Medical Writer - Medical Information

Thermo Fisher Scientific • Wilmington, NC

1d • Onsite

About The Position

The Medical Writer will p r o v i d e h i g h - q u a l i t y m e d ic a l a n d s ci e n t i f ic w r i t i n g f r o m p l a nn i n g a n d c oo r d i n a t ion t h r ou g h d e l i v e r y o f f i n a l d r a f t s t o i n t e r n a l a n d e x t e r n a l cl i e n t s . C o l l a b o r a t e s w i t h i n t e r n a l a n d e x t e r n a l cl i e n t s , s u pp o r t i n g a n d e n a b l i n g e ff e c t i v e a n d e ff ic i e n t c o mm un i c a t ion t h a t r e s u l t s in o p e r a t i o n a l e x c e l l e n c e.

Requirements

• PharmD
• Experience with Medical Information (equivalent to 2+ years)
• P r e v io u s e x p e r i e n ce t h a t p r o v i d e s t h e k n o w l e dg e , s k i l l s a n d a b i l i t i e s t o p e r f o r m t h e j o b (co m p a r a b le t o 2 + y e a r s )
• S o l i d m e d ic a l wr i t i n g s k i l l s , i n cl ud i n g g r a m m a t ic a l, e d i t o r i a l a n d p r oo f r e a d i n g s k i l l s
• A b i l i t y t o i n t e r p r e t a n d p r e s e n t c o m p l e x d a t a a cc u r a t e ly a n d c o n ci s e ly
• E ff e c t i v e a d m i n i s t r a t i v e , o r g a n i z a t io n a l a n d p l a nn i n g s k i l l s ; a tt e n t ion t o d e t a il a n d q u a l i t y
• A b i l i t y t o w o r k o n o w n i n i t i a t i v e a n d e ff e c t i v e ly w i t h in a t e a m
• E ff e c t i v e o r a l a n d wr i t t e n c o mm un ic a t ion s k i l ls
• Gr e a t j u dg m e n t a n d d e ci s io n - m a k i n g s k i l ls
• G oo d c o m p u t e r s k i l ls a n d s k i l l e d w i t h cl i e n t t e m p l a t e s ; g oo d k n o w l e dg e o f d o c u m e n t m a n a g e m e n t s y s t e m s a n d o t h e r r e l e v a n t a pp l i c a t io n s ( e . g . E x c e l, O u t lo o k )
• Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
• Able to work upright and stationary for typical working hours.
• Ability to use and learn standard office equipment and technology with proficiency.
• Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

Nice To Haves

• E x p e r i e n ce working in the pharmaceutical / CRO industry preferred

Responsibilities

• Develops and updates standard medical response documents, custom response documents, frequently asked questions, and Academy of Managed Care Pharmacy formulary dossiers, specific to the peri- and post-approval phases of the product lifecycle.
• Researches and responds to escalated medical information inquiries from healthcare providers.
• Conducts literature searches for standard response documents utilizing secondary databases.
• Utilizing professional judgment, integrates pertinent clinical data into standard response documents with clear, concise, accurate and balanced medical writing following organizational, client, and regulatory guidelines.
• Participates as required in project launch meetings, review meetings, and project team meetings, serving as a liaison for communication with the client.
• Collaborates and effectively communicates with internal and external client contacts to provide high quality medical information writing deliverables in a timely manner and within budget.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree
• Number of Employees: 5,001-10,000 employees