Genentech
Sr. Content Design and Execution Lead
Genentech, Los Angeles, California, United States, 90079
The PositionSenior Content Design & Execution Lead
Are you passionate about designing and delivering impactful content to patients, healthcare professionals (HCPs), and access stakeholders? Do you have a strong clinical background and ability to create compelling medical content? If so, we have an exciting opportunity for you to join our team as a Senior Content Design & Execution Lead.
Medical Information and Communications (MI&C), a function in US Medical Affairs (USMA), is dedicated to ensuring that patients have access to medicines by providing scientifically accurate and compelling evidence to healthcare stakeholders. As a senior content design and execution lead, you will play a pivotal role in bridging internal partner functions, collaborating across the dynamic health ecosystem, and ultimately delivering better patient outcomes.
The Opportunity
As a Senior Content Design & Execution Lead, your primary focus will be on designing and executing content creation for multiple channels in specific therapeutic area(s). You will ensure that the medical content provided via medical information and communications channels is impactful, timely, accurate and customer-focused.
Key responsibilities include:
Clinical Expertise: Maintain knowledge in assigned product areas to create engaging, compliant, and patient-centered medical content across various channels.
Problem-solving: Anticipate and address clinical, access, and operational issues impacting Medical Information & Communications and our diverse customer base.
Collaboration: Work with content strategy leads and cross-functional partners to develop new, strategic medical content.
Medical Content Review and Execution: Design and co-create scientifically rigorous and impactful medical content for patients, healthcare providers, and decision-makers, including digital assets and evidence submissions.
Continuous Improvement: Leverage customer feedback to continuously enhance the quality of medical content.
Clinical Guidance: Provide clinical guidance and resolve escalated inquiries from the contact center and PRC/MRC.
Quality Assurance: Ensure clinical accuracy and compliance in contact center calls through quality assurance measures.
Who You Are:
Required:
You have an advanced Clinical/Science degree (e.g. PharmD, PhD, MD) with 6+ years of relevant industry experience in medical communications with 2 or more years clinical experience or equivalent experience.
You have significant experience with all aspects of healthcare communications activities and have demonstrated ownership of significant expertise and creativity in healthcare communications.
You have experience in creating compelling content disseminated via many medical affairs channels.
You have an execution mindset with strong organizational and project management skills to ensure content is delivered on time and within budget.
Superb collaboration and communication (oral and written) skills in developing strong partnerships with cross-functional peers.
Substantive understanding and exposure to corporate legal and compliance groups, and are knowledgeable of issues related to GCP, OIG, US Regulatory/FDA requirements, drug access, and other guiding or controlling elements of our business.
Preferred:
Ability to influence without authority.
Able to prioritize based on business and customer needs.
Proven track record of meeting or exceeding objectives and goals.
Embraces an agile mindset to create necessary processes to get things done.
Embraces a growth mindset to adapt and iterate in order to meet customer needs.
Knows how to organize activities effectively to achieve impactful outcomes.
Relocation benefits are available for this posting.
This position is based in South San Francisco and presence is needed on-site at our Genentech Campus.
The expected salary range for this position based on the primary location of South San Francisco, California is $160,900 and $298,900. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Benefits
Genentech is an equal opportunity employer, and we embrace the increasingly diverse world around us. Genentech prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status, and veteran status.
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Are you passionate about designing and delivering impactful content to patients, healthcare professionals (HCPs), and access stakeholders? Do you have a strong clinical background and ability to create compelling medical content? If so, we have an exciting opportunity for you to join our team as a Senior Content Design & Execution Lead.
Medical Information and Communications (MI&C), a function in US Medical Affairs (USMA), is dedicated to ensuring that patients have access to medicines by providing scientifically accurate and compelling evidence to healthcare stakeholders. As a senior content design and execution lead, you will play a pivotal role in bridging internal partner functions, collaborating across the dynamic health ecosystem, and ultimately delivering better patient outcomes.
The Opportunity
As a Senior Content Design & Execution Lead, your primary focus will be on designing and executing content creation for multiple channels in specific therapeutic area(s). You will ensure that the medical content provided via medical information and communications channels is impactful, timely, accurate and customer-focused.
Key responsibilities include:
Clinical Expertise: Maintain knowledge in assigned product areas to create engaging, compliant, and patient-centered medical content across various channels.
Problem-solving: Anticipate and address clinical, access, and operational issues impacting Medical Information & Communications and our diverse customer base.
Collaboration: Work with content strategy leads and cross-functional partners to develop new, strategic medical content.
Medical Content Review and Execution: Design and co-create scientifically rigorous and impactful medical content for patients, healthcare providers, and decision-makers, including digital assets and evidence submissions.
Continuous Improvement: Leverage customer feedback to continuously enhance the quality of medical content.
Clinical Guidance: Provide clinical guidance and resolve escalated inquiries from the contact center and PRC/MRC.
Quality Assurance: Ensure clinical accuracy and compliance in contact center calls through quality assurance measures.
Who You Are:
Required:
You have an advanced Clinical/Science degree (e.g. PharmD, PhD, MD) with 6+ years of relevant industry experience in medical communications with 2 or more years clinical experience or equivalent experience.
You have significant experience with all aspects of healthcare communications activities and have demonstrated ownership of significant expertise and creativity in healthcare communications.
You have experience in creating compelling content disseminated via many medical affairs channels.
You have an execution mindset with strong organizational and project management skills to ensure content is delivered on time and within budget.
Superb collaboration and communication (oral and written) skills in developing strong partnerships with cross-functional peers.
Substantive understanding and exposure to corporate legal and compliance groups, and are knowledgeable of issues related to GCP, OIG, US Regulatory/FDA requirements, drug access, and other guiding or controlling elements of our business.
Preferred:
Ability to influence without authority.
Able to prioritize based on business and customer needs.
Proven track record of meeting or exceeding objectives and goals.
Embraces an agile mindset to create necessary processes to get things done.
Embraces a growth mindset to adapt and iterate in order to meet customer needs.
Knows how to organize activities effectively to achieve impactful outcomes.
Relocation benefits are available for this posting.
This position is based in South San Francisco and presence is needed on-site at our Genentech Campus.
The expected salary range for this position based on the primary location of South San Francisco, California is $160,900 and $298,900. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Benefits
Genentech is an equal opportunity employer, and we embrace the increasingly diverse world around us. Genentech prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status, and veteran status.
#J-18808-Ljbffr