experience in writing clinical study documents such as protocols clinical study reports and regulatory submission documents.
  • Detailoriented with excellent organizational and time management skills.
  • Ability to work independently and collaboratively in a team environment.

Lifelancer ( ) is a talenthiring platform in Life Sciences Pharma and IT. The platform connects talent with opportunities in pharma biotech health sciences healthtech data science and IT domains.

Please use the below Lifelancer link for job application and quicker response.

/jobs/view/8e908a8f93f58bd9d74aa2d21cc363de

Remote Work :

No

نوع التوظيف

دوام كامل

نبذة عن الشركة

الإبلاغ عن هذه الوظيفة
إخلاء المسؤولية: د.جوب هو مجرد منصة تربط بين الباحثين عن عمل وأصحاب العمل. ننصح المتقدمين بإجراء بحث مستقل خاص بهم في أوراق اعتماد صاحب العمل المحتمل. نحن نحرص على ألا يتم طلب أي مدفوعات مالية من قبل عملائنا، وبالتالي فإننا ننصح بعدم مشاركة أي معلومات شخصية أو متعلقة بالحسابات المصرفية مع أي طرف ثالث. إذا كنت تشك في وقوع أي احتيال أو سوء تصرف، فيرجى التواصل معنا من خلال تعبئة النموذج الموجود على الصفحة اتصل بنا