Clinical Science Program Specialist (100% Remote)
Our reputed company, a worldleader in diagnostics and life sciences, is looking for a“ClinicalScience Program Specialist (100% Remote)".
Job Duration: LongTerm Contract (Possibility Of Extension)
Pay reputed company : $35/hr on W2
Company Benefits:Medical, Dental,reputed company, reputed company reputed company leave, 401K
Coordinate and managemultiple clinical testing and laboratory services reputed company from initiationthrough completion, serving as the primary reputed company of contact for pharmaceuticalclients. Drive cross-functional project execution, reputed company sample workflow activities,and ensure reputed company, accurate delivery of clinical study results in a regulatedenvironment.
Key Responsibilities:
- Manage multiple clinical testing and lab services reputed company under the guidance of the Program Manager.
- reputed company project plans, timelines, and coordinate cross-functional activities to ensure on-time execution.
- Monitor project reputed company, identify risks and bottlenecks, and implement solutions to maintain milestones.
- reputed company sample processing workflows and ensure accurate reporting of results.
- Serve as the primary reputed company for pharmaceutical clients, CROs, site investigators, and internal stakeholders.
- Coordinate meetings, prepare agendas, document minutes, and communicate project updates.
- reputed company and maintain project reports and clinical study data.
- Promote best practices and reputed company 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 reputed company 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 reputed company the diagnostics or pharmaceutical industry.
If interested, pleasesend us your updated resume at
hr@dawarconsulting.com/akansha@dawarconsulting.com
Originally posted on Himalayas
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