Expert Writer
AI Summary
Expert Writer at Galderma prepares complex manuscripts, abstracts, posters, and slide sets from clinical data, performs quality control, manages multiple brands, and trains colleagues while maintaining compliance and project records.
About this role
With a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the leading company solely dedicated to skin and advancing the future of dermatology.
We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients and the healthcare professionals we serve every day. We aim to empower each employee and to promote their personal growth all the while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy and personal rights of every employee.
At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create unparalleled, direct impact.
Job Description
Responsibilities:
- Prepares, literature review, abstracts, posters, and slide sets, and Manuscripts (complex) working from various data sources including clinical study reports, patient profiles, protocols etc.
- Performs quality control (QC) checking / proof reading of the above mentioned deliverables to meet customer expectations.
- Manages multiple projects of up to two brands at any given time. Obtains feedback from customers and implements customer management tactics.
- Complies with and support group’s project management tool, standards, policies and initiatives.
- Follows Galderma specifications for documentation, styles, templates etc. Follows and tracks clinical trial milestones for assigned projects.
- Maintains records for all assigned projects including archiving. Maintains audit, SOP and training compliance.
- Trains new joiners, fellow colleagues as and when required. Performs additional tasks as assigned.
Minimum requirements
- Minimum science degree or equivalent, B.Sc./equivalent with 10 years Clinical Research (CR) experience, M.Sc./M.Pharma +8 years of clinical research (CR)
- Excellent written and oral English Minimum: Minimum science degree or equivalent, B.Sc./equivalent with 10 years Clinical Research (CR) experience, M.Sc./M.Pharma +8 years of clinical research (CR) experience Desired
- Doctoral Degree or Qualification in Medical Sciences (MBBS/MD/equivalent) PhD + 6 year of CR experience, MBBS/equivalent + 6 year of CR
Skills
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