Medical Information Specialist - German & English speaking

EVERSANA

3d•Remote

About The Position

This position is fundamental to building credibility and strengthening relationships with healthcare providers, patients, and industry clients. The position delivers industry-leading services, which include call center staffing for responding to product information requests, identifying and in-taking of adverse events and/or product quality issues, and medical writing. The role is home office based, (full-time position), ideally located in Poland, Ireland, the UK, Italy, Portugal, Germany or Spain and the job holder must be legally eligible to work in the European Union or in the UK.

Requirements

English C1 level is obligatory.
Native German is required.

Nice To Haves

Pharma D / M Pharma but other degrees such as BSc. or MSc. in Pharmacy, BSc.
Call Center, Medical Information, pharmaceutical industry, and clinical experiences including medical writing.
Computer proficiency in Microsoft Word, Excel, and other Window applications.
The utilization of Medical Information Management Systems, Safety Databases, or equivalent.
Exhibits an upbeat attitude, a genuine interest in others, and a sense of humor. Energises others and heightens morale through her/his attitude.
Possesses the ability to develop and articulate ideas and information that generate understanding and create a climate that motivates and encourages others to participate.
Transforms creative ideas into original solutions that positively impact the company’s performance.
Proves to be a professional of unquestionable integrity, credibility, and character who demonstrates high moral and ethical behavior

Responsibilities

Triage and respond to drug information inquiries from physicians, pharmacists, nurses, other health care professionals, and consumers/patients.
Disseminate drug information either verbally or by written correspondence.
Identify adverse events and product complaints during interactions with customers.
Perform intake sufficient to generate initial adverse event and product complaint reports in compliance with EVERSANA-Medical Communications and client SOPs.
Fulfill local Regulatory Authority regulations and requirements for post-marketing adverse event reporting.
Utilise writing skills for adverse event and product complaint narratives during intake as well as medical inquiry custom responses.
Coordinate processes necessary for responding to quality-related complaints. This process may involve interactions with personnel in the following departments: Quality Assurance, Regulatory Affairs, and the complainant.
Utilise drug information skills to critically evaluate medical literature in researching and developing information for written dissemination to healthcare professionals.
Miscellaneous projects including market and competitive product research, system development, sales training projects, and field liaison support.
Medical Writing
On-call responsibilities on an as assigned basis.
All other duties as assigned.