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Director Medical Affairs I&I CEE Job. Job in Bratislava in Celgene Corporation. Nelest.com
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Director Medical Affairs I&I CEE Job

col-narrow-left   

Job ID:

23225

Location:

Bratislava 

Job function:

Marketing, Sales
col-narrow-right   

Posted:

03.11.2016

Employment Type:

Full time

Industry:

Healthcare / Pharma
col-wide   

Title:

Director Medical Affairs I&I CEE Job

Job Description:

Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we look for talented people to grow our business, advance our science and contribute to our unique culture.

This role is the lead role for the Medical Affairs department for I&I and encompasses leadership roles in knowledge, strategy, and management. The role incorporates direct executional activities as well as leadership of the I&I Medical Affairs team in the CEE countries. Initially, the focus will be on Slovakia, Slovenia, Czech Republic and Croatia however, there is a strong chance to enter additional countries in the region. This will include the building and maintenance of an organization designed to optimize the clinical data platform in the these countries and maximize the dissemination of scientific and medical knowledge for I&I therapeutic areas of interest to all key stakeholder groups. Responsibilities will include, but are not limited to, the following:

Medical Affairs
The incumbent will act as the Medical Affairs leader for I&I therapeutic areas of interest in the CEE countries, providing medical and scientific expertise, leading the development and implementation of the CEE clinical platform, leading and managing the field medical team (RML), acting as strategic partner to cross functional CEE affiliate colleagues, and liaising with EU and HQ personnel in the development and execution of key imperatives and stakeholder relations.

Responsibilities for the Medical Affairs Director:
Act as full partner to cross functional brand team for brand planning and brand leadership.
Ensure execution of agreed medical affairs plan, by direct activities and by leadership of the I&I Medical Affairs team.
Manage and ensure appropriate team execution and development, including supervising and providing a medical insight to all training programs, working to agree executional plan and ensuring a proper follow-up.

Responsibilities for the Medical Affairs department include:
Identify, develop and maintain collaborative relationships with current and future key thought leaders and healthcare stakeholders in disease states of strategic importance to Celgene.

Provide regional perspective and imperatives on KOL/stakeholder development.

Act as key interface to thought leaders (or external partners) in order to disseminate clinical information, medical education opportunities/materials, and facilitate scientific exchange.

Provides medical input to the strategy, planning and review of clinical publications, and review of external clinical research proposals involving the Company products.

Evaluate and profile potential investigators/sites to participate in clinical development studies and/or other opportunities for research collaborations utilising Celgene's pipeline compounds.

Initiate, coordinate and provide clinical protocol expertise to physician investigators by collaborating, reviewing, evaluating and assisting with the development, implementation and publication of Investigator Initiated Trials (IITs).

Assist in the reconnaissance of Market landscape determination and competitive intelligence including therapeutic trends and unmet needs within the appropriate disease states and marketplace.

Work cross functionally to help develop appropriate/pertinent tactical activities and resource materials to be distributed upon request to physicians in targeted disease areas.

Maintain scientific expertise in Therapeutic Area concordant with current knowledge and practice.

Supports general clinical and medical affairs activities involving product evaluation and implementation of franchise business strategies opportunities.

Assists in identifying new marketing opportunities.

Supports the development of training programs for RML and Commercial colleagues, as appropriate.

Engage actively and extensively in cross-functional collaboration with all internal stakeholders

Lead all activities within the CEE Compliance requirements. Have the ability to respond to any adverse queries, events or complaints.

Responsibility for ensuring I&I medical operations work within our agreed compliance framework and SOPs with final signatory responsibility for the code of practice.

Liaise and work closely with the Drug Safety Team who have the key responsibility to report and manage adverse events and risk management.
Responsibility for contributing medical / clinical component of HTA submissions and front facing reimbursement and other agencies on medical / clinical matters as appropriate.

Clinical Research
Activities will be principally CEE based, liaising with HQ personnel in the development and execution of key imperatives and stakeholder relations as required.

The review of IITs and potential IITs will be a key part of this role.

Study related activities:
Main activities, as directed:
Develop CEE specific research plan aligned to CEE strategy to support the development of data to optimize scientific exchange
Develops credible relationships with investigators/KOLs.
Support local CRO /CRA activities, providing medical insights , as needed.
Facilitate contacts between CRO/CRA and investigators.
Attend to meeting related to study implementation when requested or deemed useful.

Job Requirements:


- Therapy area expertise in dermatology and immunology would be a key advantage.

- Excellent written and verbal communication skills and interpersonal skills. Ability to advise, persuade and negotiate with colleagues in a supportive and encouraging fashion.

- Strong interpersonal skills commensurate with the need to effectively manage teams of peers and to work closely with both external physicians/scientists and numerous in-house support groups. Must be able to relate effectively to people at all levels of the organisation.

- Strong leadership skills, collaboration and team worker.

- Able to apply scientific knowledge and understands the role of complementary functions within the team.

- Excellent knowledge of local and international guidelines

- Competent to work in cross functional and multinational teams.

- Demonstrated ability to maintain scientific credibility while being commercially supportive, and to communicate scientific results and effectively respond to data queries from customers and/or consultants.

