Clinical Science Program Specialist (100% Remote)

Dawar Consulting, Inc.; United States; Remote; USD 40,000 - 57,000; Part time

Benefits offered by this job

Medical

Dental

Vision

Paid sick leave

401K

Job summary

Dawar Consulting, Inc. is seeking a ClinicalScience Program Specialist for a 100% remote, long-term contract.

The role focuses on coordinating multiple clinical testing and lab services projects from initiation through completion, serving as the primary contact for pharmaceutical clients and CROs. The ideal candidate has 2+ years of project coordination or clinical trial management experience in regulated environments, with strong organizational and communication skills.

Qualifications

• Bachelor’s degree required; Life Sciences preferred.
• 2+ years of project coordination, clinical trial coordination, or project management in CRO/diagnostics/pharma.
• Exposure to clinical studies and regulated documentation.

Responsibilities

• Coordinate and manage multiple clinical testing and lab services projects from initiation to completion.
• Develop project plans, timelines, and coordinate cross-functional activities to ensure on-time execution.
• Monitor progress, identify risks, 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 updates.
• Track and maintain project reports and clinical study data.
• Promote best practices and continuous improvement across clinical operations.

Skills

Project coordination

Clinical trials

Communication

Collaboration

Multi-project management

Education

Bachelor's degree in Life Sciences

Tools

PMI methodologies

Job description

Our client, a worldleader in diagnostics and life sciences, is looking for a “ClinicalScience Program Specialist (100% Remote)". Job Duration: LongTerm Contract (Possibility Of Extension) Pay Rate : $35/hr on W2 Company Benefits: Medical, Dental,Vision, Paid Sick leave, 401K Coordinate and managemultiple clinical testing and laboratory services projects from initiationthrough completion, serving as the primary point of contact for pharmaceuticalclients. Drive cross-functional project execution, oversee sample workflow activities,and ensure timely, accurate delivery of clinical study results in a regulatedenvironment.

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.

PreferredQualifications:

• 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.