Dawar Consulting, Inc.

Role Description Our client, a world leader in biotechnology and gene therapy, is looking for a Clinical Labeling Operations Specialist (100% Remote). Job Duration: Long Term Contract (Possibility Of Extension) Pay Rate: $56.79/hr on W2 The Labeling Operations Specialist coordinates the implementation of new clinical labeling and labeling updates across various departments worldwide. This role ensures label content is accurately transferred, mapped, reviewed, and implemented in accordance with source documents, FDA requirements, cGMP standards, and applicable regulatory guidance. - Coordinate global clinical labeling implementation with Regulatory Affairs, Quality, Supply Chain, PMs, and packaging sites. - Create and map label content within Bartender and develop Business Continuity Labels. - Review final product label content and mapping for accuracy and alignment with source documents. - Partner with Regulatory Affairs to obtain approved text, manage timelines, and ensure requirements are met. - Lead operational excellence and process improvement projects. - Author and update SOPs, guidelines, and work instructions. - Support labeling updates and collaborate cross-functionally to meet departmental objectives. Qualifications - Bachelor’s degree with 6+ years of relevant experience, or Master’s degree with 4+ years of relevant experience. - Experience in the pharmaceutical or other regulated industry. - Experience with clinical or commercial supply chain operations. - Familiarity with pharmaceutical artwork and labeling production. - Knowledge of FDA regulations, cGMP standards, and regulatory guidance. - Strong project coordination, communication, technical writing, and interpersonal skills. - Proficiency with Microsoft Office. Requirements - Preferred: Experience with Bartender software and label content mapping. Benefits - Medical - Paid Sick leave - 401K If interested, please send us your updated resume at hr@dawarconsulting.com / akansha@dawarconsulting.com

Role Description Our client, a world leader in biotechnology and gene therapy, is looking for an “US Medical Contact Center Oversight and Strategy Lead (100% Remote)”. Job Duration: Long Term Contract (Possibility Of Extension) Pay Rate: $96/hr on W2 Seeking an experienced professional to oversee the US Medical Contact Center vendor and drive operational excellence across Medical Information, Adverse Event Intake, Trial Information Support, and Compassionate Use programs. This role is responsible for vendor governance, performance management, compliance, financial oversight, and leading digital transformation initiatives, including AI-enabled customer service solutions. - Oversee day-to-day operations and governance of the US Medical Contact Center vendor. - Monitor vendor performance, KPIs, SLAs, and drive continuous process improvements. - Ensure compliance with GCP, GVP, regulatory requirements, and audit readiness. - Manage budgets, forecasting, resource planning, SOWs, and operational governance. - Partner with internal stakeholders to align contact center strategy with evolving business needs. - Lead digital transformation initiatives, including AI, automation, CRM optimization, and multi-channel engagement. - Analyze operational metrics and implement strategies to enhance customer experience and operational efficiency. Qualifications - Bachelor's degree in Business, Life Sciences, Healthcare, or a related field (Master's/MBA preferred). - Proven experience managing or overseeing a Medical Contact Center within the pharmaceutical industry. - Strong vendor management, stakeholder engagement, and operational leadership experience. - Knowledge of GCP, GVP, pharmacovigilance, and regulatory compliance. - Experience with CRM platforms, performance analytics, budgeting, and service governance. - Excellent communication, project management, and continuous improvement skills. Benefits - Medical - Dental - Vision - Paid Sick leave - 401K If interested, please send us your updated resume at hr@dawarconsulting.com / akansha@dawarconsulting.com

Role Description In this role, you will provide strategic regulatory guidance for U.S. commercial pharmaceutical products. You will lead Promotional Review Committees (PRCs), review and approve advertising and promotional materials, and partner closely with Marketing, Medical Affairs, Legal, and Compliance to ensure FDA‑compliant communications. This position offers the opportunity to shape commercial regulatory strategy for innovative therapies in a fast‑paced biotech environment. - Lead Promotional Review Committee (PRC) meetings - Review and approve promotional and marketing materials - Provide regulatory guidance on advertising and promotional claims - Partner with Marketing, Medical, Legal, and Compliance teams - Support FDA communications and Form 2253 submissions - Ensure compliance with FDA regulations and healthcare industry guidelines Qualifications - Bachelor's degree required; advanced degree (PharmD, PhD, JD, MBA, MS) preferred - 7+ years of Regulatory Affairs, Commercial Regulatory, Compliance, or Advertising & Promotion experience in the biotech/pharmaceutical industry - Strong knowledge of FDA advertising & promotion regulations, promotional review, and healthcare compliance - Experience leading cross-functional teams and Promotional Review Committees (PRCs) - Excellent communication, stakeholder management, and project leadership skills Requirements - Commercial Regulatory Affairs - Advertising & Promotion (Ad/Promo) - Promotional Review Committee (PRC) - FDA Form 2253 - Medical, Legal, Regulatory (MLR) review - Product launch support Benefits - Medical - Dental - Vision - Paid Sick Leave - 401K

