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research assistant

academic human resources analyst 3 Jobs in San Francisco

academic human resources analyst 3

academic personnel analyst 2 Jobs in San Francisco

academic personnel analyst 2

administrative analyst Jobs in San Francisco

administrative analyst

research associate

University of California - San Francisco

<div><div>The Shy Lab in the UCSF Department of Laboratory Medicine is recruiting a Staff Research Associate (SRA) to assist with cutting-edge cellular engineering projects. Our lab develops novel genome/epigenome editing strategies to reprogram human immune cells for therapeutic applications: including cancer, genetic diseases, and neurodegeneration. In this role, the SRA will explore state-of-the-art methods for genetically engineering primary human immune cells &ndash; with the goal of reprogramming these cells to perform new therapeutic functions in the brain. This position is well-suited for candidates interested in applying to PhD or MD/PhD programs within 2-3 years. Located in the Gladstone-UCSF Institute for Genomic Immunology, the Shy Lab is a highly collaborative and interdisciplinary academic environment.</div></div>

Staff Research Associate

<div><div>The laboratory of Dr. David Oh conducts translational research focusing on the intersection of immunology and oncology. The research associate will work closely with Dr. Oh on multiple research projects, with the objective of identifying novel ways to use innate immunity to cure cancer, and exploring mechanisms of immunotherapy. The position involves designing and executing experiments using human blood and tissue samples, in vitro culturing of human lymphocytes, functional experiments using cell culture protocols and flow cytometry techniques, data analysis, and minimal lab management, including collection and maintenance of a human specimen research bank. The associate may have the opportunity to contribute to publications, grants, and to present new findings at national scientific and clinical conferences.</div></div>

Staff Research Associate - Translational Research

<div><div>The Department of Pathology at UCSF aims to achieve the highest standards in patient care, research and education. The Department provides diagnostic pathology services in a wide variety of subspecialties with highly trained subspecialists who are recognized nationally and internationally for their expertise. The Department&rsquo;s research programs are diverse and interface with a wealth of basic and translational research programs that are a hallmark of UCSF. Our educational programs include a research-intensive academic residency program and fellowships in cytopathology, dermatopathology, gastrointestinal and liver pathology, gynecologic pathology, neuropathology and surgical pathology. Incumbent will be part of a major project discovering mechanisms of tumor resistance to immunotherapy, including CAR T cells and checkpoint blockade, in various types of cancer.
</div><div>To this end, incumbent will perform mouse work (tumor cell and CAR T cells injections, monitoring, harvests), multi-parameter flow and mass cytometry (CyTOF), fluorescence-activated cell sorting (FACS), multiplexed fluorescence microscopy and single-cell RNA sequencing; prepare RNA and DNA; perform PCR, weaning, tail biopsy, and blood processing; maintain records of mice; and perform other duties as assigned. Incumbent is expected to work well as part of a team and have enthusiasm for the practice of science.</div></div><div></div>

Staff Research Associate, Pathology

Medpace

<div>
 
 Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team!
 
 
 
 This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our
 
 PACE
 
 
 &reg;
 
 Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a competitive salary.
 
 
 
 WE OFFER THE FOLLOWING
 
 
 
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 Competitive travel bonus;
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 Equity/Stock Option program;
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 Training completion and retention bonus
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 Annual merit increases;
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 401K matching;
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 The opportunity to work from home;
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 Flexible work hours across days within a week;
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 Retain airline reward miles and hotel reward points;
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 Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere;
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 In-house travel agents, reimbursement for airline club, and TSA pre-check;
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 Opportunity for leadership positions &ndash; Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager, and many more;
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 CRA training program (PACE&reg;);
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 Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts;
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 In-house administrative support for all levels of CRAs; and
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 Opportunities to work with international team of CRAs.
 
 
 </li>
 </ul>
 
 Responsibilities
 
 
 
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 Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
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 Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;
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 Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
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 Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements;
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 On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward;
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 Verification that the investigator is enrolling only eligible subjects;
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 Regulatory document review;
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 Medical device and/or investigational product/drug accountability and inventory;
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 Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
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 Assess the clinical research site&rsquo;s patient recruitment and retention success and offering suggestions for improvement; and
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 Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.
 
 
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 </ul>
 
 Qualifications
 
 
 
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 Must have a minimum of a Bachelor&rsquo;s degree in a health or science related field;
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 Experience as a Clinical Research Coordinator (minimum 1 year);
 </li>
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 Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely;
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 Must maintain a valid driver&rsquo;s license and the ability to drive to monitoring sites;
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 Proficient knowledge of Microsoft&reg; Office;
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 Strong communication and presentation skills; and
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 Must be detail-oriented and efficient in time management.
 
 
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 </ul>
 
 Compensation
 
 
 
 A target salary range of $60,000 - $140,000 with potential for bonus and equity awards. Your compensation will be based on your skills and experience. Medpace offers the following benefits for full-time positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&amp;D insurance, pet insurance, and reimbursement for travel expenses (including food and gas allowance, rental cars, and hotel accommodations). For more details, please discuss with your recruiter.
 
