Medical Writer Editor

Delta Pharma works with proven industry leaders who value character, integrity and professional growth.  We are committed to developing relationships that go beyond titles and reveal the core values desired by our clients in today’s highly competitive search for talent.  This successful approach is how the dedicated people of Delta Pharma match uncommon talent with extraordinary opportunities.

 

Actively participate in the production of periodic and ad hoc DS medical and regulatory reports including, but not limited to, safety sections of Clinical Study Reports and health authority submissions, periodic adverse event reports and issue work-ups. The activities include writing, editing and coordinating production for adverse event narratives and safety-related documents. Create and maintain departmental and safety-related document templates
* Participate in committees, departmental initiatives, clinical team filing activities,and special projects in collaboration with DS senior management. 

 

Excellent verbal and written communication skills, organizational skills and time and resources management skills. Able to partner effectively with internal and external partners in a proactive, positive and constructive manner. Able to manage multiple projects and timelines, and accommodate multiple priorities in a fast paced and changing environment. 

 

Bachelor’s degree in Science or Business-related field. Minimum 5 years of medical writing or equivalent experience Highly skilled in Microsoft Office applications, Adobe Acrobat, PowerPoint and other relevant applications for writing, editing, development of controlled documents etc. Knowledge of biotechnology/pharmaceutical industry, the clinical drug development process, and drug safety preferred. 

 

 

For Immediate Consideration contact Jennifer Marks

847-374-8250 x246

jmarks@delta-pharma.com