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Medical Information Specialist I with Swedish
Medical Information Specialist I with Swedish-August 2024
Cambridge
Aug 5, 2026
About Medical Information Specialist I with Swedish

  Job Description

  Medical Information Specialist with Swedish

  Medical Communications is a truly exceptional team at PPD! We work to improve patient health by supplying top-quality medical information services to our clients, patients and health care providers. We engage with health care professionals, regulatory agencies and pharmaceutical clients to help them navigate regulatory, and compliance requirements around the world.  Come join our growing global team of over 900 healthcare professionals providing medical information and education.

  The Medical Information Specialist position provides technical and medical information, and/or performs intake of adverse events / product complaints with high-quality customer service. Analyzes and researches inquiries and documents interactions according to organizational, customer and regulatory guidelines. The information provided will be given to a level in parallel with the individual’s expertise, experience and training.

  At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees.

  Summarized Purpose:

  Provides technical and medical information, and/or performs intake of adverse events/ product complaints with quality customer service. Analyzes and researches inquiries and documents interactions according to organizational, client and regulatory guidelines. The information provided will be given to a level in parallel with the individual’s expertise, experience and training.

  Essential Functions:

  Responds accurately and professionally to technical and medical information inquiries received via phone, email, internet or mail in reference to pharmaceutical or device products.  Processes fulfillments and provides clinical trial information or after-hours on call support.

  Analyzes caller’s questions to formulate an accurate and concise response using client-approved resources and records inquiries and interactions in the appropriate databases following organizational, client and regulatory guidelines.

  Identifies, records and triages adverse events and product complaints according to organizational, client and regulatory guidelines and provides additional support (including follow up) as needed. 

  Maintains thorough knowledge of project and corporate policies and procedures including client products, SOP's, protocols, GCP's, and applicable regulatory requirements.

  Works closely with internal and external client contacts (up to and including members of client management) to resolve complex inquiries. As needed, researches medical literature and drafts responses for such inquiries.

  Qualifications - External

  Education and Experience:  

  Medical, Pharmacy, Biomedical degree or any equivalent to that

  Previous experience that provides the knowledge, skills, and abilities to perform the job will be considered an advantage.

  Proficiency in Swedish

  In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

  Knowledge, Skills and Abilities: 

  Excellent verbal and written communication skills in English and Swedish

  Excellent language skills (comprehension, speaking, reading and writing);

  Fluency skills in Swedish will be required

  Proficient computer and keyboarding skills

  Good interpersonal skills

  Ability to work independently as well as part of a team.

  Ability to interpret client provided complex medical and technical information

  Organizational and time management skills

  Ability to maintain a positive and professional demeanor in challenging circumstances

  Working Environment:

  PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

  Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner

  Able to work upright and stationary for typical working hours

  Ability to use and learn standard office equipment and technology with proficiency

  Able to perform successfully under pressure while prioritizing and handling multiple projects or activities

  May require travel (Recruiter will provide more details)

  Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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