Clinovo Jobs in United States

Sponsor customer seeks Sr CDM Manager to work onsite at their team. · This role contributes database development data quality oversight vendor coordination to ensure accurate compliant submission-ready data.• Support design development validation clinical trial databases eCRFs; · ...

Serves as subject matter expert and has broad responsibility for the design development analysis and reporting of all clinical studies trials in accordance with the clinical development plan strategy and timelines. · ...

+We are seeking a seasoned Executive Director to Vice President–level Clinical Operations leader to build, lead, and execute the clinical operations function within a growth-stage biotechnology company. · Key responsibilities include establishing and scaling the clinical operatio ...

We are seeking a fully dedicated Chief Medical Officer to steer clinical excellence, drive innovative trial strategies, and elevate our credibility with top-tier biotech and pharmaceutical sponsors. · This is a unique opportunity to leverage your oncology expertise in a leadershi ...

This position will report to the Medical Writing Department Head and lead scientific, medical and regulatory writing activities for development projects. · Manages all clinical writing activities outlined in the Project Clinical Development Plans Reviews documents. · Createss age ...

Sponsor customer is seeking a Sr. CDM/Manager CDM for their team. · This role will contribute to database development, · data quality oversight, · and vendor coordination to ensure accurate, · compliant, · and submission-ready data. · The ideal candidate will bring strong hands-o ...

The Fractional CMO will serve as the senior clinical and medical advisor for the organization, guiding clinical strategy, trial design, regulatory direction, and external engagement. This individual must bring meaningful expertise in stroke or acute neurological indications, expe ...

Job Overview: We are seeking a Chief Medical Officer Consultant to serve as our senior clinical advisor guiding clinical strategy, trial design, regulatory direction, · and external engagement. · Clinical & Scientific Leadership: · ,<ul class= ...

The Senior Clinical Research Associate is responsible for clinical site management and monitoring activities to ensure adherence to study protocols, GCP guidelines, and applicable regulations. · ...

The Senior Clinical Research Associate is responsible for clinical site management and monitoring activities. · Perform on-site and remote monitoring visits. · Conduct source data verification. · ...

The Senior Director is responsible for supporting the development and implementation of a risk management system for risk detection, risk assessment, and risk minimization for investigational and marketed products. · ...

This role will contribute to database development, data quality oversight, and vendor coordination to ensure accurate, · compliant, and submission-ready data. · ...

A Sr. CDM/Manager CDM is sought for their team. · This role will contribute to database development, · data quality oversight, · and vendor coordination to ensure accurate, · compliant,and submission-ready data.The ideal candidate will bring strong hands-on experience · and a col ...

The key account manager promotes approved products by developing long-term relationships with ophthalmic surgeons. · This role requires interaction with customers including ophthalmic physicians nurses billing staff administrators financial personnel etc. ...

Senior Clinical Data Manager · Role Overview · The Senior Clinical Data Manager will play a critical role in database development, data quality oversight, and vendor coordination to ensure accurate, compliant, and submission-ready clinical trial data. This role requires strong h ...