Paralegal staff at Henleaze Law UK (2022-02 – Present)
Remote Paralegal Staff Responsibilities for UK Solicitors. As a Remote Paralegal Staff working with UK solicitors, have been responsible for the following tasks:
- Collecting Necessary Client Documents: Gathering important documents from clients required for their legal cases.
- Communicating with Clients: Speaking with clients to understand the basic details of their case related to various immigration options.
- Compiling Document Lists: Creating lists of documents needed for specific applications based on individual client requirements.
- Creating Application Forms: Drafting application forms for submission to relevant authorities.
- Crafting Cover Letters and Statements: Writing cover letters and statements on behalf of clients, ensuring accuracy through client proofreading.
- Handling Appeal Cases: Working on cases where appeals are necessary, collecting evidence to challenge refusals.
- Uploading Documents: Submitting final documents electronically to the Home Office.
- Following Up with MPs: Communicating with Members of Parliament (MPs) to inquire about pending decisions.
- Lodging Complaints: Submitting complaints when decisions are incorrect or when documents are missing or mishandled.
- Providing Daily Reports: Sharing daily progress reports with the line manager.
Assistant Product Manager at High-Q Pharmaceuticals (2014-09 – 2015-09)
- Preparing marketing strategy for the brands.
- Plan, monitor and manage marketing budget.
- Training and motivating Field Sales team to ensure they are equipped with complete product knowledge.
Clinical Trials Monitor: Phase 3 & 4 studies at GlaxoSmithKline, Pakistan (2013-11 – 2014-08)
- Coordinate with the collection, distribution, and storage of data obtained during clinical research trials, for the testing of drugs and medical products.
- Ensured that trials stay on track with clinical objectives and complies with federal regulations.
- Performed CRF review, query generation and resolution against established data review guidelines data management systems.
- Identified and completed follow-up of Serious Adverse Events at assigned study sites.
- Ensured the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.
- Ensure that the Site Regulatory Documents are complete and current through trial.
Internship at ABBOTT (2011-01 – 2011-02)
- One month internship in QA/QC and Production Dept.