Role Description Our client, a world leader in diagnostics and life sciences, is looking for a “Clinical Science Program Specialist (100% Remote)”. Job Duration: Long Term Contract (Possibility Of Extension) Pay Rate: $35/hr on W2 Coordinate and manage multiple clinical testing and laboratory services projects from initiation through completion, serving as the primary point of contact for pharmaceutical clients. Drive cross-functional project execution, oversee sample workflow activities, and ensure timely, accurate delivery of clinical study results in a regulated environment. Key Responsibilities: - 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. Qualifications - 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. Requirements - Experience with companion diagnostics (CDx), clinical testing, or biosample management. - Knowledge of clinical trial management processes and PMI methodologies. - Experience within the diagnostics or pharmaceutical industry. Benefits - Medical - Dental - Vision - Paid Sick leave - 401K Company Description For more information, please send us your updated resume at hr@dawarconsulting.com/akansha@dawarconsulting.com.

Role Description This is a remote position. Our client, a world leader in biotechnology and life sciences, is seeking a "Data Visualization & Power BI Consultant (Fully Remote)". Duration: Long-Term Contract (Possibility Of Further Extension) Pay Rate: $80-$87/hr on W2 You will be partnering with enterprise teams to design, build, and enhance executive-level dashboards supporting AI and business performance. This role blends hands-on Power BI development with stakeholder engagement to create scalable, intuitive reporting experiences. Key Responsibilities: - Build Power BI dashboards from structured/semi-structured data - Develop scalable data models, DAX, Power Query, and optimized visuals - Iterate quickly based on stakeholder feedback - Define KPIs, metrics, and dashboard narratives - Create reusable templates, standards, and governance practices Qualifications - 5+ years Power BI dashboard development for business/executive audiences - Strong skills in data modeling, DAX, Power Query, and performance tuning - Experience designing tiered/role-based reporting and drill-through navigation - Ability to translate business questions into clear KPIs and insights - Experience with structured/semi-structured data (Excel, enterprise systems) - Strong stakeholder engagement; able to work independently in fast-paced environments - Experience with AI, transformation, or enterprise reporting preferred Benefits - Medical - Dental - Vision - Paid Sick Leave - 401K Company Description

Role Description This is a remote position for a Staff Pathologist (MD) who has experience diagnosing cancer in any capacity. Position will require a minimum of 20 hours a week (M-F, MST business hours) and up to 40 hours a week. Any domestic timezone is acceptable. - Perform diagnostic pathology analysis to assist in the development of Artificial Intelligence (AI) algorithms for quantitative image analysis - Ensure compliance with laboratory and medical regulations - Collaborate with medical teams on case reviews - Support research and clinical trials through pathology insights - Contribute to quality control and assurance processes Qualifications - Strong background in surgical pathology - Experience in IHC-supervised annotation for tumor identification Requirements - Surgical pathology fellowship trained (Preferred) - Board certification in anatomic pathology required Benefits - Medical - Dental - Vision - Paid Sick leave - 401K

This is a remote position. Our client, a world leader in biotechnology and life sciences, is looking for a “Medical Scientific Liaison (Remote - West Coast)". Job Duration: Long Term Contract (Possibility Of Extension) Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K Summary: In this role, you will support the upcoming launch of innovative blood-based biomarkers for Alzheimer’s disease. This role will focus on engaging and educating key opinion leaders (KOLs), neurologists, and healthcare professionals across assigned territories. Key Responsibilities: - Educate healthcare providers on Alzheimer’s diagnostics and biomarkers - Build and maintain relationships with KOLs and medical stakeholders - Gather and share insights to support strategy and product development - Present clinical and scientific content at meetings and conferences - Support scientific events, webinars, and product launches Qualifications: - Advanced degree (PhD, MD, PharmD, MSN, BSN) + 3–5 years relevant experience - Strong knowledge of neurology; Alzheimer’s experience preferred - Excellent communication and relationship-building skills - Prior MSL or diagnostic industry experience is a plus If interested, please send us your updated resume at hr@dawarconsulting.com/lakshmi@dawarconsulting.com .

