Clinical Science Program Specialist (100% Remote)

dawarconsulting; Tucson (AZ); Remote; USD 41,000 - 55,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Paid Sick leave

401K

Job summary

Our client, a world leader in diagnostics and life sciences, is seeking a Clinical Science Program Specialist for a 100% remote, long-term contract role.

You will coordinate multiple clinical testing and lab services projects, develop plans, monitor progress, and serve as liaison with pharma clients and CROs, ensuring compliant, timely results.

Qualifications

• Bachelor’s degree in Life Sciences or related field.
• 2+ years coordinating clinical trials or projects in CRO/diagnostics.
• Experience with regulated documentation and PMI methods.

Responsibilities

• 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.
• 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.

Skills

Projects coordination

Cross-functional collaboration

Organizational skills

Communication skills

Multi-project management

Education

Bachelor's degree

Life Sciences background

Job 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

Company Benefits:

• Medical
• Dental
• Vision
• Paid Sick leave
• 401K

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.

Preferred Qualifications:

• 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.