DAWAR CONSULTING INC
51 - 200 employees
Founded 2009
⚕️ Healthcare Insurance
👥 HR Tech
☁️ SaaS
Healthcare Insurance • HR Tech • SaaS
DAWAR CONSULTING INC. is a trusted provider of workforce solutions and professional services tailored for the Medical Science industry. Specializing in Human Capital Management (HCM) and ITSM consulting, DAWAR offers expert implementation of SaaS and Cloud-based solutions from platforms like Workday and ServiceNow. Their comprehensive staffing services include global talent acquisition, recruitment process outsourcing, and staff augmentation, ensuring that they connect skilled professionals with career opportunities while enhancing organizational productivity and efficiency.
Clinical Science Program Specialist
Job not on LinkedIn
🕒 June 22
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DAWAR CONSULTING INC
51 - 200 employees
Founded 2009
⚕️ Healthcare Insurance
👥 HR Tech
☁️ SaaS
Healthcare Insurance • HR Tech • SaaS
DAWAR CONSULTING INC. is a trusted provider of workforce solutions and professional services tailored for the Medical Science industry. Specializing in Human Capital Management (HCM) and ITSM consulting, DAWAR offers expert implementation of SaaS and Cloud-based solutions from platforms like Workday and ServiceNow. Their comprehensive staffing services include global talent acquisition, recruitment process outsourcing, and staff augmentation, ensuring that they connect skilled professionals with career opportunities while enhancing organizational productivity and efficiency.
📋 Description
• Manage multiple clinical testing and lab services projects under the guidance of the Program Manager. • Develop project plans, timelines, and coordinate cross-functional activities to ensure on-time execution. • Monitor project progress, identify risks and bottlenecks, and implement solutions to maintain milestones. • Oversee sample processing workflows and ensure accurate reporting of results. • Serve as the primary liaison for pharmaceutical clients, CROs, site investigators, and internal stakeholders. • Coordinate meetings, prepare agendas, document minutes, and communicate project updates. • Track and maintain project reports and clinical study data. • Promote best practices and continuous improvement across clinical operations.
🎯 Requirements
• Bachelor’s degree required; Life Sciences preferred. • 2+ years of project coordination, clinical trial coordination, or project management experience in the CRO, diagnostics, pharmaceutical, or regulated industry. • Exposure to clinical studies and regulated documentation. • Strong organizational, communication, and collaboration skills. • Ability to manage multiple projects in a fast-paced environment.
🏖️ Benefits
• Medical • Dental • Vision • Paid Sick leave • 401K
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