Dawar Consulting, Inc. Verified

Clinical Science Program Specialist (100% Remote)

RemoteRemoteContract$35–$35 /hrPosted 1 month agoHidden Gem · Himalayas

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Required skills

clinical testing
laboratory services
project management
regulated environment
project plans
timelines
cross-functional activities
sample processing
reporting
pharmaceutical clients

Nice to have

companion diagnostics
CDx
biosample management
clinical trial management processes
PMI methodologies
diagnostics industry

Role summary

A world leader in diagnostics and life sciences seeks a remote Clinical Science Program Specialist for a long-term contract. This role involves managing multiple clinical testing and laboratory services projects from initiation to completion, serving as the primary client contact. Responsibilities include developing project plans, coordinating cross-functional teams, overseeing sample workflows, ensuring accurate results reporting in a regulated environment, and liaising with clients, CROs, and internal stakeholders. The ideal candidate has a Bachelor's degree in Life Sciences, 2+ years of project coordination or management experience in a regulated industry, and strong organizational and communication skills.

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.

If interested, pleasesend us your updated resume at

Originally posted on Himalayas

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