*MONEU
*LI-MD2

Travel: Yes, 50 % of the Time

Company Info
Celgene Corporation
86 Morris Avenue
Summit, NJ, United States

Phone: +1-908-673-9000, +41 32 729 85 00, 1-908-673-9800, 1-908-673-9800
Web Site: www.celgene.com

Company Profile

Company Info


Celgene Corporation
86 Morris Avenue
Summit, NJ, United States
Phone: +1-908-673-9000, +41 32 729 85 00, 1-908-673-9800, 1-908-673-9800
Web Site: www.celgene.com

Director Medical Affairs I&I CEE Job

col-narrow-left   

Job ID:

23225

Location:

Bratislava 

Job function:

Marketing, Sales
col-narrow-right   

Posted:

03.11.2016

Employment Type:

Full time

Industry:

Healthcare / Pharma
col-wide   

Title:

Director Medical Affairs I&I CEE Job

Job Description:

Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we look for talented people to grow our business, advance our science and contribute to our unique culture.

This role is the lead role for the Medical Affairs department for I&I and encompasses leadership roles in knowledge, strategy, and management. The role incorporates direct executional activities as well as leadership of the I&I Medical Affairs team in the CEE countries. Initially, the focus will be on Slovakia, Slovenia, Czech Republic and Croatia however, there is a strong chance to enter additional countries in the region. This will include the building and maintenance of an organization designed to optimize the clinical data platform in the these countries and maximize the dissemination of scientific and medical knowledge for I&I therapeutic areas of interest to all key stakeholder groups. Responsibilities will include, but are not limited to, the following:

Medical Affairs
The incumbent will act as the Medical Affairs leader for I&I therapeutic areas of interest in the CEE countries, providing medical and scientific expertise, leading the development and implementation of the CEE clinical platform, leading and managing the field medical team (RML), acting as strategic partner to cross functional CEE affiliate colleagues, and liaising with EU and HQ personnel in the development and execution of key imperatives and stakeholder relations.

Responsibilities for the Medical Affairs Director:
Act as full partner to cross functional brand team for brand planning and brand leadership.
Ensure execution of agreed medical affairs plan, by direct activities and by leadership of the I&I Medical Affairs team.
Manage and ensure appropriate team execution and development, including supervising and providing a medical insight to all training programs, working to agree executional plan and ensuring a proper follow-up.

Responsibilities for the Medical Affairs department include:
Identify, develop and maintain collaborative relationships with current and future key thought leaders and healthcare stakeholders in disease states of strategic importance to Celgene.

Provide regional perspective and imperatives on KOL/stakeholder development.

Act as key interface to thought leaders (or external partners) in order to disseminate clinical information, medical education opportunities/materials, and facilitate scientific exchange.

Provides medical input to the strategy, planning and review of clinical publications, and review of external clinical research proposals involving the Company products.

Evaluate and profile potential investigators/sites to participate in clinical development studies and/or other opportunities for research collaborations utilising Celgene's pipeline compounds.

Initiate, coordinate and provide clinical protocol expertise to physician investigators by collaborating, reviewing, evaluating and assisting with the development, implementation and publication of Investigator Initiated Trials (IITs).

Assist in the reconnaissance of Market landscape determination and competitive intelligence including therapeutic trends and unmet needs within the appropriate disease states and marketplace.

Work cross functionally to help develop appropriate/pertinent tactical activities and resource materials to be distributed upon request to physicians in targeted disease areas.

Maintain scientific expertise in Therapeutic Area concordant with current knowledge and practice.

Supports general clinical and medical affairs activities involving product evaluation and implementation of franchise business strategies opportunities.

Assists in identifying new marketing opportunities.

Supports the development of training programs for RML and Commercial colleagues, as appropriate.

Engage actively and extensively in cross-functional collaboration with all internal stakeholders

Lead all activities within the CEE Compliance requirements. Have the ability to respond to any adverse queries, events or complaints.

Responsibility for ensuring I&I medical operations work within our agreed compliance framework and SOPs with final signatory responsibility for the code of practice.

Liaise and work closely with the Drug Safety Team who have the key responsibility to report and manage adverse events and risk management.
Responsibility for contributing medical / clinical component of HTA submissions and front facing reimbursement and other agencies on medical / clinical matters as appropriate.

Clinical Research
Activities will be principally CEE based, liaising with HQ personnel in the development and execution of key imperatives and stakeholder relations as required.

The review of IITs and potential IITs will be a key part of this role.

Study related activities:
Main activities, as directed:
Develop CEE specific research plan aligned to CEE strategy to support the development of data to optimize scientific exchange
Develops credible relationships with investigators/KOLs.
Support local CRO /CRA activities, providing medical insights , as needed.
Facilitate contacts between CRO/CRA and investigators.
Attend to meeting related to study implementation when requested or deemed useful.

Job Requirements:


- Therapy area expertise in dermatology and immunology would be a key advantage.

- Excellent written and verbal communication skills and interpersonal skills. Ability to advise, persuade and negotiate with colleagues in a supportive and encouraging fashion.

- Strong interpersonal skills commensurate with the need to effectively manage teams of peers and to work closely with both external physicians/scientists and numerous in-house support groups. Must be able to relate effectively to people at all levels of the organisation.

- Strong leadership skills, collaboration and team worker.

- Able to apply scientific knowledge and understands the role of complementary functions within the team.

- Excellent knowledge of local and international guidelines

- Competent to work in cross functional and multinational teams.

- Demonstrated ability to maintain scientific credibility while being commercially supportive, and to communicate scientific results and effectively respond to data queries from customers and/or consultants.

*MONEU
*LI-MD2

Travel: Yes, 50 % of the Time
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