Senior Medical Writer
Posted on: January 16, 2022
At Parexel you'll team up with some of the best minds in the
industry to get new treatments to the patients who need them most.
Right now we are recruiting for Home Based Senior Medical Writers
and Principal Medical Writers.
Parexel is one of the largest providers of medical writing services
worldwide and has managed thousands of writing projects in more
than 29 countries in North and South America, Europe, Asia, and
Africa. As a result of continued customer satisfaction, the Team is
growing. We are currently looking for:
Home Based Clinical Regulatory Medical Writers in the US and Canada
(Full Time & Temporary Roles Available)
As a Parexel Medical Writer, you will be exposed to different
project teams, therapies and devices, as well as a diverse
portfolio of clients. The ability to understand our clients' needs
and achieve quality results is critical for us to continue to be
one of the best clinical research organizations (CROs) in the
world. To accomplish this, we believe that you must have the
ability to work independently as well as collaboratively every
As a Senior Medical Writer with Parexel you will research, create,
and edit all documents associated with clinical research.
Responsibilities include: lead author and primary client contact
for medical writing projects, working with other Parexel
departments and clients to set and meet internal/external
deliverable timelines, project leadership, and training and support
of junior medical writing staff.
Our writers are an integral part of clinical teams that support our
clients worldwide and they assist those teams in writing and
coordinating successful documentation across a wide range of
Use your clinical knowledge to write and edit clinical study
Use your project management skills to lead teams to quality and
Partner with sponsors as their primary client contact for medical
writing projects Mentor and train junior medical writing staff
Excellent interpersonal, verbal, and written communication
Consistently produces documents of high quality.
The ability to stay focused under tight timelines.
Attention to detail and proactivity.
Understands all necessary steps in a project, plan ahead, and
identify critical paths.
A flexible attitude with respect to work assignments and new
learning; readily adapts to changes.
Efficiently manages time spent on tasks and proactively identifies
deficiency. Manages multiple and varied tasks with enthusiasm and
prioritizes workload with attention to detail, e.g., organizational
Competent working in a matrix environment and values the importance
of teamwork. Possesses team leadership skills and cross-cultural
Negotiates on behalf of medical writing to ensure resources,
timelines and expectations are aligned.
Understands and satisfies client needs.
Gains trust and establishes a connection with the client beyond
one's project. Knowledge and Experience:
Demonstrated understanding of clinical research, the drug
development process, and industry guidelines and regulations, e.g.,
Accountable to provide document-specific advice to clients.
Scientific background essential.
Extensive clinical/scientific writing experience is required and
consists of multiple clinical documents: study reports, study
protocols, CTD documents and/or similar.
Advanced word processing skills, including MS Office (expertise in
Word); software and systems knowledge and ability to learn and
adapt to various IT systems: document management systems,
collaborative authoring (e.g., SharePoint), and file conversion and
Fluent in written and spoken English with appropriate attention to
phraseology, grammar, and punctuation. Education:
Bachelor's degree in Life Sciences/Health Related Sciences or
equivalent. Employment is contingent on disclosure of your COVID-19
vaccination status and, if relevant, proof of vaccination.
EEO Disclaimer Parexel is an equal opportunity employer. Qualified
applicants will receive consideration for employment without regard
to legally protected status, which in the US includes race, color,
religion, sex, sexual orientation, gender identity, national
origin, disability or protected veteran status.
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