Regulatory Affairs Executive

We are looking for an Regulatory Publisher to develop new challenging projects which would include the following responsibilities: - Perform quality control procedures to ensure completion, correctness, navigability, and adherence to regulatory eCTD guidelines. - Perform document management tasks and post-submission activities including file transfer,...

**Job Description - Admission Affairs Executive** **About the company**: Britts Imperial Education Group is an Academic Centre and Education Partner to globally recognized British and European Universities that offer Undergraduate, Postgraduate and Doctoral programs to aspiring learners from across the globe. **Essential Roles and Responsibilities**: As an...

**Required education**: Degree in relevant life science discipline **Required Experience**: 2-4 years relevant experience **Required Technical Skills**: - Lifecycle maintenance experience - Providing support during external and unannounced audits. - Responding to internal requests for technical and/or regulatory information. - Preparation and submission...

The Regulatory Project Assistant (RPA) is responsible for providing project administrative support to the regulatory project team members (regulatory affairs, eTMF operations). The RPA also supports activities within the regulatory website Clinical Trial Information System (CTIS) ensuring completeness and timely entry of information for EU submissions. The...

**Responsibilities and duties** **Requirements**: - Master’s Degree in Biological Science, applied biology or related field. - 3+ years’ practical experience with licenses and certification legal procedures. - Extensive background in data mining and analysis. - Able to understand various botanical and pharmacological common methods and specific...

**Responsibilities**: - To contribute to the production of client administrative documents and reports to be included in regulatory submissions - Compile, or supervise the compilation of regulatory dossiers in accordance with national requirements - LCM, Systems Management and Administration - Document and track regulatory submissions and regulatory...

(India) Looking for experienced regulatory writers **As we are expanding our team, we are thrilled to announce that we are looking for experienced Indian regulatory writers to join our dynamic, collaborative team to engage with biopharmaceutical clients and prepare clinical and safety regulatory documents. This is a full-time, remote, salaried...

**Job ID: ABOJP00037257** **Job Title: Medical Writer II** **Duration: 11/15/2024 to 06/30/2025** **Location: Abbott Park** **IL- 60064 (Remote)** **Remote 20 to 30 hour a week flexibility** **structural heart division** - **Publication or portfolio link must be designated on the resume.**: - Prepare technical document support clinical and medical...

Seeking an Experienced Medical Writer II to Compile and Edit Clinical Study ReportsJob DescriptionWrite, compile, and edit medical documents with minimal supervision.As a seasoned Medical Writer II, you will develop and produce high-quality clinical study reports, narratives, and other medical writing deliverables. This role requires expertise in writing CSR...

**Job Title**: PR Executive **Location**: Remote **Working Hours**: UK Business Hours **Note**: We are looking for an experienced PR professional with prior experience working for UK companies and handling UK clients. **Job Purpose**: As a PR Executive, you will play a key role in supporting the Account Management team in delivering strategic PR campaigns,...