Regulatory Specialist Support- German Speaker

hace 1 día


Zaragoza, España Iqvia Argentina A tiempo completo

.Join us on our exciting journeyWe are looking for a Regulatory Specialist to support health care professional attendance to congress and organize medical stands at external educational events, to be part of our international team in IQVIAPosition Purpose:Job DescriptionThis role is responsible for providing support to clients of Compliance Services. The Compliance Services team provide services to the pharmaceutical and med device industries, including Transparency Support and Outsourcing, Grants Management, HCP Screening and Tiering, and HCP Contracting. Our teams need to provide service that is very accurate, timely, and with good customer service.This position is in charge of delivering work every day using our proprietary software. Comfort using technologies is critical. Detailed process orientation and superior communication skills are very important. Experience with pharmaceutical compliance regulations is helpful but not required. Experience with legal contract concepts is helpful.Responsibilities:HCP Contracting and Grants ManagementAfter getting system generated requests, develop contract for HCPs using given templates.Communicate with the HCP regarding contracts, obtain signatures, answer questions.GeneralEffectively communicate requests for required information (e.G., missing information, clarification of information, documentation).Provide updates to team management on status of work and issues addressed.Ensure work delivered is of good quality.Adhere to various policies (i.E., confidentiality, sensitive communication, intellectual property).Respond to client requests for customized reports.Reformat incoming files using Access, Excel, etc. to maintain information in IQVIA usable form.Maintain the integrity and quality of the files.Follow IQVIA quality standards in completing and verifying.Review the client requirements with the Client Service Reps to ensure clarity on each request.Identify data errors.Advise Client Service Reps in creating custom deliverables.Analyze errors and recovery methods for maintaining the files.Competency Requirements:Proficiency in MS-Office, Word, Excel, and Outlook.Strong PC technical skills in using Excel and Access.Good organizational skills and ability to meet deadlines in a time-sensitive environment.Ability to carry out some analysis and information gathering to resolve problems on routine matters.Detail-oriented and able to handle multiple priorities while meeting strict deadlines.Excellent communication and interpersonal skills, with the ability to build strong relationships internally and work within a team environment.Background in Pharmaceutical compliance desirable, but not mandatory.German Speaker and English advanced level.Education, Skills, Experience Desired:Bachelor's degree or equivalent in Life Science is mandatory.Contracts Management or Reports Analyst experience is a plus.5 years or more related work experience.IQVIA is an equal opportunity employer



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