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If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! location: Whippany, New Jersey job type: Contract salary: $63.12 - 74.26 per hour work hours: 9 to 5 education: Doctorate responsibilities: POSITION SUMMARY- The US Medical Affairs Communication/Communication Platform Development-Content Generation Lead is a strategic partner of the US Medical Affairs Communication team responsible for supporting the development and execution of the medical communications strategy across the assigned therapeutic portfolio. Incumbent is involved in the development of medical communications Scientific Communication Platform (SCP) and Leads the Integrated Communication Platform Development and Content Generation which may include, but is not limited to scientific slide decks, field medical tools, training materials, congress-related activities, websites/tools. This energetic individual will work with many different teams within and outside of Medical Affairs to drive the development and review of external facing content while ensuring accuracy and scientific balance. As part of the medical review team, the AD is responsible for conducting comprehensive medical review and clearance of US promotional and non-promotional materials. The AD leverages his/her functional and technical expertise to assist in improving organizational effectiveness of the MAC/Communication Platform Development/Content Generation function. POSITION DUTIES & RESPONSIBILITIES In close collaboration with Global and USMA colleagues, leads the strategy and execution of medical communications Scientific Communication Platform (SCP) and the Integrated Communication Platform Development (ICPD)/Content Generation (CG), including but is not limited to scientific slide decks, field medical tools, training materials, congress-related activities, websites/tools.Maintain in-depth knowledge of medical communications trends and materials (scientific platform, core slide decks, scientific communication plans, digital communication plans) and can drive updates/revisions to these materials.Maintain the scientific accuracy and robustness of the information included in the SCP and Core Communication Objectives (CCOs) for assigned products, and in close collaboration with the cross-functional team supports the development of new SCPs for new products.Support medical review during the promotional and non-promotional (e.g., disease state) commercial material review, as well as medical affairs material review, for assigned brands. Provides the comprehensive medical review of advertising and promotional materials on their assigned therapeutic areas, ensuring that information is scientifically accurate and medically appropriate. Collaborates with legal and regulatory to develop a consistent process and ensure consistent reviews of promotional materials.Drive post-congress support including liaising with competitive intelligence and post-congress integration of learnings into medical materials and communication plans.Assist in scientific or medical content development for the Field Medical Learning and Development Team for training materials for assigned therapeutic area.Ensure that assigned medical communication projects remain on strategy, within budget, and are executed promptly.Collaborates with key stakeholders to identify data gaps and opportunities for creation and deployment of Medical Affairs tools introducing innovative ways to drive HCP awareness and adoption to medical initiatives.Ensures that information systems used by Medical Information Services contain accurate and up to date clinical/scientific information, as well as shared within all cross-functional partners in a timely manner. Staff Medical Information booths at targeted medical conferences and lead the Medical Information strategy at Local scientific congresses.Responsible for managing budget for the assigned projects. qualifications: REQUIREMENTS/PREFERENCES Education Requirement(s): Advanced degree (M.D., Ph.D, Pharm.D, M.Sc or equivalent) in a scientific discipline Skill & Competency Requirements: A minimum of 2 years' experience in pharmaceutical company or medical communication agency.Experience writing responses to scientific inquires and putting together scientific communication decks, reports and materials for educational activities.Proven ability to interpret scientific and clinical trial data and present that information in different formats for appropriate audiences. Team player who is willing to teach and bring others along the content generation journey. Ability to drive and inspire team in a matrixial environment.Experience implementing medical communication and congress programs, including omnichannel communication and digital channels/tools.Understand and interpret medical/scientific data and develop strategic messaging and knowledge of pharmaceutical standards, compliance, and regulations.Attention to detail and committed follow-through are essential attributes for this role.Strong project management skills. Travel Requirements: Ability to travel 15-25% to various domestic professional meetings, conferences, etc. - limited overnight. skills: Other, Medical Information Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).