**Medical Writing Expertise**
We are seeking an accomplished Medical Writer to prepare high-quality documents that support our clients' clinical development programs.
**Key Responsibilities:**
* Development of clinical and regulatory documents, including integrated reports, protocols, investigator brochures, regulatory submissions, manuscripts for publication, and other necessary documents.
* Liaison with clients, external consultants, colleagues, and review of current literature sources to ensure the document is developed in alignment with the client's goals, local regulations, and Good Clinical Practice (GCP).
* Collaboration with cutting-edge early phase technology across multiple therapeutic areas based on local and international client requirements.
**Required Skills and Qualifications:**
* A degree in life sciences or equivalent, and a higher degree in a related field (e.g., MSc or PhD) is required.
* Must have experience writing regulatory documentation, including Clinical Study Reports and Clinical Protocols.
* Prior experience in product development from working within biotech or Medical Writing experience in a CRO is preferred.
**Benefits:**
We offer a supportive work environment, flexible working options, paid parental leave, flexible leave entitlements, wellness programs, and ongoing development opportunities.
Our team values diversity, equity, and inclusion. We welcome people who identify as LGBTIQ+, have a disability, or have caring responsibilities.
**About Our Team:**
Our team members are passionate about working in clinical research and biotech. We strive to create a workplace where everyone is treated fairly and with respect.