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This virtual position will provide remote work from home, traveling as needed to monitor and manage site activity for SOPs. Eligible candidates will have a degree related to pharmacy or biology, plus a background in clinical trials. Freelance.

Full-time opportunity with some telecommuting. Verify procedures, ensure data integrity, prepare reports, negotiate budgets, and manage projects. Must have a minimum of 4 years of clinical monitoring experience.

Full-time opportunity with some telecommuting. Will be responsible for site monitoring and clinical close-out activities. Must have a university degree in an allied health area and a minimum of 2 years of clinical monitoring experience.

Short-term contract opportunity. Will serve as a study contact, develop protocols, monitor activities, and perform site qualification and close out tasks. Must have a bachelor’s degree and 3-5 years of experience.

Responsibilities include providing input for capacity planning, resolving site operational issues, handling people and resource management, and attending local investigator meetings. 2+ yrs of experience is required. Work at home with some travel.

Responsible for completing project activities and perform investigator activities for site management. Fluent Spanish and English speaking skills and a Bachelor’s degree in a health-related field is needed. Home-based job w/travel to Puerto Rico.

Needs a bachelor’s degree and has two year’s monitoring experience for this full-time, remote role. Monitor the progress of clinical studies on site or remotely, ensure that trials are conducted, recorded and reported in accordance with protocol.

On investigative sites or remotely, observe clinical research process and recording, ensuring protocol compliance. Requires 5+ yrs’ experience in clinical monitoring and a bachelor’s degree or equivalent experience. Telecommute position.

Full-time, remote job. Needs a bachelor’s degree and five years’ clinical monitoring experience. Conducts monitoring to confirm subject safety, describes and demonstrates the principals of IP accountability and identifies scientific misconduct.

Full-time, remote study management associate will implement studies, monitor and maintain compliance, manage project responsibilities, coordinate meetings, generate training needs. Two+ years’ similar clinical research focused experience a must.