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description The Clinical Operations Lead supports the execution and delivery of global clinical trials within a cross-functional, matrixed clinical development organization. This role collaborates with global teams to drive operational activities that support study delivery, improve clinical trial processes, and enhance patient, investigator, and site experiences. - Support operational execution of clinical trials and development programs across disease areas. - Provide operational and strategic input to cross-functional study teams. - Collaborate with global stakeholders to support study management, process improvements, and clinical operations initiatives. - Ensure compliance with ICH, GCP, and regulatory guidelines and maintain high standards of data integrity. - Partner with investigators and clinical sites to strengthen relationships and improve trial delivery. - Contribute to innovation, digital adoption, and continuous improvement initiatives within clinical operations. - Support global and local initiatives aligned with clinical development priorities. Qualifications - 2–5 years of experience in clinical operations, drug development, or related field. - Knowledge of clinical trial processes and regulatory guidelines (ICH/GCP). - Strong organizational, problem-solving, and communication skills. - Ability to collaborate across cross-functional and global teams in a dynamic environment. - Experience supporting clinical studies, enabling projects, or operational initiatives preferred. Requirements - Job Duration: Long Term Contract (Possibility Of Extension) - Pay Rate: $81/hr on W2 DOE Benefits - Medical - Dental - Vision - Paid Sick leave - 401K

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description Our client, a world leader in biotechnology and life sciences, is looking for an A/R Contracts Coordinator (100% Remote – US Based only). Job Duration: Long Term Contract (Possibility Of Extension) Pay Rate: $40/hr on W2 This role supports, monitors, and tracks contract milestones, payment triggers, and the resulting billings to Pharma partners across the Pathology customer areas. Responsibilities include: - Providing support for financial oversight for revenue forecasting and analysis. - Assisting the subject matter expert to develop accurate revenue and financial dashboards to drive insights, identify gaps, and compare contract terms across the portfolio to improve costs and performance. - Helping automate and drive towards effective process solutions. - Working on aged invoices in this A/R driven role. - Utilizing hands-on advanced MS Excel experience. Additional skills include: - Providing contract term input for tracking support and invoicing recordation for actual and forecast activity. - Offering tool support and necessary inputs for business processes involving the PHCS lifecycle and Pharma initiatives. - Supporting local Change Management processes related to contract management. - Delivering data and insights both verbally and in writing, involving external stakeholders where applicable. - Updating departmental systems with current and accurate information. - Playing a supporting role in developing, recommending, implementing, and providing standardized and ad hoc contract management tools. - Soliciting internal and external business partner/stakeholder input to ensure reporting meets stakeholder needs and objectives. - Working closely with cross-functional stakeholders to develop and implement appropriate metrics. Qualifications - Advanced MS Excel experience. Requirements - Hands-on experience with A/R processes. - Ability to work with cross-functional teams. Benefits - Medical - Dental - Vision - Paid Sick Leave - 401K Company Description Our client is a world leader in biotechnology and life sciences.

This is a remote position. Our client, a world leader in life sciences and biotechnology, is looking for a “Graphic Designer (Fully Remote). The role focuses on formatting, updating, and managing technical documents using Adobe InDesign and structured templates. Job Duration: Long Term Contract (Possibility Of Extension) Pay Rate: $32 - $35/hr on W2 Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K Key Responsibilities - Create and update interpretation guides and product documentation using Adobe InDesign. - Format and revise documents based on feedback from regulatory, quality, and project teams. - Ensure documents follow corporate templates and regulatory requirements. - Review documents for accuracy, formatting consistency, and completeness. - Manage multiple document updates under tight deadlines. - Support method sheet preparation using Microsoft Word templates. Required Qualifications - Bachelor’s in Graphic Design, Communication Design, Technical Communication, or related field. - 3+ years in graphic design or technical documentation. - Strong hands‑on experience with Adobe InDesign. - Experience with structured templates and large document formatting. Preferred - Experience in diagnostics, medical devices, pharma, or life sciences. - Familiarity with regulatory documentation, version control, and cross‑functional workflows If interested, please send us your updated resume at hr@dawarconsulting.com/lakshmi@dawarconsulting.com