Top 60 clinical trial manager Jobs in mountain view ca

SCI-CTO Study Start-UP Project Manager (Hybrid)
Stanford University —Stanford, CA
- $86,248 - $100,158 a year
- Extended hours
- HIPAA
- Mid-level
- Bachelor's degree
Clinical Data Manager - II
Apollo Professional Solutions, Inc. —South San Francisco, CA
- $78 - $85 an hour
- Contract
- Hybrid work
- 5 years
- Office
- Continuous improvement
- Dental insurance
- 401(k)
Quick Apply
2d
Global Clinical Trial Leader
Tailored Management —South San Francisco, CA
- $59.89 - $87.73 an hour
- Contract
- Hybrid work
- Office
- 8 years
- Analysis skills
- Health insurance
- Dental insurance
Quick Apply
23h
Clinical Research Operations Program Manager
Google —Mountain View, CA
- $132,000 - $190,000 a year
- Full-time
- Mid-level
- Office
- SQL
- Paid holidays
- Disability insurance
1d
Clinical Research Manager
Stanford University —Stanford, CA
- $124,521 - $153,615 a year
- Extended hours
- 5 years
- HIPAA
- Master's degree
Clinical Trial Manager (CTM)
Corcept Therapeutics —Redwood City, CA
- $156,600 - $184,300 a year
- Hybrid work
- Nursing
- 6 years
- Bachelor of Science
Project Manager
Stanford University —Stanford, CA
- $109,826 - $123,774 a year
- Extended hours
- HIPAA
- Mid-level
- Bachelor's degree
Clinical Data Manager
Ceribell, Inc —Mountain View, CA
- $190,000 - $200,000 a year
- Email
- 5 years
- Bachelor's degree
- Continuous improvement
- Employee stock purchase plan
- Paid holidays
Quick Apply
10d
Sr. Clinical Study Manager
Intuitive Surgical —Sunnyvale, CA
- $128,900 - $218,300 a year
- Day shift
- Remote
- Surgery
- 5 years
- Bachelor's degree
Senior Clinical Trial Manager (Sr CTM)
Corcept Therapeutics —Redwood City, CA
- $170,500 - $200,700 a year
- Hybrid work
- Nursing
- Bachelor of Science
- Office
Senior Clinical Trial Manager - Job ID: 1955
Ascendis Pharma —Palo Alto, CA
- $160,000 - $170,000 a year
- Full-time
- Remote
- 7 years
- Microsoft Excel
- Microsoft Outlook
- Paid parental leave
- Health savings account
Quick Apply
Clinical Data Manager - T45 Labs
T45 Labs —Santa Clara, CA
- $117,000 - $159,000 a year
- Email
- Computer Science
- Office
- Analysis skills
Quick Apply
Clinical Trial Manager
Summit Therapeutics —Palo Alto, CA
- $140,000 - $150,000 a year
- Nursing
- 5 years
- Bachelor's degree
Senior Clinical Study Manager
Veranex, Inc. —San Jose, CA
- $125,600 - $179,630 a year
- Full-time
- 5 years
- Bachelor's degree
- Contracts
Quick Apply
8d
Clinical Trials Manager, Early Phase Oncology (Office Based)
Gilead Sciences —Foster City, CA
- $133,195 - $189,640 a year
- Full-time
- Mid-level
- Office
- Master's degree
- Health insurance
- Dental insurance
4d
Senior Clinical Study Manager
Intuitive Surgical —Sunnyvale, CA
- $128,900 - $218,300 a year
- Day shift
- Surgery
- 5 years
- Bachelor's degree
Interior Design Project Manager
Stanford Health Care —Palo Alto, CA
- $62.75 - $83.16 an hour
- Online Application
- Hybrid work
- Microsoft Excel
- Analysis skills
- Bachelor's degree
Payer Healthcare Data Scientist, Manager
PRICE WATERHOUSE COOPERS —Silicon Valley, CA
- $99,000 - $232,000 a year
- 6 years
- Computer Science
- Master's degree
- Paid holidays
- Health insurance
Clinical Project Manager - Pleasanton, CA
Calyxo —Pleasanton, CA
- $140,000 - $150,000 a year
- 7 years
- Up to 50% travel
- Bachelor of Science
- Health insurance
- 401(k)
Quick Apply
Clinical Trial Manager
Iovance Biotherapeutics —San Carlos, CA
- $145,000 - $165,000 a year
- Bachelor's degree
- 1 year
- Senior level
4d

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SCI-CTO Study Start-UP Project Manager (Hybrid)

Stanford University -
Stanford, CA

Apply Now

Job Details

Full-time
$86,248 - $100,158 a year

Qualifications

HIPAA compliance
HIPAA
Desktop applications
Research regulatory compliance
Productivity software
IRB compliance
Medical terminology
FDA regulations
Database software proficiency

