About our client: Pharmaceutical Company Multinational
Description: Reporting to the Senior Medical Development Manager, this Regional Medical Liaison will have the following responsabilities:
- Maximize value propositions to create value for Patients through medical and scientific projects, services and expertise, with key scientific customers (According to international R&D strategies) Within Therapuetic areas;
- Implement scientific programs in the local territories in collaboration with District Sales Manager Field Operations and Development;
- Run POA RML;- KOL profiles, plans and reports;
- Make Proposals and Other Local study documents for HSR;
- Make educational programs to change medical practice;
- Produce scientific presentations to Physicians and Hospital Departments
- Field feedback: scientific trends, ongoing studies, CI- RML activity tracking
- Support head RML / local Therapeutic Area Leader in Developing the local R & D tactics territory;- Identifiy, Develop and Maintain Collaborative Relationships with current and future KOLs, scientific experts, cooperative study groups and study sites;
- Development and Implementation of local KOL Plans, in line with the local and international KOL strategy;- Create end execute COER engagement plans;
- Implement and disseminate high quality medical and scientific educational programs, giving clinical and scientific presentations at sites / hospitals;
- Identify new research opportunities, Implementation and follow up on scientific HSR and Other Activities, Providing input to the design of local observational research;
- Work with field development operations to Ensure prioritization of site selection, feasibility and support across assigned territories;
- Support ASTs on site with scientific presentations / discussions to create enthusiasm for the scientific program, Understand trial / referral networks and identify enrollment Barriers, Participate in investigator meetings According to approved investigator strategy;
- Ensure society engagement: RML support of international and regional congresses;
- Developsrequired qualitative and quantitative reports;- Ensure Conduct of work in line with compliance Supplements Regulations;
- Deliver targeted internal training for selected topics (eg study update, congress news, latest scientific Developments).
Profile sought
- The ideal candidate Should Have:
- A minimum of 3 years of experience in industry, or a related scientific field in academia, including at least one year in a similar position;
- Experience in sales force, or affiliate Medical Department Clinical Development;
- Willingness to travel;
- A valid driver's license;
- Experience with clinical study management and Conduct;
- Scientific expertise in the therapeutic area;- Native Portuguese and intermediate level of English.
- Knowledge of commercialization and business practices;
- Knowledge of regulatory affairs, drug safety, legal and compliance environment;
- Knowledge of commercialization and business practices;
- Knowledge of regulatory affairs, drug safety, legal and compliance environment;
- Network of customer contacts;
- Medical / scientific research experience.
Several advantages: Patent 521/06;
6 month project.
Reference: TFMM23159Published on 10/05/2012
Location: Lisbon
Type of contract: 6 months
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