Top 120 Clinical study manager Jobs in South San Francisco Ca

Study Project Manager I - Hybrid
AbbVie —South San Francisco, CA
- $109,500 - $208,500 a year
- Full-time
- Hybrid work
- 6 years
- Bachelor's degree
- Experience equivalent to degree accepted
- Paid holidays
- Health insurance
5d
Cell and Gene Therapy Discovery Stage Project Manager
Stanford University —Stanford, CA
- $120,038 - $153,486 a year
- Full-time
- Hybrid work
- 5 years
- Office
- University
Assistant Clinical Research Coordinator
University of California San Francisco —San Francisco, CA
- Windows
- High school diploma or GED
- Organizational skills
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
SCI Study Start-UP Project Manager - GI (Hybrid)
Stanford University —Stanford, CA
- Extended hours
- Hybrid work
- HIPAA
- Mid-level
- Bachelor's degree
6d
Clinical Research Coordinator Cardiology
University of California San Francisco —San Francisco, CA
- HIPAA
- Mid-level
- High school diploma or GED
SCI-CTO Study Start-UP Project Manager (Hybrid)
Stanford University —Stanford, CA
- $86,248 - $100,158 a year
- Extended hours
- Hybrid work
- HIPAA
- Mid-level
- Bachelor's degree
Associate Manager / Manager, Project Services - Laboratories (Remote - West Coast)
IQVIA —San Francisco, CA
- $64,200 - $173,000 a year
- Full-time
- Remote
- Microsoft Excel
- Computer literacy
- Data analysis skills
- Work from home
Clinical Research Manager
University of California San Francisco —San Francisco, CA
- Full-time
- Nursing
- RN License
- BLS Certification
Clinical Research Manager
Stanford University —Stanford, CA
- $124,521 - $153,615 a year
- Extended hours
- Hybrid work
- 5 years
- HIPAA
- Master's degree
Clinical Trial Manager, CKD
Maze Therapeutics —South San Francisco, CA
- $143,000 - $175,000 a year
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator
University of California San Francisco —San Francisco, CA
- Full-time
- Microsoft Word
- Microsoft Excel
- Patient monitoring
6d
CLIN RSCH CRD AST
University of California San Francisco —San Francisco, CA
- Full-time
- Windows
- High school diploma or GED
- Organizational skills
Clinical Reseach Coordinator
University of California San Francisco —San Francisco, CA
- Full-time
- Microsoft Excel
- HIPAA
- Mid-level
Clinical Trial Manager (Retina)
4D Molecular Therapeutics —Emeryville, CA
- $150,000 - $170,000 a year
- Remote
- Microsoft Excel
- 6 years
- Microsoft Outlook
Clinical Trial Manager
Sagimet Biosciences —San Mateo, CA
- $90 - $100 an hour
- Hybrid work
- Nursing
- 3 years
- Analysis skills
14d
Project Manager
Stanford University —Stanford, CA
- Full-time
- Google Workspace
- HIPAA
- Mid-level
Clinical Research Coordinator
Stanford University —Stanford, CA
- $86,248 - $100,158 a year
- Extended hours
- HIPAA
- Mid-level
- University
Clinical Trial Manager/Sr Clinical Trial Manager
Erasca —South San Francisco, CA
- $145,000 - $190,000 a year
- Remote
- Medicine
- Inventory management
- 5 years
- Health savings account
- AD&D insurance
Cancer Clinical Research Coordinator 2 – GI (Hybrid)
Stanford University —Stanford, CA
- Extended hours
- Hybrid work
- HIPAA
- Mid-level
- Bachelor's degree
11d

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Study Project Manager I - Hybrid

AbbVie -
South San Francisco, CA

Apply Now

Job Details

Full-time
$109,500 - $208,500 a year
5 days ago

Benefits

Paid holidays
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance

Qualifications

Pharmaceutical company experience
Stakeholder management

Full Job Description

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

Purpose:

The Study Project Manager I drives the connection between science and operational delivery and ensures operational excellence in planning and execution of clinical research studies across all development stages. The Study Project Manager I is responsible for and ensures clinical research studies are executed with quality and efficiency, on-time, within budget, and meet company objectives. The Study Project Manager I achieves these objectives by bringing scientific acumen, strategic thinking, innovation, experience in clinical study operations management and stakeholder management to address risks and challenges. The Study Project Manager I serves as leader of one or more cross functional Clinical Study Teams, leading clinical operations from planning through to execution in a cross functional matrix environment.

Responsibilities:

Defines and drives the operational strategies and deliverables for one or more clinical studies
Responsible for executing clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures).
Proactively manages budget, timelines and study issues; brings scientific acumen, technical expertise and global mindset to drive achievement of study objectives
Leader of the cross functional Clinical Study Team
Leads clinical operations planning through to execution via cross functional matrix environment and influences cross functional stakeholders to drive milestone achievement
Effectively manages vendors and a diverse set of external stakeholders including site staff, Key Opinion Leaders and patient groups
Brings a growth mindset, demonstrated by a willingness to continuously learn, grow and adapt, give and receive feedback, see challenges as opportunities
Coaches and effectively supports cross functional team members, delegates and empowers to the right level, actively contributes to Development Operations community
Contributes towards operational efficiencies and brings innovative ideas to their teams and studies -Demonstrates excellent communication and problem solving skills
Puts patients and customers at the center of what we do
Navigates ambiguity and thrives even when not having all the information
On a given study responsible for (but not limited to) : the development of the clinical study design and associated systems, tools and documents, study budget creation and oversight, vendor selection, scope development, management and oversight of external vendors, proactively identifying risks and address and/or escalate study related issues and opportunities for efficiency, being an empowered decision maker on operational aspects of study execution and creating an inclusive and innovative environment where staff and studies/programs will succeed
Provide leadership to Study Management Associates – lead, delegate and support activities to deliver on study milestones

Qualifications

Bachelor’s Degree or equivalent degree is required
6 years of demonstrated pharma-related and/or clinical research related experience or equivalent required.
Preferred exposure in study initiation through study completion in Phase 1-4 and/or Medical Device Trial Experience

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of thisposting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless anduntil paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Apply Now

Refine Your Search

clinical study manager jobs in south san francisco ca

Study Project Manager I - Hybrid

Cell and Gene Therapy Discovery Stage Project Manager

Assistant Clinical Research Coordinator

Clinical Trials Manager, Early Phase Oncology (Office Based)

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

Clinical Research Coordinator Cardiology

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

Associate Manager / Manager, Project Services - Laboratories (Remote - West Coast)

Clinical Research Manager

Clinical Research Manager

Clinical Trial Manager, CKD

Clinical Research Coordinator

CLIN RSCH CRD AST

Clinical Reseach Coordinator

Clinical Trial Manager (Retina)

Clinical Trial Manager

Project Manager

Clinical Research Coordinator

Clinical Trial Manager/Sr Clinical Trial Manager

Cancer Clinical Research Coordinator 2 – GI (Hybrid)

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