Medical Writer

Celerion; Phoenix (AZ); Remote; USD 70,000 - 100,000; Full time

Job summary

Celerion is seeking a full-time Medical Writer to work remotely, analyzing and interpreting safety results from clinical trials and compiling/editing CSR and other documents. The role requires coordinating with data management, project management, and other departments to ensure accuracy and regulatory compliance.

Responsibilities include peer QC of safety text, timely delivery of scientific reports, and effective communication with clients.

Qualifications

• Bachelor's degree in a medical or scientific field or equivalent experience.
• 1–3 years of hospital/clinical experience or clinical results interpretation.
• Professional writing and editing skills for reporting clinical trial results.
• Detail-oriented, thorough, and methodical.
• Ability to work independently and under pressure.
• Strong communication and interpersonal skills.
• Knowledge of medical/pharmaceutical concepts preferred.

Responsibilities

• Analyze and interpret all types of medical results including vital signs, lab values, adverse events, ECGs and PD endpoints.
• Compile and write Phase I/II CSR documents and safety narratives.
• Perform QC of safety text prior to CSR inclusion and suggest changes.
• Act as project lead to ensure quality and on-time delivery of reports.
• Monitor editorial comments to ensure accuracy and alignment with objectives.
• Ensure deliverables comply with GCP, ICH guidelines and client specs.
• Collaborate with international teams using WebEx, Veeva, MS365, SharePoint and SmartSheet.
• Lead project-related client communication and coordinate with data management and PM teams.
• Participate in activities that support department goals.

Skills

Technical writing

Editing skills

Medical writing

Communication

Attention to detail

Time management

Education

Bachelor's degree in medical/science field

Tools

WebEx

Veeva

Microsoft 365

SharePoint

SmartSheet

Job description

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

We are searching for a full-time Medical Writer to work remotely. This position will analyze and interpret safety results of clinical trials. Compile, write and edit clinical study reports and other industry documents. Confirm accurate classification of events and medications using standardized coding systems.

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

We are searching for a full-time Medical Writer to work remotely. This position will analyze and interpret safety results of clinical trials. Compile, write and edit clinical study reports and other industry documents. Confirm accurate classification of events and medications using standardized coding systems.

Responsibilities

• Analyze and interpret all types of medical results including, but not limited to the following: vital signs, clinical laboratory values, adverse events, electrocardiograms (ECGs), diagnostic procedures, and various pharmacodynamic (PD) endpoints. Compile and write Phase I and Phase II clinical trial documents including, but not limited to the following: clinical study reports (CSRs), stand‑alone safety narratives, and synoptic CSRs.
• Review/evaluate study results to determine whether or not the safety objectives and/or endpoints were met, accurately reflecting the results in the safety text.
• Perform peer QC function of safety text prior to inclusion in the CSR. Review reports for completeness and accuracy assuring that the safety text fits into the CSR as whole and recommending changes or rewriting, as appropriate.
• As the project Report Lead on a multi-disciplinary scientific team, ensoure quality and on‑time delivery of scientific reports.
• Monitor content of editorial comments received prior to incorporation into the report to assure report text comments are accurate and support the objectives and/or endpoints.
• Assure deliverables are compliant with applicable regulatory standards (i.e. Good Clinical Practice, International Conference on Harmonisation guidelines) and client specifications.
• Use technology to work with international teams (e.g., WebEx™, Veeva, Microsoft® 365 applications, SharePoint®, and SmartSheet).
• Lead‑Project‑related client communication
• Interact with internal departments (e.g. data management, project management, business development, etc.).
• Participate in functions required to ensure success of department and/or market segment team.

Requirements

• Bachelor's degree and/or professional license in a medical or scientific field (RN, BS, RPh, MS, MPH) required or equivalent experience.
• 1-3 years experience in hospital/clinical setting or interpreting medical or clinical results.
• Professional writing and editing skills for accurate and concise reporting of clinical trial results; ability to interpret and present data in preparing a coherently written document.
• Detail‑oriented, thorough, and methodical.
• Ability to work without close supervision and ability to work under pressure.
• Ability to multi‑task and to respond rapidly to changing priorities and aggressive timelines.
• Excellent communication/interpersonal skills.
• Knowledge of medical, pharmaceutical, and/or clinical research concepts preferred.

Celerion Values: Integrity Trust Teamwork Respect

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

Note:

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