Clinical Science Program Specialist (100% Remote)

Dawar Consulting; Tucson (AZ); Remote; USD 39,778 - 56,653; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

Paid Sick Leave

401K

Job summary

Dawar Consulting is seeking a Clinical Science Program Specialist for a 100% remote position based in Tucson, Arizona. This long-term contract role involves managing multiple clinical testing and laboratory services projects, driving project execution, and ensuring timely delivery of results.

The ideal candidate will hold a Bachelor’s degree in Life Sciences and possess 2+ years of experience in project coordination within the CRO or pharmaceutical industry. Familiarity with clinical studies is a plus. The company offers a competitive pay rate along with benefits including medical and dental coverage.

Qualifications

• 2+ years of project coordination, clinical trial coordination, or project management experience in the CRO or pharmaceutical industry.
• Exposure to clinical studies and regulated documentation.
• Experience with companion diagnostics (CDx) and clinical testing preferred.

Responsibilities

• Manage multiple clinical testing and laboratory services projects.
• Develop project plans and monitor project progress.
• Serve as the primary liaison for clients, overseeing workflows.

Skills

Project Coordination

Strong Organizational Skills

Communication Skills

Collaboration Skills

Ability to Manage Multiple Projects

Education

Bachelor’s degree in Life Sciences

Job description

Clinical Science Program Specialist (100% Remote)

Tucson, United States | Posted on 06/23/2026

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:

• Managemultiple clinical testing and lab services projects under the guidance ofthe Program Manager.
  
• Developproject plans, timelines, and coordinate cross-functional activities toensure on-time execution.
  
• Monitorproject progress, identify risks and bottlenecks, and implement solutionsto maintain milestones.
  
• Overseesample processing workflows and ensure accurate reporting of results.
  
• Serveas the primary liaison for pharmaceutical clients, CROs, siteinvestigators, and internal stakeholders.
  
• Coordinatemeetings, prepare agendas, document minutes, and communicate projectupdates.
  
• Trackand maintain project reports and clinical study data.
  
• Promotebest practices and continuous improvement across clinical operations.
  

Qualifications:

• Bachelor’sdegree required; Life Sciences preferred.
  
• 2+years of project coordination, clinical trial coordination, or projectmanagement experience in the CRO, diagnostics, pharmaceutical, orregulated industry.
  
• Exposureto clinical studies and regulated documentation.
  
• Strongorganizational, communication, and collaboration skills.
  
• Abilityto manage multiple projects in a fast-paced environment.
  

PreferredQualifications:

• Experiencewith companion diagnostics (CDx), clinical testing, or biosamplemanagement.
  
• Knowledgeof clinical trial management processes and PMI methodologies.
  
• Experiencewithin the diagnostics or pharmaceutical industry.
  

If interested, pleasesend us your updated resume at