At a Glance
- Tasks: Create impactful clinical study documents to support innovative medical solutions.
- Company: Join Convatec, a global leader in medical products and technologies.
- Benefits: Enjoy remote work flexibility, competitive salary, and opportunities for professional growth.
- Other info: Limited travel required, with excellent career advancement opportunities.
- Why this job: Make a real difference in patient lives while advancing your career in a dynamic environment.
- Qualifications: 7-10 years of experience in medical writing or relevant qualifications.
The predicted salary is between 56700 - 69300 £ per year.
Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With over 10,000 colleagues, we provide products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention, treatment for hard to heal wounds, at-risk skin and ulcerated tissue to supporting debilitating conditions, improved patient outcomes and reduced care costs.
Job Summary
Working within the Medical and Clinical Affairs organization, the Senior Medical Writer will be primarily responsible for the preparation of clinical study documents to support Convatec products in a range of pre- to post-market studies across global geographies. The successful Senior Medical Writer will engage cross-functional teams in the creation of these clinical study documents, ensuring best-fit study deliverables in support of Convatec products and the patients we serve.
Duties and Responsibilities
- Develop protocols, study reports, and additional clinical investigation materials to support clinical study programs across Convatec Business Units
- Prepare data summaries for internal audiences as well as external HCPs, patients, and regulatory authorities
- Implement Good Clinical Practice in the development of all clinical study documents
- Perform literature searches and reviews to support clinical study design, strategic decision making, novel methods
- Stay current on registered studies and published literature within relevant therapy spaces and advise internal teams accordingly
Travel Requirements
This is a remote role with limited travel requirements. Travel within country may include quarterly team meetings at Convatec facilities and/or relevant scientific conferences. This role may involve limited international travel, maximum twice per year.
About You
- BSc + 7–10 years’ relevant experience OR MSc + 3–5 years’ relevant experience OR PhD or equivalent in an appropriate subject
- Experience in writing clinical study documents
- Trained in Good Clinical Practice
- Knowledge of CTMS and eTMF preferred
- Knowledge of medical device/pharmaceutical industry preferred
- Excellent written communication skills
- Good working knowledge of Embase and PubMed
Our progress will give you countless opportunities to move forward too. Seek out new challenges, and you’ll find them. Stretch your thinking, and you’ll find new ways to make an impact. And if you embrace the opportunity to drive your own growth, you could go further, and achieve more, than ever before.
Equal opportunities
Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.
Senior Medical Writer - Clinical Operations employer: ConvaTec
At Convatec, we pride ourselves on being an exceptional employer, offering a collaborative and innovative work culture that empowers our employees to thrive. As a Senior Project Manager, you will have the opportunity to lead impactful projects in a supportive environment, with access to professional development resources and a commitment to employee growth. Our Deeside location provides a unique blend of remote flexibility and in-person collaboration, ensuring you can contribute meaningfully while enjoying a balanced work-life dynamic.
