Urgent requirement for one of the our top client located in “Cambridge, MA”. Please contact me at your earliest convenience, along with job No. COM_51607 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Responsibilities: Assists in defining protocol(s) and develops informed consent forms, patient instruction guides, and reviews draft case report forms. Serves as a liaison between company and contract research organizations, core laboratories, field sites, investigators, study coordinators, physicians and staff members ..... (continued)

Urgent requirement for one of the our top client located in “CA”. Please contact me at your earliest convenience, along with job No. RTM_52207 to xxxxxx.xxxxxx@xxxxxxxxx.xxx The Regional Clinical Trial Manager is responsible for ensuring that Company clinical research studies are conducted at quality, high performing sites, in accordance with state and federal regulations, ICH GCP guidelines, and Company SOPs. The RTM will accomplish this primarily by ensuring sites are properly selected, and that high ..... (continued)

Urgent requirement for one of the our top client located in “ Franklin Lakes, NJ ”. Please contact me at your earliest convenience, along with job No. CTPM_6107 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Description: The Therapeutic Glaucoma Initiative Trials Program Manager will be responsible for providing program facilitation and management support to the Clinical Program Leader and research teams planning and executing a multiple study clinical program relating to a major ophthalmologic medical device program. ..... (continued)

Urgent requirement for one of the our top client located in “Newark, NJ”. Please contact me at your earliest convenience, along with job No. CDM_62007 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Job Description: Responsible for the data management function and team within a therapeutic area Participation on teams in support of project goals and objectives. Responsible for query generation and resolution process. Participation in development of DM SOP's, and to supervise direct reports and conduct performance ..... (continued)

Urgent requirement for one of our top clients located in “Mountain View, CA”. Please contact me at your earliest convenience, along with job No. SCR_110307 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Description: Monitor clinical trials, study sites, and clinical data. Ensure compliance with protocol and overall clinical objectives and GCP. Provide project support to clinical programs with minimum supervision. Manage clinical study sites including study site start up and close-out. Ensure study sites follow company ..... (continued)

Urgent requirement for one of our top clients located in “Irvine, CA”. Please contact me at your earliest convenience, along with job No. CTM_112307 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Job Description: Responsible for managing the clinical project team for one or more clinical protocols. Functions as an expert resource for clinical trial monitoring activities. Proposes staffing for new and/or existing projects. Responsible for managing clinical studies in accordance with Company’s SOPs, GCPs, FDA and ICH ..... (continued)

Urgent requirement for one of our top clients located in “Mountain View, CA ”. Please contact me at your earliest convenience, along with job No. SCRA_113007 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Description: Monitor clinical trials, study sites, and clinical data. Ensure compliance with protocol and overall clinical objectives and GCP. Provide project support to clinical programs with minimum supervision. Interfaces with all project/clinical groups and off-site personnel as needed in support of project and ..... (continued)

Urgent requirement for one of our top clients located in “Northridge, CA”. Please contact me at your earliest convenience, along with job No. SCMM_022708 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Description: The Clinical Research Manager of Field Operations is responsible for overseeing and managing all US Clinical Research activities related to active and impending active clinical studies as well as managing the daily field operations associated with these studies. This position must be able to independently ..... (continued)

If you have a moment, I would appreciate your help in our search for uniquely qualified and specialized professionals. Please take a look and forward this open job on to anyone you think would be interested in the position, or anyone else who could help me find a great candidate. If you are applying yourself then please don’t hesitate to forward your updated resume, availability and your hourly/salary expectations to xxxxxx.xxxxxx@xxxxxxxxx.xxx ASAP since we have multiple immediate requirements. Thanks ..... (continued)

If you have a moment, I would appreciate your help in our search for uniquely qualified and specialized professionals. Please take a look and forward this open job on to anyone you think would be interested in the position, or anyone else who could help me find a great candidate. If you are applying yourself then please don’t hesitate to forward your updated resume, availability and your hourly/salary expectations to xxxxxx.xxxxxx@xxxxxxxxx.xxx ASAP since we have multiple immediate requirements. Thanks ..... (continued)

Urgent requirement for one of our top clients located in “Palo Alto, CA”. Please contact me at your earliest convenience, along with job No. SCRA_50808 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Description: "MUST HAVE IN-HOUSE CRA INDUSTRY EXPERIENCE" Protocol development and writing, planning, study implementation and execution, conduct/oversight, clinical study monitoring and management, study budgets, CRO/vendor management and reporting. The candidate in this position may act as the Lead CRA/Clinical Project ..... (continued)

Urgent requirement for one of our top clients located in “SSF,CA”. Please contact me at your earliest convenience, along with job No. CTM_51408 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Description: The Clinical Trial Manager II is accountable for the day-to-day operations of 1-4 clinical trials commensurate with complexity, including trial start-up, conduct, and close-out activities. Leads the Protocol Execution Team (PET) to ensure that trial timelines, costs, and quality metrics are met. Ensures accuracy and ..... (continued)

Urgent requirement for one of our top clients located in “Hayward, CA”. Please contact me at your earliest convenience, along with job No. SCRA_51408 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Job Description: Responsible for the oversight and management of in-house Ph I-III clinical trials following GCP. Responsibilities as follows - serves as the project manager for selected projects; primary contact for study site personnel. Conducts project specific CRA training, as requested. Study Monitoring-Regulatory ..... (continued)

This is an excellent opportunity to be a part of a growing team and work in a progressive environment, Please contact me at your earliest convenience. Urgent requirement for one of our top clients located in “NewYork City, NY”. Please contact me at your earliest convenience, along with job No. RCRA_52408 to xxxxx.xxxxx@xxxxxxxxxxxxxxx.xxx Description: Demonstrate superior communication and organizational skills in addition to the technical skills required for overseeing clinical studies. Recognize the ..... (continued)

Urgent requirement for one of our top clients located in “Branchburg, NJ”. Please contact me at your earliest convenience, along with job No. CRA_53008 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Description: Under general supervision, monitors one or more clinical oncology investigations, including initiating and closing investigational centers and collecting, processing, and reviewing case report forms. Under general supervision, assists with the overall planning, development, and data management of one or more ..... (continued)

I would like to put forth for your consideration, please take a look and forward this open job on to anyone you think would be interested in the position, or anyone else who could help me find a great candidate. If you are applying yourself then please don’t hesitate to forward your updated resume, availability and your hourly/salary expectations to xxxxxx.xxxxxx@xxxxxxxxx.xxx ASAP since we have multiple immediate requirements. Thanks for your help! Anitha Maturi Company: Makro Technologies, Inc. Job ..... (continued)

Urgent requirement for one of our top clients located in “Fremont, CA”. Please contact me at your earliest convenience, along with job No. CPM_62008 to xxxxxx.xxxxxx@xxxxxxxxx.xxx The Clinical Project manager will provide project management and leadership on the planning, preparation and execution of one (or more) high quality clinical project(s). Lead the Neurovascular clinical project team members toward completion of deliverables in a timely fashion within an agreed project timeline. Internally ..... (continued)

This is an excellent opportunity to be a part of a growing team and work in a progressive environment, Please contact me at your earliest convenience. Urgent requirement for one of our top clients located in “Monmouth Junction, NJ”. Please contact me at your earliest convenience, along with job No. MMA_81308 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Description: Manage preparation and compilation of regulatory filings, including Investigational Device Exemptions, Clinical Trial Authorization requests to Competent ..... (continued)