Full Job Description

Study Start-up Project Manager - Hybrid

The Stanford Cancer Institute (SCI) is one of an elite number of National Cancer Institute-Designated Comprehensive Cancer Centers in the country, and is a prominent, dynamic, growing and complex Institute within the Stanford University School of Medicine. The SCI actively works to build synergies and collaborations among faculty with cancer-relevant expertise from four Schools and over 30 departments across Stanford University. We seek a Study Start-Up Project Manager to help us enact our mission to reduce cancer mortality through comprehensive programs of cancer research, treatment, education and outreach. Given the SCI’s mission, breadth, and depth, it employs over 320 staff members in a fast-paced, team-oriented, and forward-thinking environment with tremendous opportunities for personal and professional growth. The Clinical Trials Office (CTO) is an integral component of the Stanford Cancer Institute since the vital work performed there enables our adult and pediatric cancer centers to translate research from the laboratory into the clinical setting. You will be working with an unparalleled leading edge community of faculty and staff who are fundamentally changing the world of health care in the cancer arena.

Reporting to The Clinical Research Manager of Study Start-Up, the Study Start-up Project Manager will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to conduct industry sponsored trials, cooperative group trials, investigator initiated clinical research studies, from start up to close out. We are seeking candidates with excellent organizational skills, attention to detail, and outstanding oral/written communication skills with the ability to work with multi-disciplinary teams. Our staff run toward challenges, and you will have a demonstrated history of doing the same with a high degree of professionalism, initiative and flexibility.

Duties include*:

Oversee study start-up data management for cancer clinical trials. Develop and manage systems to organize, collect, report, and monitor data collection. Extract, analyze, and interpret data.
Develop project schedules, targets, measurements, and accountabilities, as assigned. Lead team meetings and prepare/approve minutes.
Formally supervise, train, and/or mentor new staff or students, as assigned, potentially including hiring, preparing or assisting with the preparation of performance evaluations, and performing related duties, in addition to instruction on project work.
Audit operations, to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes.
Collaborate with principal investigators and study sponsors, monitor and report serious adverse events, and resolve study queries.
Provide leadership in determining, recommending, and implementing improvements to policies/processes; define best practices.
Ensure regulatory compliance. Regularly inspect study document to ensure ongoing regulatory compliance.
- - Other duties may also be assigned

DESIRED QUALIFICATIONS:

Knowledge of clinical trials data management and clinical quality management
Clinical knowledge in the field of Thoracic
Knowledge of various projects and implementation strategies

EDUCATION & EXPERIENCE (REQUIRED):

Bachelor's degree in a related field and two years of experience in clinical research, or an equivalent combination of education and relevant experience.

KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):

Strong interpersonal skills
Proficiency with Microsoft Office and database applications.
Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices.
Knowledge of medical terminology.

CERTIFICATIONS & LICENSES:

Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.

PHYSICAL REQUIREMENTS*:

Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping.
Occasionally sit, reach above shoulders, perform desk based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.
Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.
- Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.

WORKING CONDITIONS:

Position may at times require the employee to work with or be in areas where hazardous materials and/or exposure to chemicals, blood, body fluid or tissues and risk of exposure to contagious diseases and infections.
May require extended or unusual work hours based on research requirements and business needs.

WORK STANDARDS:

Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned.
Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide, http://adminguide.stanford.edu.

*The expected pay range for this position is $86,248 to $100,158 per annum. *

At Stanford University, base pay represents only one aspect of the comprehensive rewards package. The Cardinal at Work website (https://cardinalatwork.stanford.edu/benefits-rewards) provides detailed information on Stanford’s extensive range of benefits and rewards offered to employees. Specifics about the rewards package for this position may be discussed during the hiring process.

Consistent with its obligations under the law, the University will provide reasonable accommodations to applicants and employees with disabilities. Applicants requiring a reasonable accommodation for any part of the application or hiring process should contact Stanford University Human Resources by submitting a contact form.

Stanford is an equal employment opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.

The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks, and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned.

Apply Now

Refine Your Search

clinical trial manager jobs in mountain view ca

SCI-CTO Study Start-UP Project Manager (Hybrid)

Clinical Data Manager - II

Global Clinical Trial Leader

Clinical Research Operations Program Manager

Clinical Research Manager

Clinical Trial Manager (CTM)

Project Manager

Clinical Data Manager

Sr. Clinical Study Manager

Senior Clinical Trial Manager (Sr CTM)

Senior Clinical Trial Manager - Job ID: 1955

Clinical Data Manager - T45 Labs

Clinical Trial Manager

Senior Clinical Study Manager

Clinical Trials Manager, Early Phase Oncology (Office Based)

Senior Clinical Study Manager

Interior Design Project Manager

Payer Healthcare Data Scientist, Manager

Clinical Project Manager - Pleasanton, CA

Clinical Trial Manager

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