The Senior Consultant will partner with life sciences clients to develop growth strategies, improve operational effectiveness, and support organizational transformation. They will manage workstreams, conduct research and analysis, and provide strategic insights to address complex business challenges.
Support the implementation, configuration, and optimization of the iTakeControl platform for clinical studies. Coordinate activities between cross-functional teams, manage device inventory, and conduct quality assurance and user acceptance testing.
The associate will manage clinical study operations from startup through closeout, including site and vendor relationships. They will also develop operational documentation, support site training, and participate in protocol design and implementation.
Manage and review clinical and ePRO data while developing data management plans and study documentation. Collaborate with cross-functional teams to support data transfers, migrations, and remote monitoring initiatives.
The Senior Director will lead a high-performing team to generate new business and expand strategic client relationships within the R&D sector. They are responsible for executing enterprise-level go-to-market strategies while maintaining disciplined pipeline management and profitable engagement scoping.
The Senior Instructional Designer will lead the design and development of engaging instructor-led and virtual learning solutions for life sciences industry professionals. This role involves collaborating with subject matter experts and stakeholders to translate business objectives into effective learning experiences.
The Scientific Director provides end-to-end strategic leadership for high-complexity accounts, overseeing publication strategies and content excellence. They are responsible for managing scientific teams, mentoring staff, and serving as the primary scientific voice to clients.
The Medical Writer will research, write, and edit various scientific deliverables including manuscripts, abstracts, and slide presentations. They will collaborate with the medical communications team to ensure the accuracy of scientific data and adherence to project deadlines.
The Account Executive supports senior team members in driving Learning and Development projects through internal processes and client interactions. Responsibilities include managing project timelines, monitoring budgets, coordinating regulatory reviews, and ensuring deliverables meet client expectations.
The Associate Director leads high-impact consulting engagements focused on pricing, market access, and commercialization strategy for pharmaceutical and biotech clients. They are responsible for managing client relationships, overseeing project delivery, and mentoring team members to ensure high-performance outcomes.
The consultant will partner with internal leadership and clients to develop and implement medical affairs strategies that drive growth and operational efficiency. They are responsible for managing workstreams, conducting in-depth research, and providing actionable insights to support client objectives.
The consultant will partner with internal leadership and clients to develop and implement medical affairs strategies that drive growth and operational efficiency. Responsibilities include managing workstreams, conducting in-depth research, and providing actionable insights to support organizational transformation.
The role involves supporting health economics and outcomes research, evidence generation, and evidence synthesis projects across various therapeutic areas. Responsibilities include designing literature reviews, interpreting complex clinical and economic data, and supervising junior colleagues on specific workstreams.
The Director of Business Development will strategically position and sell HEOR services to pharmaceutical and biotech decision-makers. Responsibilities include managing the full sales cycle, from lead generation and proposal writing to closing deals and ensuring a smooth transition to delivery teams.
The Managing Director will drive business growth by securing and leading a multi-million dollar book of business within the life sciences market access sector. They are responsible for leading high-performing delivery teams, developing innovative client solutions, and fostering a culture of excellence and strategic growth.
The Managing Director will lead business development efforts to secure a $3 million annual book of business while providing strategic advisory services to life sciences clients. They are responsible for overseeing project delivery, fostering a high-performing global team, and driving the firm's growth and scalability.
The Director is responsible for positioning and selling Value, Access, Pricing, and Evidence solutions to pharmaceutical and biotechnology clients. This role focuses on new business generation, account expansion, and managing complex, high-value strategic client relationships.
The Managing Director will lead business development efforts to secure a $3 million annual book of business while serving as a trusted advisor to life sciences clients. They are responsible for designing innovative commercial solutions, leading delivery teams, and contributing to the firm's overall strategic growth.
Lead the Japan Regulatory Operations team by owning end-to-end eCTD publishing, submission management, and regulatory information systems. Serve as a primary client contact to ensure the quality, timeliness, and compliance of major global regulatory filings.
Drive strategic account expansion and enterprise-level revenue growth by deepening relationships within high-value life sciences client organizations. Lead cross-functional sales strategies and major pursuits to unify the company's consulting, communications, and technology capabilities.
Lead strategic client relationships for accounts valued between $2M and $4M, ensuring client satisfaction and organic growth. Translate business and scientific objectives into strategic direction while overseeing the financial health and execution of medical communications projects.
Responsible for selling Medical Affairs Advisory and Medical Communications solutions to pharmaceutical and biotechnology clients. The role involves identifying new business opportunities, growing existing accounts, and collaborating with internal teams to design high-impact proposals.
The Director provides strategic leadership for high-complexity accounts, overseeing scientific communication strategies and content excellence. They are responsible for managing a team of writers and serving as the primary scientific voice for client stakeholders.
The Associate Scientific Director provides strategic leadership for medical communication accounts, overseeing content excellence and publication strategies. They manage a team of writers and serve as the primary scientific contact for client stakeholders.
Lead scientific strategy and full account ownership for medical communications, overseeing content excellence across manuscripts and congress materials. Manage a team of writers and serve as the primary scientific contact for client stakeholders.
Lead scientific strategy and ownership for one or more accounts, overseeing the creation of high-quality medical content and publication plans. Manage a team of writers and serve as the primary scientific contact for client stakeholders and clinical leads.
The Medical Writer is responsible for the development, scientific integrity, and accuracy of medical content for pharmaceutical and medical device clients. They collaborate with cross-functional teams to execute deliverables while ensuring alignment with regulatory, compliance, and client standards.
