Scientific Review Manager
Johnson & Johnson
Panama
hace 1 día

At Johnson & Johnson, the largest healthcare company in the world, we come together with one purpose : to profoundly change the trajectory of health for humanity.

Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years.

Regardless of your race, belief, sexual orientation, religion or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.

When You Join Johnson & Johnson, Your Next Move Could Mean Our Next Breakthrough

The Scientific Review Manager is responsible for the Scientific material regional strategy co-creation and support in content development, approval and dissemination through multi-channels including MSLs, Scientific Advisors, scientific websites and other.

Management, with IT partnership, of technology tools with the purpose to provide the most updated content in time manner.

Responsible for all strategic and operational team focusing on Medical Affairs needs and scientific development guidance.

Insights generation according to content dissemination analysis and trends resulting in customized / segmented scientific content.

Compliance, training, communication, and Quality Assurance to ensure a compliant and operational excellence. Responsible for the development of all employees within the department including management development and training to meet current and future business needs.

Provide an environment, which encourages the company's commitment to equal employment opportunity and the value of a diverse work force.

Responsibilities :

Scientific content co-creation strategy, development and dissemination according to regional and local needs :

Mapping of regional and local scientific scenario

Development plan with solutions to attend the scientific needs including : Content type, Channels, Timeframe agility

Management of scientific content development and approval operation guaranteeing the quality, relevance, and compliance.

Approval flow governance

Management of development and maintenance of process and systems documentation to support the operation internally and with the stakeholders.

Guarantee the support to all specialists in order to obtain access to product knowledge

Develop the team to follow the company strategy

Actively participation in strategy therapeutic area discussions

Provide ideas and solutions to attend the key scientific messages

Co-create with therapeutic areas strategic plan

Align with the scientific specialist team the customer needs, timeframe, and operation.

Share plan implementation results

Partner with other scientific affairs area to guarantee a consistent plan and continuity

Negotiate with partners to provide the best and most complete solutions to the therapeutic areas

Partner with internal customers / vendors in the design and development of change management, training and training materials (training plan, course outline, knowledge assessments, instructional materials and tools).

Management of monitoring & evaluation of training effectiveness to ensure programs meet customer needs; tailor programs as needed

Maximize user learning experience

Define and share frequent KPIs dashboards to provide oversight to the stakeholders

Provide corrective and preventive actions to enhance the KPIs

Establish ongoing opportunities to partner with key stakeholders, leadership including conducting VOC surveys to address user feedback and proactively resolve issues

Create and execute short- and long-term communication strategy to drive understanding & change management considering :

System communication such as outage, improvements

Monitors and ensures appropriate use of policies, processes and procedures including : Development, documentation and implementation of corrective action plans for resolution of problematic issues

Requirements : Bachelor Degree

Bachelor Degree

Master’s degree in sciences, preferably in Life Sciences (e.g., Medicine, Pharmacy, Biology or Biochemistry)

Fluency in English

Spanish and Portuguese desired.

Minimum of 4 years of experience in pharmaceutical industry, in areas as Medical Affairs or Regulatory Affairs.

Vast Scientific background.

Skills : Strategic thinking.

Strategic thinking.

Quality and detail oriented.

Capability to connect with different stakeholders providing a cooperative and high-performance environment.

High learning and change capability.

Effective leadership skills and proven ability to foster team productivity and cohesiveness.

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