Analyst Ii, Regulatory Medical Writing X-ta

7 days ago

Toronto, Canada Johnson & Johnson Full time

**Job Function**:
Medical Affairs Group

**Job Sub**Function**:
Medical Writing

**Job Category**:
Professional

**All Job Posting Locations**:
Toronto, Ontario, Canada

**Analyst II, Regulatory Medical Writing X-TA**

**We are searching for the best talent for Analyst II, Regulatory Medical Writing, X-TA located UK, EU or Canada (Hybrid) (2 available positions).**

As Analyst II, Regulatory Medical Writing X-TA, you will support across one or more of our therapeutic areas (Oncology, Immunology, Neuroscience, Cardiopulmonary, Specialty Ophthalmology) within our Regulatory Medical Writing team, to author diverse regulatory medical writing documents. Hybrid (3 days onsite per week) is preferred. _Remote work options may be considered on a case-by-case basis and if approved by the Company. _

United Kingdom - Requisition Number: R-021736

EU (Belgium, France, Germany, Netherlands) - Requisition Number: R-023564

Canada - Requisition Number: R-023566

**Purpose**:

- Develop within the medical writing role within the pharmaceutical industry.
- Work in a team environment and matrix.
- Learn and use internal systems, tools, and processes.
- Write and coordinate basic documents and help to prepare more complex documents.
- Perform routine tasks per established procedures.

**You will be responsible for**:

- Write and coordinate clinical documents such as protocols, clinical study reports, tables of studies, narratives, and investigator’s brochures with oversight.
- Perform document QC, literature searches, and other tasks.
- Work in a matrix environment and gain an understanding of the medical writing responsibilities on project teams.
- Partner with experienced colleagues on document planning, timelines, and content development according to internal processes.
- Participate in or lead cross-functional document planning and review meetings independently or with oversight.
- May participate in initiatives to improve medical writing processes and standards.
- Regularly meet with manager and mentors and attend departmental meetings.

**Qualifications / Requirements**:

- A university/college degree in a scientific discipline is the minimum requirement, with an advanced degree (eg, Master’s degree, PhD, MD) preferred.
- At least 2 years of relevant pharmaceutical/scientific experience is required.
- Strong oral and written communication skills in English.
- Ability to understand, interpret, and summarize scientific or medical data.
- Ability to function in a team environment and to build solid and positive relationships with cross‐functional team members.
- Demonstrated problem-solving skills.
- Strong attention to detail.
- Strong time management and project/process management skills.
- Demonstrated learning agility.
- Sound knowledge of Microsoft Office programs (eg, Microsoft Word, Excel, PowerPoint, Outlook).

**Benefits**

LI-Hybrid

LI-Remote

**The anticipated base pay range for this position is**:
62,000-100,050 CAD

Additional Description for Pay Transparency:

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