Clinical Research Career Research and Resources

GlaxoSmithKline

Research - Clinical Research - Research Triangle Park, NC

Led and managed the operational conduct of numerous clinical trials from Phase I-IIB in oncology and neurology therapeutic areas. Determined appropriate resources required throughout the study lifecycle. Delineated study objectives, required resources, budget and timeline management. Collaborated with study team members with strong leadership and communication skills to deliver high quality and timely study data.

Avg. Salary: $85,000   ·    Company Rank: Not Available

GlaxoSmithKline

Research - Clinical Research - Research Triangle Park, NC

Managed the operational conduct of numerous oncology clinical trials with a major concentration in colon, breast, lung and lymphoma research. Monitored clinical study sites in addition to operational responsibilities.

Avg. Salary: $85,000   ·    Company Rank: Not Available

Burroughs Wellcome

Research - Clinical Research - Research Triangle Park, NC

Assisted clinical monitors and senior staff with all clinical research activities.

Avg. Salary: $85,000   ·    Company Rank: Not Available

Alcon Laboratories

Research - Clinical Research - Ft. Worth, TX

Lead data manager for Phase I through Phase IV clinical studies from study start up to database lock, presentations, training CDM, site and clinical personnel.

Avg. Salary: $67,500   ·    Company Rank: Not Available

University of Alabama-Birmingham

Research - Clinical Research - Birmingham, AL

Direct all phases of Phase I, II, III, and IV oncology clinical trials, including preparation of site for study initiation, design of site screening materials, development and evaluation of new research protocols, and data capturing, recording, and management. Monitor site team activities ensuring compliance with Good Clinical Practices and Federal, State, and Institutional regulatory requirements. Compassionately and patie...

Avg. Salary: $48,000   ·    Company Rank: Not Available

Crosstrees Medical

Research - Clinical Research - Boulder, CO

Monitors over 15 national clinical trial sites and 3 international sites. Writes protocols, consent forms, and protocol amendments for clinical trials. Trains study staff at various locations in how to participate in clinical trials through site qualification, initiation, and interim monitoring visits as well as at investigator and coordinator meetings. Assists in data collection and analysis. Performs close out site vi...

Avg. Salary: $53,000   ·    Company Rank: Not Available

Schulman Associates IRB

Research - Clinical Research - Cincinnati, OH

Serve as a primary operational contact for sponsors and contract research organizations (CROs) Act as the primary customer service point of contact for day to day processes and issues Monitor key processing for assigned studies Take ownership of problem resolution or service recovery efforts as necessary Coordinate specific or unique requirements with operations teams Monitor Board meeting when assigned studies or submissio...

Avg. Salary: $71,000   ·    Company Rank: Not Available

Schulman Associates IRB

Research - Clinical Research - Cincinnati, OH

Serve as manager of the IRB Coordinators Team Coordinate the workflow of the IRB Coordinators Team Facilitate the orientation and training of new hires for the IRB Coordinators Team Serve as a liaison between the Board and sponsors to address and resolve action items from Board meetings in a timely manner Manage study start-up process to assist sponsors and sites during the initial phase of IRB submission Coordinate Board ...

Avg. Salary: $71,000   ·    Company Rank: Not Available

Schulman Associates IRB

Research - Clinical Research - Cincinnati, OH

Serve as a liaison between the Board and sponsors to address and resolve action items from Board meetings in a timely manner Manage study start-up process to assist sponsors and sites during the initial phase of IRB submission Coordinate Board review of protocols and amendments Draft and edit informed consent documents based on federal regulations and Board requirements Negotiate final informed consent document between Bo...

Avg. Salary: $71,000   ·    Company Rank: Not Available

Medpace, Inc.

Research - Clinical Research - Cincinnati, OH

Participated in the site qualification, initiation, and education process Monitored on-going compliance to study protocols and site adherence to ICH/GCP Performed Pre-study Visits, Site Initiation Visits, Routine Monitoring Visits, Closeout Visits Identified potential sites for participation in new studies Collected, reviewed, and tracked regulatory documentation to ensure compliance at sites Tracked and reported progress ...

Avg. Salary: $71,000   ·    Company Rank: Not Available