 
 
 Medpace Overview
 
 
 
 Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
 
 
 
 Why Medpace?
 
 
 
 People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
 
 
 The work we&rsquo;ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
 
 
 
 Medpace Perks
 
 
 
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 Flexible work environment
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 Competitive PTO packages &ndash; starting at 20+ days
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 Company-sponsored employee appreciation events
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 Employee health and wellness initiatives
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 Competitive compensation and benefits package
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 Structured career paths with opportunities for professional growth
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 Discounts for local businesses
 
 
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 </ul>
 
 Awards
 
 
 
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 Named a Top Workplace in 2024 by The Cincinnati Enquirer
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 Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
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 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
 
 
 </li>
 </ul>
 
 What To Expect Next
 
 
 
 A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
 
 
</div>

Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)

<div><div>The Gynecologic Oncology program has a multi-disciplinary team that works closely with patients, providing the resources and close cooperation of many specialists with deep expertise in diagnosing and treating cancer. Our physician-scientists are also researching and developing new and effective treatments for Gynecologic cancer, including clinical trials. The Gynecologic Oncology program is seeking a Clinical Research Coordinator with an interest in women&rsquo;s health to have oversight over multiple clinical research projects and support our growing program.
 
 
The Clinical Research Coordinator (CRC) will independently, or with general direction, execute, manage, and coordinate clinical research protocols, as directed by the Clinical Research Manager, Principal Investigator (PI), and/or the Associate Director of Clinical Research Programs for the Early Phase program. The CRC will coordinate the administrative, data, and patient scheduling operations of several concurrent clinical research studies under the guidelines of research protocols and regulatory policies. The CRC will assist in the care of early and late-stage Gynecologic cancer patients while they participate in phase1b - phase 3 clinical trials.
 
 
The duties may include, but will not be limited to, supporting the management and coordinating the tasks of single or multiple clinical research studies; managing and updating databases to ensure data integrity; acting as intermediary between sponsors, research staff, and various UCSF departments; help assure compliance with all relevant regulatory agencies;; maintaining relevant regulatory documents in partnership with the Regulatory department; reporting study progress to investigators; participating in any internal and external audits or reviews of study protocols; and performing other duties as assigned.</div></div>

Clinical Research Coordinator - Gynecologic Oncology

UCSF Health

<div>
 
 Job Description
 
 
 
 
 Candidates must be fluent in Spanish
 
 
 
 The Research Assistant will provide research and administrative support to the principal investigator(s) (PI) of the assigned project(s). The incumbent will assist the PI in meeting the objectives of a HRSA-funded curricular development grant within the Division of General Internal Medicine, including data collection through review and analysis of qualitative and quantitative educational data, creating educational materials and presentations, assistance with writing study reports and IRB applications, and assistance in preparing scholarly articles and presentations. The incumbent will help manage applications for new funding opportunities. The incumbent will also provide administrative support to the PI, including scheduling, processing reimbursements and assisting with submitting manuscripts for publication.
 
 
 More specifically, the incumbent will conduct research operations such as:
 
 
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 Collaborating on design, documentation, and implementation of curricular innovations and program evaluation
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 Collecting data via surveys, focus groups, and interviews
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 Conducting literature reviews and systematic reviews
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 Developing and maintain research gathering, retrieval and reporting systems.
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 Cleaning, managing, and analyzing data
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 Conducting statistical studies in support of research proposals and protocols.
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 Coordinating research/program team meetings, taking notes, managing project timelines, and ensuring follow-up of deliverables
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 Preparing and submitting scientific manuscripts
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 Developing scientific presentations in partnership with the PI
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 Applying principles in stakeholder engagement for large-funded projects and grant applications
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 Managing project budgets for participant compensation, reimbursement, and other study supplies
 
 
 </li>
 </ul>
 And the incumbent will also support the PI by managing administrative operations. This includes:
 
 
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 Assist with scheduling meetings with the PI, study team, collaborators, and research participants
 </li>
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 Drafting and editing correspondence
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 Attending study-related meetings keep minutes, and perform other duties as assigned
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 When possible, developing policies and procedures to ensure that the team&rsquo;s operations, including its file and project management systems, collaboration tools, and dissemination activities run smoothly and efficiently.
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 When applicable, assisting in supervising and coaching early career employees to support research activities and study coordination
 
 
 </li>
 </ul>
 Flexibility and willingness to adapt to the evolving needs of the program are essential for success in this position.
 
