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URGENT
Seeking a skilled Senior Clinical Trials Manager to oversee complex clinical studies globally. Drive study planning, stakeholder communication, and CRO/vendor management for on-time, quality project delivery. Requirements include GCP knowledge, stron...
Full time
Work experience placement
Paramus, NJ

Sai Krishna
Join MMS, a top CRO, crafting high-quality submissions for pharma industries globally. Seek a skilled Medical Writer to produce top-tier clinical docs, ensuring scientific accuracy and compliance. Ideal candidates boast 3-5 years of med writing exper...
Remote job
Full time
Princeton, NJ

MMS
MMS seeks a skilled Medical Writer to evaluate and interpret medical literature for study design, author clinical documents like protocols and reports, and ensure timely completion with high-quality standards. Ideal candidate has 3+ years pharma expe...
Remote job
Full time
Naperville, IL

MMS
NEW
Primary contact for Clinical project lead, supporting Life Cycle Management/Post Production risk review. Evaluate clinical data, perform gap assessments, author MDR-related documents. Develop post-market clinical plan templates, conduct literature re...
For contractors
Duluth, GA

Saviance Technologies
Lead clinically for anti-TL1A program in inflammatory diseases, expanding to immune and fibrotic. Direct multifunctional teams & oversee clinical activities such as protocol development, data review, submissions for FDA/EMA. Engage experts & regulato...
Cambridge, MA

Seeking Clinical Supervisor in Cherry Hill, NJ, offering $69k/yr. Lead Master’s-level Clinicians, provide weekly reflective sessions, ensure FBR model adherence, review referrals, coordinate with DCF, provide clinical care, submit progress reports, a...
Contract work
Local area
Immediate start
Cherry Hill, NJ

System One
Lead dermatology programs as Senior Clinical Research Director. Mentor CRDs, harmonize operational approaches, provide medical expertise, and contribute to submission dossiers. Collaborate internally and externally, ensuring quality and value in clin...
Cambridge, MA

MMS seeks an experienced Medical Writer to analyze medical literature, create clinical documents, and adhere to regulatory standards. The ideal candidate holds a scientific or medical degree, has extensive industry experience, and excels in writing f...
Remote job
Full time
Silver Spring, MD

MMS
MMS, a leading CRO, seeks an experienced Medical Writer to craft clinical development documents, ensuring scientific integrity and regulatory compliance. Ideal candidates possess 3-5 years of industry writing experience, a relevant degree, and profic...
Remote job
Full time
Franklin, TN

MMS
Lead Pfizer's Oncology Research Project Management team overseeing biologics programs, ensuring projects meet milestones. Develop standardized processes, collaborate with cross-functional teams, and strategize to advance the Oncology pipeline effecti...
Holiday work
Permanent employment
Full time
Local area
Relocation package
La Jolla, CA

Pfizer

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