Genmab
Director, Medical Communication & Publications
Genmab, Princeton, New Jersey, us, 08543
At Genmab, we’re committed to building extraordinary futures together, by developing antibody products and pioneering therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in science, we believe that being proudly unique, determined to be our best, and authentic is essential to fulfilling our purpose.
The RoleThe Director of Medical Communications & Publications will be responsible for driving the medical communications and publications strategy for assigned solid tumor assets. The individual will play an integral role in driving publication strategy development, planning, and execution of high-quality scientific publications. This role will work closely with other functions and departments, including Clinical Development, Clinical Operations, Market Access, Biostatistics, Commercial, Corporate Communications, and external collaborators to implement the medical communications strategy. Functioning as a member of the Global Medical Affairs department, this individual will report to the Senior Director of Medical Communications and Publications.
This is a hybrid role that requires onsite presence in Princeton, NJ 60% of the time.
Responsibilities
Lead the Medical Communications and Publication initiatives including abstracts, congress presentations, and manuscripts for assigned solid tumor assets and provide expertise to the matrix team in developing and executing the medical communication plan.
In development of a strategic publication plan, collaborate with cross-functional, key global stakeholders, anticipate risks, and identify solutions for publication planning.
Serve as a therapy area and product expert for both internal and external stakeholders.
Develop scientific content deliverables (including but not limited to, scientific communication platform, PLS, FAQs) and congress content obtaining insights from key stakeholders.
Serve as the subject matter expert on publication-related matters establishing strong working relationships with both internal and external disease-area experts.
Collaborate effectively with cross-functional colleagues and key stakeholders across cultures, backgrounds, and geographies.
Manage annual budget and work within allocated resources, ensuring contracts, SOWs and invoices are submitted accurately and in a timely manner.
Liaise with agency/vendor partners to ensure timely delivery of quality publication.
Bring subject matter expertise in discussions regarding the creation or updates to departmental SOPs.
Qualifications
Advanced degree: PharmD, PhD or MD required. Certification as a Medical Publication Professional (CMPP) desirable.
Knowledge of solid tumors/gynecological cancers is preferred.
7+ years in medical writing and relevant industry work experience and/or expert in medical communications.
Expertise across all aspects of scientific publication strategy, planning and execution during all phases of drug development and commercialization process.
Demonstrate an understanding of clinical research principles and disease state knowledge.
Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements.
Ability to drive and execute within a large matrix, cross-functional team, and work successfully in a fast-paced environment.
Proven ability to think strategically at an enterprise level and make decisions under conditions of ambiguity.
In-depth understanding of good publication practices and guidance (GPP, ICMJE).
Ability to travel domestically and internationally approximately 20% of the time.
For US based candidates, the proposed salary band for this position is as follows: $206,250.00-$343,750.00. The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location.
About You
You are passionate about our purpose and genuinely care about our mission to transform the lives of patients through innovative cancer treatment.
You bring rigor and excellence to all that you do.
You are a generous collaborator who can work in teams with diverse backgrounds.
You are determined to do and be your best.
You are not afraid to grapple with the unknown and be innovative.
You have experience working in a fast-growing, dynamic company (or a strong desire to).
You work hard and are not afraid to have a little fun while you do so.
LocationsGenmab leverages the effectiveness of an agile working environment, when possible, for the betterment of employee work-life balance.
About GenmabGenmab is an international biotechnology company with a core purpose guiding its team to strive towards improving the lives of patients through innovative antibody therapeutics.
Our commitment to diversity, equity, and inclusionWe are committed to fostering workplace diversity at all levels of the company.
#J-18808-Ljbffr
The RoleThe Director of Medical Communications & Publications will be responsible for driving the medical communications and publications strategy for assigned solid tumor assets. The individual will play an integral role in driving publication strategy development, planning, and execution of high-quality scientific publications. This role will work closely with other functions and departments, including Clinical Development, Clinical Operations, Market Access, Biostatistics, Commercial, Corporate Communications, and external collaborators to implement the medical communications strategy. Functioning as a member of the Global Medical Affairs department, this individual will report to the Senior Director of Medical Communications and Publications.
This is a hybrid role that requires onsite presence in Princeton, NJ 60% of the time.
Responsibilities
Lead the Medical Communications and Publication initiatives including abstracts, congress presentations, and manuscripts for assigned solid tumor assets and provide expertise to the matrix team in developing and executing the medical communication plan.
In development of a strategic publication plan, collaborate with cross-functional, key global stakeholders, anticipate risks, and identify solutions for publication planning.
Serve as a therapy area and product expert for both internal and external stakeholders.
Develop scientific content deliverables (including but not limited to, scientific communication platform, PLS, FAQs) and congress content obtaining insights from key stakeholders.
Serve as the subject matter expert on publication-related matters establishing strong working relationships with both internal and external disease-area experts.
Collaborate effectively with cross-functional colleagues and key stakeholders across cultures, backgrounds, and geographies.
Manage annual budget and work within allocated resources, ensuring contracts, SOWs and invoices are submitted accurately and in a timely manner.
Liaise with agency/vendor partners to ensure timely delivery of quality publication.
Bring subject matter expertise in discussions regarding the creation or updates to departmental SOPs.
Qualifications
Advanced degree: PharmD, PhD or MD required. Certification as a Medical Publication Professional (CMPP) desirable.
Knowledge of solid tumors/gynecological cancers is preferred.
7+ years in medical writing and relevant industry work experience and/or expert in medical communications.
Expertise across all aspects of scientific publication strategy, planning and execution during all phases of drug development and commercialization process.
Demonstrate an understanding of clinical research principles and disease state knowledge.
Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements.
Ability to drive and execute within a large matrix, cross-functional team, and work successfully in a fast-paced environment.
Proven ability to think strategically at an enterprise level and make decisions under conditions of ambiguity.
In-depth understanding of good publication practices and guidance (GPP, ICMJE).
Ability to travel domestically and internationally approximately 20% of the time.
For US based candidates, the proposed salary band for this position is as follows: $206,250.00-$343,750.00. The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location.
About You
You are passionate about our purpose and genuinely care about our mission to transform the lives of patients through innovative cancer treatment.
You bring rigor and excellence to all that you do.
You are a generous collaborator who can work in teams with diverse backgrounds.
You are determined to do and be your best.
You are not afraid to grapple with the unknown and be innovative.
You have experience working in a fast-growing, dynamic company (or a strong desire to).
You work hard and are not afraid to have a little fun while you do so.
LocationsGenmab leverages the effectiveness of an agile working environment, when possible, for the betterment of employee work-life balance.
About GenmabGenmab is an international biotechnology company with a core purpose guiding its team to strive towards improving the lives of patients through innovative antibody therapeutics.
Our commitment to diversity, equity, and inclusionWe are committed to fostering workplace diversity at all levels of the company.
#J-18808-Ljbffr