Parexel's Regulatory Medical Writing Services works closely with our clients around the world to develop and launch new medicines and treatments that improve healthcare for millions of patients. We’re one of the largest providers of medical writing services worldwide, and have managed thousands of writing projects in more than 29 countries across North and South America, Europe, Asia, and Africa. As a result of continued customer satisfaction and business growth, this global team is expanding and offers many opportunities for career development.
In this role, you’ll prepare clinical documents for comprehensive clinical trials and programs. Using compliant Parexel and sponsor formats, styles and management systems, you’ll manage clinical document deliverables such as model informed consent forms, clinical study reports, pharmacovigilance documents and more. Our Medical Writers also participate in ongoing professional development programs to maintain current knowledge in the various areas.
- Full Time
- Travel: No
- Glassdoor Reviews and Company Rating
Check out the top traits we’re looking for and see if you have the right mix.
"I really enjoy learning about the vast areas of clinical writing. Everyone is very professional,Christine, Medical Writer II
knowledgeable, and it is easy to communicate with other staff."
"Parexel makes it easy to communicate and interact with each other, which allowsKristy, Associate Manager
me access to expertise and knowledge beyond my own."
We are one truly global team working together to propel each client´s journey ahead faster.
We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
Opportunity to learn and grow through a performance and development goal-setting program.
Love where you work, and work where you love.
Opportunity to work on a wide range of therapeutic areas, document types and clinical projects.
|Clinical Study Report Narratives|
Analytical and problem-solving skills
Excellent interpersonal skills
Excellent verbal / written communication skills
Excellent organizational and prioritization skills
Ability to work collaboratively and effectively in a team environment
Client focused approach to work
Ability to evaluate data and draw conclusions independently
A flexible attitude with respect to work assignments and new learning
Ability to negotiate on behalf of the department to ensure resources, timelines and expectations are aligned
Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
Fluency in written and spoken English
Computer proficiency, IT skills, the expertise and an ability to work with web-based applications, and familiarity with the Windows Operating system and the MS Office suite (Word/Excel/Power Point)
Gains trust and establish a connection with the client beyond one's project, to gain repeat business and/or to widen existing scope and services.
Provides departmental expertise and perspectives to promote prospective business opportunities.
Capability to make concise, accurate and relevant synopses of medical text and data, and the ability to write unambiguous medical text
Typing and transcription accuracy
Awareness of global culture
Knowledge and Experience:
Relevant experience is desirable in Regulatory/ Pharmacovigilance or related field.
Good knowledge of medical terminologies
Science/Medicine degree: The minimum qualification required would be a university degree in life Sciences/Health or Biomedical Sciences (Pharmacy, microbiology, Biochemistry, Biotechnology, Biophysics etc.)
A degree in Medicine/Dentistry/Physiotherapy/Experimental Medicine/Nursing, which involves patient exposure in hospital-based environment, would be an advantage
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