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| Job Location | Sandwich |
| Education | Not Mentioned |
| Salary | Competitive salary |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Contract, full-time |
Are you looking for your nextcontractIf so, afantastic opportunity has justbecomeavailableto workfor a globally establishedPharmaceuticalcompany.We are looking for aProcess Analystto join theirWorldwide Medical & Safetydivisionbasedin Sandwich, Kent.Reportingto the Head of Safety Quality and Risk Management, theProcessAnalystwillmanage processes, compliance, and performance metrics.On offer for the Process Analyst is an initial 12-month contractwith a competitive hourly rate.Responsibilities:Full details of the responsibilities will be included when discussing the role further.Required skillset- Effectiveprocess analytical skills- Detail oriented, independent, and manage processes to both establish timelines and ensure timelines are met. Excellent organizational skills.- Computer applications - The Process Analyst should be competent in various computer applications such as MS Word, Excel, PowerPoint presentations, etc., as well as department systems.- Skills inmatrixpartnerships to effect inclusive and collaborative working relationships with SEPGR colleagues, including engaging Safety Strategy BU Head, Epidemiology Leads and other colleagues supplying sources of safety information.Actively engages WSRO & Safety colleagues in RMCs and Asset teams as needed.- Effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization.- Working effectively when co-located with, AND when remote from, product teams/leaders/managers.- Can handle more than one complex project simultaneously.- Relevant knowledge of Pharmaceutical Company organizational structure, policies, and practices, as applicable to safety Risk Management.- In addition, PAs with RMPL responsibilities:- Project management certification (PMP) andSix SigmaCertification preferred.- Knowledge of Risk Management regulations and drug development process- Ability to interact with and influence a diverse internal and external client base- Proven ability to make sound judgments and willingness to take calculated risks- Demonstrated success in negotiating the environment of a highly matrix-based organization to deliver against complex program plans.- Knowledge of regulatory, commercial and/or medical issues that drive development projects/products.- Experience inbudgetary managementQualification(s)required:- B.SorM.S. inHealthScience(or similar)with significant advanced training- Knowledge ofpharmacovigilance.- Familiarity with management of performance metrics is desirable.- Additionally, for PAs whose responsibilities include RMPL activities, preferred qualificationsincludematrix project management, medical, clinical and lifecycle R&D training and/or experience.Please forward your CV toor phone where we would be happy to tell you more about this exciting opportunity.