Enter a job title or keyword

Clinical Science Program Specialist (100 Remote)


Job Location:

Tucson, AZ - USA

Monthly Salary: Not provided by the employer
Posted: 24 June 2026 (30+ days ago)
Application Deadline: 21 September 2026
Vacancies: 1 Vacancy

Job Summary

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:

  • Bachelors 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.




If interested please send us your updated resume at

/






Required Skills:

(clinical trial or clinical) and (project coordinator or program coordinator or project specialist or project management) and (sponsors or pharma partners)