The position : Medical Advisor

Qualifications :

- Medical Doctor (MBBS) with MD (Pharmacology) degree and minimum 2 (two) years of working experience as Medical Advisor in a pharmaceutical / ingredient company.

- Required to have strong scientific knowledge of Clinical trails and research. At least 2-3 years of experience of writing clinical trial publications in a pharmaceutical / ingredient company. Good collaboration with internal and external stakeholders as well as good in communication and negotiation.

- Need to have - can-do-attitude- to achieve the goals and making things happen despite obstacles and having a good business understanding of probiotics would be advantageous.

Key Responsibilities Of The Position :

- Ensure to conduct Clinical trails, co-ordinate with CRO for timely execution of clinical trails with desired results

- Publish the papers. Prepare Dossier's.

- To assist marketing efforts by actively participating in clinical trials, meetings, conferences, updates, CME's and publications

- Contribute to new product launches by proper and timely execution of regulatory processes and contribute to positioning through literature surveys, clinical trials and pre-launch customer perception mapping.

- Ensure that the profile of Sanzyme Biologics remains high amongst stakeholders like doctors, patients, paramedics, associations etc. by developing and maintaining a close rapport through liaison and networking

- To help educate and train field and marketing personnel regarding all aspects of disease,product and therapy relevant to the promotional strategy

- To ensure close and positive interaction between medical and marketing to help sharpen promotional strategies and their implementation

- To assist the regulatory affairs personnel in ensuring that all promotional activities.

- To work closely with major institutions by providing medical support, advisory board support and active involvement in clinical research programs

- Be responsive and proactively alert to issues related to competitor activities and facilitate effective and timely corrective actions by responsible persons

- Contribute to new product launches by proper and timely execution of regulatory processes and contribute to positioning through literature surveys, clinical trials and pre-launch customer perception mapping.

- Ensure and maintain customer focus and regular field visits to ensure the KOL contacts.

- Active support and participation in all the major activities like Medical Updates for the assigned product by designing scientific programs and also involving the KOLs in major activities.

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