Scientific Content Strategy Specialist Fixed Term - Bogota, Colombia - Johnson & Johnson

Johnson & Johnson

Empresa verificada

Bogota, Colombia

hace 1 semana

Publicado por:

Carolina González

beBee Recruiter

Descripción

At Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities, and forward progress.

That's why for more than 135 years, we have aimed to keep people well at every age and every stage of life.

Today, as the world's largest and most broadly based healthcare company, we are committed to using our reach and size for good.

We strive to improve access and affordability, create healthier communities, and put a healthy mind, body, and environment within reach of everyone, everywhere.

Every day, our more than 140,000 employees across the world are blending heart, science, and ingenuity to profoundly change the trajectory of health for humanity.

Diversity, Equity & 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 Move Could Mean Our Next Breakthrough.

We are searching for the best talent for Scientific Content Strategy Specialist FIXED TERM to be in Bogota.

Purpose:

As a
Scientific Content Strategy Specialist FIXED TERM you will be responsible for the development of scientific materials and approval process, supporting technology and operational functions focusing on Medical Affairs needs.

You will be responsible for:

To be responsible for the development and maintenance of process and system documentation to support the operation internally and with the stakeholders, with supervisor's support and the system process oversight and licenses.
To support, guide and act as moderator in the review and approval flows of scientific materials, including organizing and participating in meetings on the topic, participating in the Scientific Material Planner equivalent of his/her respective therapeutic area (TA) to align the future demand and to contribute with the TA ́s in the plan.
To support creation and execution of short

- and long-term communication strategy for the Scientific Review to drive understanding & change management.

Qualifications:

Required:

Bachelor's degree in sciences degree or equivalent required, preferably in Life Sciences
Fluency in English language
Minimum of 1years of experience in the pharmaceutical industry, in areas as RA (regulatory affairs), or MAF (Medical Affairs) or Quality

Desired: