At Zoe MedCare, we specialize in delivering exceptional medical writing services to pharmaceutical and biotech companies. Our focus areas include regulatory writing and medical communication tailored to support the drug development process. With a commitment to clarity, accuracy, and compliance, we produce critical documents such as Clinical Study Reports (CSR), Investigator Brochures (IB), and CTD modules.
Join a team that values precision and innovation in transforming scientific data into comprehensible formats.
Job Responsibilities
As a Medical Writer at Zoe MedCare, you will:
- Prepare regulatory documents such as Clinical Study Reports (CSR), Investigator Brochures (IB), and CTD modules (2.5, 2.7.3, and 2.7.4).
- Ensure accuracy, compliance, and clarity in all written materials.
- Develop and execute communication strategies tailored to client needs.
- Collaborate with cross-functional teams to maintain consistency in messaging.
- Work independently to meet deadlines while adhering to the highest quality standards.
This is a part-time, remote role that offers flexibility while enabling you to make significant contributions to the pharmaceutical and biotech industries.
Qualifications
To excel in this role, candidates should possess the following:
- A master’s degree in a relevant field such as Life Sciences, Pharmacy, or Medicine.
- Strong communication skills and attention to detail.
- Experience in medical writing, including regulatory and medical communication.
- Familiarity with regulatory requirements in drug development.
- Ability to work independently in a remote setting.
Training or certifications in pharmaceutical writing are an added advantage.
Key Skills
- Expertise in regulatory writing and document preparation.
- Proficiency in medical communication and clinical research.
- Strong organizational and analytical skills.
- SEO-friendly writing experience (preferred).
