Associate Scientific Director KME

About the role

The Associate Scientific Director (ASD) supports the development of medical education for both professional and consumer audiences. This role involves providing support for medical, scientific, and strategic planning, content development, and execution. The ASD collaborates with a Scientific Director to develop new activity concepts, proposals, and content, and works closely with faculty, cross-functional teams, and key opinion leaders.

Responsibilities

• Supports the development of medical education programs for medical professionals and consumers
• Develops slides and handouts in PowerPoint format
• Reviews posters/presentations from annual meetings pertinent to content development
• Performs necessary literature searches to verify scientific data and ensure accuracy and completeness of bibliography
• Ensures content is medically/scientifically accurate and compliant
• Collaborates with faculty for content changes and updates to all content during development
• Establishes clear communication and effective relationships with contributing faculty and educational partners
• Ensures delivery of quality products efficiently under multiple timelines
• Assists in social media campaigns for live, online, and enduring activities
• Helps to oversee development of ARS and pre/post-test questions for educational activities
• Contributes to analyzing outcomes and survey data to generate presentations, reports, and abstracts for industry meetings and publications
• Provides insight regarding evidence-based medical information, emerging therapies, practice-related issues, and medical education and pharmaceutical industry trends for strategic business planning
• Reads medical literature, remains aware of late-breaking news/publications, and routinely observes competitive educational activities to ensure expertise in therapeutic areas and alignment
• Initiates and maintains relationships with program faculty in areas of expertise to ensure educational alignment and identify additional educational opportunities
• Performs additional supportive tasks to ensure timely execution of all project deliverables
• Provides input/feedback to contribute to overall project success; e.g., help identify target audience, suggest ways to increase reach, etc.
• Performs other duties and responsibilities as assigned

Requirements

• Able to prioritize multiple tasks and willing to accommodate to the changing demands of each project
• Knowledge of industry compliance/guidelines (OIG, HIPAA, PhRMA, ACCME)
• Basic knowledge of Microsoft Office Suite, EndNote, and PubMed
• Excellent relationship building skills
• Excellent time management skills with a proven ability to meet deadlines
• Excellent verbal and written communication skills
• Excellent organizational skills and attention to detail
• Strong analytical and problem-solving skills

Qualifications

• Master’s degree or above in science, writing, or related field required or equivalent combination of education and experience (MD, PhD, PharmD, DO preferred)

Skills

• Able to prioritize multiple tasks and willing to accommodate to the changing demands of each project
• Knowledge of industry compliance/guidelines (OIG, HIPAA, PhRMA, ACCME)
• Basic knowledge of Microsoft Office Suite, EndNote, and PubMed
• Excellent relationship building skills
• Excellent time management skills with a proven ability to meet deadlines
• Excellent verbal and written communication skills
• Excellent organizational skills and attention to detail
• Strong analytical and problem-solving skills

Benefits

No specific benefits are mentioned in the job posting.

Pay

No specific pay details are provided in the job posting.

Schedule

No specific schedule details are provided in the job posting.