 
 
 Qualifications
 
 
 
 
 Required Qualifications:
 
 
 
 <ul>
 <li>
 Bachelor's degree in public health, psychology, sociology, epidemiology or related area; and / or equivalent experience / training
 </li>
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 1+ years related experience
 </li>
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 Fluent in verbal and written Spanish; able to interview research participants in Spanish, transcribe responses in Spanish and communicate with research participants in Spanish
 </li>
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 Advanced academic writing and editing skills
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 Knowledge of design software (i.e. Adobe Photoshop, Illustrator; Power Point; etc.)
 </li>
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 Knowledge of statistical analysis software (i.e. Stata; SPSS; R; etc.)
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 Ability to work with electronic data collection tools (i.e. REDcap; Qualtrics; Dedoose)
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 Well-developed organizational and documentation skills; ability to attend to details
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 Excellent verbal and written communication and presentation skills; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team
 </li>
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 Proficiency with Microsoft Office
 </li>
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 Ability to work effectively in team-based environment; ability to prioritize tasks and meet multiple deadlines
 
 
 </li>
 </ul>
 
 Preferred Qualifications
 
 
 
 <ul>
 <li>
 College coursework in public health, psychology, or related field
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 <li>
 Master&rsquo;s degree in public health, psychology, or related field
 </li>
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 CITI Program &ndash; Human Subjects Research
 
 
 </li>
 </ul>
 
 About UCSF
 
 
 
 
 ABOUT US
 
 
 
 The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences. We bring together the world&rsquo;s leading experts in nearly every area of health. We are home to five Nobel laureates who have advanced the understanding of cancer, neurodegenerative diseases, aging and stem cells.
 
 
 
 Pride Values
 
 
 
 UCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity and excellence &ndash; also known as our PRIDE values .
 
 
 In addition to our PRIDE values, UCSF is committed to equity &ndash; both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available here .
 
 
 Join us to find a rewarding career contributing to improving healthcare worldwide.
 
 
 
 Equal Employment Opportunity
 
 
 
 
 The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.
 
 
 
 
 Salary Information
 
 
 
 The final salary and offer components are subject to additional approvals based on UC policy.
 
 
 Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.
 
 
 To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html
 
 
 
 About The Team
 
 
 
 The Department of Medicine is the largest department at Zuckerberg San Francisco General (ZSFG) with an annual budget of over $205 million. The Department is divided into 13 divisions and 3 centers. There are 148 fulltime faculty members, and 111 without-salary faculty affiliated with the Department. In addition, there are 420 staff employees, 73 MSP physician appointments, 31 non-faculty academics, 39 post- doctoral scholars, 10 clinical fellows, 67 fellow and resident FTEs, including 3.0 FTE chief residents. The Department operates more than 13 clinics, 4 inpatient medicine services with 9 teams (Resident Inpatient Service -5 teams, Faculty Inpatient Service - 3 teams, Cardiology Service -1 team and MICU Service -1 team), and 15 consultation services. The ZSFG Medicine Service has an annual volume of ~5600 hospital discharges, 52,000 clinical visits, 31,000 specialty care visits, and 18,000 eConsults. In terms of extramural funding, in 2023, ZSFG DOM principal investigators received new awards totaling $166M and earned research revenue of $135M.
</div>

Research Assistant

<div>Focuses on the organization, management, and archiving of research data for a variety of studies, projects, and initiatives. Supports research programs by ensuring data integrity, accessibility, and compliance with institutional guidelines for secure data handling and storage. Assists with the development and implementation of data management protocols, maintains detailed documentation of data workflows, and collaborates with research team members to ensure proper data organization and version control. Provides support for data queries, tracking, and updates to facilitate efficient project progression and reporting. 
The Research Assistant is ideally suited for recent university graduates who want to gain research experience and strengthen their preparation for MD or PhD studies after earning a Bachelor&rsquo;s or Master&rsquo;s degree. The anticipated term for this position is one year. The primary focus of this role is supporting multicenter pediatric trauma research by organizing, archiving, and managing large multimodal datasets, as well as contributing to analytical studies related to machine learning, clinical decision rules, and time-to-intervention evaluations. 
Responsibilities include curating, organizing, and archiving research data across multiple studies; maintaining meticulous version control and data documentation; collaborating closely with research fellows, data scientists, and faculty on dataset development and preparation for analysis; assisting with data exploration, quality control, and troubleshooting; synthesizing literature related to trauma, clinical decision rules, and diagnostic imaging; and preparing research reports, abstracts, and figures for presentations and publications. 
This role offers the opportunity to develop essential research and data management skills using real-world clinical datasets, with exposure to advanced computational tools and professional development through collaboration with multidisciplinary teams. Candidates with interests in clinical research, pediatric emergency medicine, computer vision, or data science are highly encouraged to apply. The ideal candidate is self-directed, detail-oriented, and an effective communicator in both written and spoken English. Prior research experience is a plus but not required.</div>

Explore 172+ Research associate in San Francisco this April. Find roles across top companies and apply now to boost your career.

172 research associate jobs In San Francisco

Staff Research Associate

Staff Research Associate - Translational Research

Staff Research Associate, Pathology

Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)

Clinical Research Coordinator - Gynecologic Oncology

Research Assistant

Research Assistant