Associate Director managing clinical research sales initiatives and driving business growth strategy. Leading relationships with pharmaceutical, biotech, and CRO partners for a clinical research site management organization.
Responsibilities
Identify, develop, and secure new business opportunities with pharmaceutical companies, biotech firms, and CROs to place clinical trials at our managed research sites.
Build and maintain long-term relationships with key industry stakeholders, including sponsors, CROs, and investigator sites.
Lead the negotiation of budgets, and support with negotiation of contracts, master service agreements (MSAs), and clinical trial agreements to maximise revenue and profitability.
Maintain a strong pipeline of potential clinical trial opportunities and ensure timely follow-up to drive conversions.
Prepare written presentations, reports and proposals, including but not limited to formal requests for quotations, bids and tenders.
Prepare key account plans and present to the Board upon request.
Represent the organisation at industry conferences, networking events, and client meetings to enhance visibility and credibility.
Collaborate with cross-functional teams, including operations, finance, and regulatory, to ensure seamless trial execution and client satisfaction.
Ensure Salesforce is utilised to its full potential, using it as your day-to-day sales management and customer management tool.
Monitor industry trends, competitor activities, and regulatory changes to identify opportunities for business growth.
Contribute to the development and implementation of strategic business plans and clinical research specific projects that align with company objectives.
Provide reports on pipeline, revenue forecasts, and market insights.
Work closely with clinical operations to ensure site readiness, feasibility assessments, and efficient study start-up processes.
Partner with marketing to develop effective outreach campaigns and promotional materials to support business development efforts.
Serve as a key liaison between sponsors and internal teams to address client concerns and ensure superior service delivery.
Requirements
5-7 years of business development experience in a clinical research environment (CRO, SMO, or similar organization).
Strong understanding of clinical trial operations, site management, and regulatory requirements.
Proven track record of successfully securing and managing clinical trial contracts.
Demonstrated ability to build and maintain relationships with key industry stakeholders.
Bachelor's degree in life sciences, business, or a related field (advanced degree preferred).
Benefits
Bank holidays, plus 25 days annual leave, increasing to 28 after 5 years
Buy & Sell Holidays
Enhanced Maternity and Paternity Leave
1 Occasion Day each year; this could be your child’s first day of school, their nativity play, or your own birthday – the choice is yours!
Healthshield
Cycle to Work Scheme
Tech Scheme
Electric Car Scheme
Subsidised company events and gatherings
A gift for your birthday
Well being support from our qualified Mental Health First Aiders, as well as via our health scheme
Clinical Trial Manager overseeing clinical studies with a focus on Atopic Dermatitis. Ensuring compliance with ICH GCP and delivering results within contractual timelines.
Clinical Research Project Manager managing clinical trials involving radiation therapy at the Perelman School of Medicine. Ensuring adherence to protocols and supporting operational activities within the team.
Clinical Research Coordinator managing radiation oncology trials at the University of Pennsylvania. Ensuring compliance with study protocols and coordinating patient enrollment and data collection.
Clinical Research Coordinator managing investigator - initiated and sponsored clinical trials in Radiation Oncology. Ensuring compliance with study protocols and supporting patient enrollment and data collection.
Clinical Research Coordinator at Penn's Balderston lab focused on neuroscience of fear and anxiety. Involves human neuroimaging research, collaboration, and study coordination responsibilities.
Clinical Trial Nurse conducting in - home visits for clinical research at IQVIA. Supporting innovative therapies and gaining hands - on research experience with flexible scheduling.
Clinical Trial Manager at ICON managing trial operations, ensuring high - quality outcomes and compliance with trial protocols for clinical development in Beijing and Shanghai.
Clinical Research Coordinator overseeing research studies at Florida Cancer Specialists. Responsible for implementation and management of clinical trials under medical supervision.
Senior Clinical Trial Manager at Climb Bio leading end - to - end execution of Phase 1 - 3 clinical studies. Critical role in clinical operations and study management with a focus on quality and compliance.
Senior Clinical Researcher collaborating globally to design and evaluate digital health investigations. Engaging in statistical analysis and contributing to product development for cognitive health.