Clinical Project Manager Jobs in California
178 California Clinical Project Manager jobs found on Monster.Jobs 1 to 20 of 178
Description: Senior Project Manager - Clinical Analytics The Clinical Analytics - Clinical Performance Measurement team focuses on provider performance measurement and reporting to support consumer transparency on health care. We work internally with different business areas to produce UnitedHealth PremiumÂ® Designation Program, which recognizes physicians that meet guidelines for providing qualit...
Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Project Manager II Job ID: 23584 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 12 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive...
Our client is seeking an Allscripts Training Analyst in Pasadena, California (CA). Under the direction of the Training Project Manager, provides support for deploying the CIS Training programs, including: staff training, defining and developing training curriculum including all course materials, reference materials, and exercises for the end-users; evaluating end user satisfaction with training; m...
Job Title: Sr. Clinical Trial Manager Position Description The Clinical Trial Manager/Sr. Clinical Trial Manager (CTM/Sr. CTM) is responsible for leading a clinical operations team to ensure the highest quality of clinical operations deliverables, effective implementation and execution of clinical trials within agreed timelines, resources and budget, and direct management of a team of Clinical Res...
please email your resume to ***** Clinical Operations Manager Long Term Contract Berkeley, CA Area MAJOR DUTIES OF POSITION: Participates in strategic discussions regarding the design of global clinical programs and in reporting the progress of clinical programs by working collaboratively with the global Core Team and sub-teams. Negotiates study timelines during project devel...
On March 12, 2014, SYNARC and BioClinica have completed the transaction to merge companies, creating a leading global provider of specialized outsourced clinical trial services. At our centers in the United States, Europe, and Asia, we provide our clients with the industry's highest quality of service across modalities and therapeutic areas. Synarc is looking for intelligent, creative and dedicate...
DUTIES: Assists in the planning and execution of clinical projects while adhering to budget, scope and schedule requirements Responsible for the execution of a suite of clinical trials from protocol design to the final clinical study report Creates and maintains clinical program timelines for study start-up, maintenance and close-out Attend Clinical Development Subteam meetings and inform members...
This is an exciting opportunity to join an emerging biotechnology company focused on developing therapeutics for patients with rare diseases. The ideal candidate is a data manager who thrives in a fast paced environment and is looking for a unique opportunity to develop a multi-dimensional and well-rounded Data Management skill set with possible exposure to database development, SOP development an...
Job Details The Clinical Program Manager will provide clinical support to the ACO Program collaborations with a focus on Health Information Technology (HIT) initiatives under the direction of the ACO Medical Director. This position located at Blue Shield of California offices in San Francisco and will require statewide travel to Northern and Southern California locations. Responsibilities: • Respo...
Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Regulatory Affairs Senior Manager (Biosimilars) Job ID: 23485 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 18 Month Contract – Possible temp to hire Pay...
The Clinical Trial Manager is responsible for: Activities ensuring high quality deliverables are within budget and timelines. Support cross-functional Study Team within Clinical Operations with minimal oversight from the CTM and/or CPL. Clinical Operations deliverables to achieve study objectives and milestones within timelines and budget. Responsible for vendor selection and management including...
Clinical Program Manager: One of Real Staffing Group's clients is seeking a Clinical Program Manager who will ensure that assigned clinical trials are executed on time, on budget, and in compliance with applicable guidelines and regulations by providing leadership to a multi-functional study team. Responsibilities: Executes clinical trials by directing a multi-functional study team. Ensures that t...
Clinical Supply Manager - Project Manager Redwood City, CA. Minimum Requirements: Bachelor’s Degree required, preferably in physical science, math, engineering, or pharmacy. 3 - 5+ years total experience in the Pharmaceutical Industry. Job Responsibilities: Responsible for the project management of key Clinical Supply Chain activities at the protocol level for Phase I – IV clinical trials of varyi...
Company Confidential South San Francisco, CA, 94080
Purpose: The Research and Early Development contract Clinical Trial Manager (cCTM) provides support and/or leadership to one or more global Study Teams within an early development program(s) (i.e. phase I and II trials). The cCTM is accountable for activities ensuring high quality deliverables are within budget and timelines. Primary Accountabilities and Responsibilities: • Support cross-functiona...
Must Apply Here to be Considered: http://jobs.ucsd.edu/bulletin/job.aspx?cat=search&sortby=rank&jobnum_in=70307&search=70307 DESCRIPTION Under direction, incumbent will manage the clinical applications team with broad oversight of clinical applications used in all ambulatory practices, including Medical Center, Medical Group, and Health Sciences at UC San Diego. Responsible for the complete life c...
Primary Responsibilities: Responsible for conducting clinical programs consistent with applicable regulations, guidelines, and policies. Ensures study adherence to ICH/GCP and SOPs Research, prepare, and revise the study protocol, Monitoring Plans, Informed Consent/Assent Forms, Case Report Forms, etc., in consultation with the cross-functional project team, investigators, data management, and bio...
Responsibilities Responsible for conducting clinical programs consistent with applicable regulations, guidelines, and policies. Ensures study adherence to ICH/GCP and SOPs Research, prepare, and revise the study protocol, Monitoring Plans, Informed Consent/Assent Forms, Case Report Forms, etc., in consultation with the cross-functional project team, investigators, data management, and biostatistic...
Specific responsibilities: Develop and manage study timelines, milestones and budgets in collaboration with trial team members. Develop study protocols with guidance from Medical Monitor. Develop case report forms, informed consent forms and other study-related documents. Selection and qualification of investigational sites. Participate in selection of, management and oversight of CROs and other v...
Job Description: Requires minimal supervision to manage various activities associated with multiple clinical studies in accordance with designated project assignments. Uses thorough knowledge of FDA regulations and ICH guidelines to ensure compliance with both during clinical trial conduct. Has had experience as clinical operations co-lead/lead on a significant Phase II or Phase III program. Indep...
Duties: Requires minimal supervision to manage various activities associated with multiple clinical studies in accordance with designated project assignments. Uses thorough knowledge of FDA regulations and ICH guidelines to ensure compliance with both during clinical trial conduct. Has had experience as clinical operations co-lead/lead on a significant Phase II or Phase III program. Independently...
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Healthcare Career Tools
Clinical Affairs Associate Manager
$41,600.00 - $165,000.00
Typical Salary for Clinical Affairs Associate Manager in California
Source: Monster.com Careerbenchmarking Tool
Education / Training
Source: Monster.com Careerbenchmarking Tool
Clinical Affairs Associate Manager
Provides patients for clinical trials by developing recruitment strategies; utilizing media; retaining patient recruitment specialists; integrating clinical trials into operations plans.
Rate of Growth
Size of Industry in 2006:
Source: Bureau of Labor Statistics, May 2006
Administrative Writing Skills
Attention to Detail
Clinical Lab Testing
Controls costs by forecasting requirements; preparing an annual budget; scheduling expenditures; analyzing variances; initiating corrective actions; implementing cost-saving actions.
Identifies strategies necessary to impact patient accrual by coordinating interdepartmental recruitment strategy implementation; traveling to clinical trial sites; presenting potential recruitment strategies; utilizing media, networks, direct advertising; engaging vendors specialized in patient recruitment.
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