Clinical Science Manager
4 weeks ago
We are seeking a highly skilled Clinical Science Manager to lead our evidence generation and dissemination strategy for assigned products. As a key member of our Clinical Affairs team, you will be responsible for developing and implementing comprehensive publication plans, conducting literature searches and gap analyses, and driving impactful publication development.
Key Responsibilities:
- Lead evidence generation and dissemination strategy for assigned products
- Conduct literature searches and gap analyses to identify evidence gaps used to inform evidence generation and publication plans
- Develop and implement comprehensive publication plans
- Drive impactful publication development (ie, congress presentations, peer-reviewed articles) cross-functionally with Clinical Research, Biostatistics and physician authors
- Provide critical scientific input during publication lifecycle from outline development to galley proof approval
- Engage with cross-functional teams to develop and implement training and dissemination plans for scientific communication materials tailored to various internal and external audiences
- Handle budget, and supervise contracts and vendors associated with publication and communication strategy execution
- Support congress planning, including leading clinical booth activities and scientific evidence gathering
- Mentor junior CSER staff
A minimum of a Bachelor's Degree in Life Sciences, Physical Science, Nursing, Biological Science, or closely related field
A minimum of 5 years of evidence generation and dissemination experience in a relevant clinical or medical affairs industry setting
Strong project management skills with the ability to balance multiple projects
Able to influence others
Strong written and oral communication skills
Strategic mentality and critical analytical skill
Leadership in evidence generation strategy
Proven success in publication planning, development, and execution
Experience supervising medical writers and personnel developing evidence dissemination collaterals for a variety of audiences
Knowledge of Good Clinical Practices and ICMJE standards
Preferred:
PhD/MD/PharmD with industry/academic research experience
8 years of clinical, medical affairs, or related industry setting technical experience
3 years of medical device experience, especially in cardiovascular and/or electrophysiology therapeutic areas
Experience training internal and personnel on clinical evidence supporting medical device products
ISMPP CMPPTM or AMWA MWC credentials
Other:
May require up to 15% travel.
At Johnson & Johnson, we're on a mission to change the trajectory of health for humanity. That starts by creating the world's healthiest workforce. Through cutting-edge programs and policies, we empower the physical, mental, emotional and financial health of our employees and the ones they love.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit .
The anticipated base pay range for this position is 113,000 to 195,500.
This job posting is anticipated to close on September 27, 2024. The Company may however extend this time-period, in which case the posting will remain available on to accept additional applications.
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