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
- Level: Mid
- Travel: No

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- Detail-Oriented
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Rewards
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Global Impact
We are one truly global team working together to propel each client´s journey ahead faster.
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Work-life Balance
We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
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Career Development
Opportunity to learn and grow through a performance and development goal-setting program.
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Home based
Love where you work, and work where you love.
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Variety
Opportunity to work on a wide range of therapeutic areas, document types and clinical projects.
Responsibilities
Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. We believe in our values, Patients First, Quality, Respect, Empowerment & Accountability.
Parexel are recruiting for a Senior Medical Writing Support Coordinator (MWSC) within our Functional Service Provider (FSP) group. The FSP team is an outsourcing model that fulfills key clinical development roles across a variety of functional disciplines including medical writing.
As the Senior Medical Writing Support Coordinator (MWSC) you will provide support to Lead Medical Writers (LMWs) and management on Medical Writing Services (MWS) projects as appropriate, including administrative, filing and some document development support, if needed.
The role can be based in either Ireland, UK or South Africa and can be fully home based. You will be working in an innovative and collaborative environment with international peers, colleagues and a supportive manager.
Key Accountabilities:
Project Filing
Organize and track delivery of all project documents as required.
Project Related Support
Assist Medical Writers in all billable project-related tasks, as required.
This includes assisting with client communication, set up and maintenance of project files and archiving
General Administrative Support
Provide administrative support, including coordination of meetings, recording and distribution of meeting minutes, photocopying, faxing, and maintenance of project trackers, as required
Chase up with document reviewers if appropriate
Liaise with the MWS Head of Finance and Lead MW to communicate timelines for financial forecasting.
Liaise with assigned Document Specialist to organize source documents for appendices
Training MWs in new client procedures
Document Development Support
Optional, for certain partnerships:
Prepare QC source doc packages or SharePoint folder and schedule QC reviews.
Support MWs during document submission, including document development support and inspection readiness.
Education:
Not specified but a primary degree, especially in biological sciences or health-related sciences, along with good computational skills preferred.
Skills:
Conscientious, able to work with minimal supervision and accept work direction from Lead Medical Writers and MWS management.
Aptitude for working with a variety of different software packages.
Ability to handle matters of a confidential nature.
Excellent interpersonal, verbal and written communication skills.
Client-focused approach to work.
A flexible attitude with respect to work assignments and new learning.
Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.
Willingness to work in a matrix environment and to value the importance of teamwork.
Knowledge and Experience:
Previous Medial Writing administration or coordination experience desirable.
Knowledge of MS word processing, spreadsheet, database and e-mail applications desirable.
Basic knowledge of general administration or office practice.
In return we will be able to offer you a structured career pathway and encouragement to develop within the role including awareness and understanding of the industry. You will be well supported and in return for your hard work you will be rewarded with a competitive base salary and a benefits package including holiday, private healthcare as well as other benefits that you would expect with a top company in the CRO Industry.
Apply today to begin your Parexel journey!
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