administrative coordinator - 815 residential services

advanced practice manager cancer center infusion

assistant clinical research coordinator - cancer immunotherapy program

associate medical director of occupational health services (ohs) at ucsf benioff children's hospital oakland

recruiting coordinator Jobs in San Francisco

recruiting coordinator

administrative coordinator - 815 residential services Jobs in San Francisco

advanced practice manager cancer center infusion Jobs in San Francisco

assistant clinical research coordinator - cancer immunotherapy program Jobs in San Francisco

associate medical director of occupational health services (ohs) at ucsf benioff children's hospital oakland Jobs in San Francisco

clinical research coordinator thoracic oncology and sarcoma program

University of California - San Francisco

<div><div>The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Manager, Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.</div></div>

Clinical Research Coordinator - Thoracic Oncology and Sarcoma Program

<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.
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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.
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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

<div><div>The Helen Diller Family Comprehensive Cancer Center (HDFCCC) is seeking a Clinical Research Coordinator (CRC) to join the Cancer Immunotherapy Program within the Division of Hematology/Oncology. The Clinical Research Coordinator will perform independently to execute, manage, and coordinate research protocols, as directed by the Clinical Research Manager and/or the Principal Investigator (PI). The incumbent will coordinate the operations and data collection of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.</div></div>

Clinical Research Coordinator - Cancer Immunotherapy Program

<div><div>The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Lead Clinical Research Coordinator, Principal Investigator (PI), and/or the Research Personnel Manager for the Investigational Trials Unit, specifically for Genitourinary Oncology program; may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.</div></div>

Clinical Research Coordinator (2/4)

<div><div>The Helen Diller Family Comprehensive Cancer Center (HDFCCC) is seeking a Clinical Research Coordinator (CRC) Supervisor for the Cutaneous Oncology Program. Under the supervision of the Clinical Research Manager (CRM), the CRC Supervisor is tasked with managing and facilitating the day-to-day operations of their direct reports including training and supervising a team of three to six CRCs. The CRC Supervisor is responsible for training and evaluating CRC performance in executing studies, direct oversight of data collection and reporting, and implementation of protocols within the program that meet federal, state and institutional policies and guidelines. The CRC Supervisor assists the CRM in resolving operational, workload, protocol implementation, and data collection issues.</div></div>

Clinical Research Supervisor - Cutaneous Oncology Program

Medpace

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  Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team!
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 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
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  PACE
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 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.
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  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.
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  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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  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);
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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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  Compensation
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 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.
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  Medpace Overview
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 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.
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  Why Medpace?
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 People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
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 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.
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  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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  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
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  What To Expect Next
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 A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)

<div><div>This Nurse Practitioner (NP) position is assigned to the Cancer Services Medical Oncology clinics. In collaboration with the supervising physician and the administrative supervisor, the NP cares for patients receiving treatment for cancer. The NP provides clinical guidance for patients receiving systemic therapy for cancer including management of treatment toxicities, management of oncologic emergencies, symptom management, care coordination, assistance with triage, and other duties as assigned.
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The UCSF Helen Diller Family Comprehensive Cancer Center is an accredited National Cancer Institute Comprehensive Cancer Center. The NCI-Designation recognizes the scientific leadership, resources, and the depth and breadth of the research in basic, clinical and population science. As a Comprehensive Cancer Center, we demonstrate the added depth and breadth of research as well as substantial transdisciplinary research that bridges these scientific areas. The clinical services encompass adult and pediatric tumors across three campuses as well as regional satellite locations. The clinical cancer program is one of the largest clinical services at UCSF Medical Center and encompasses roughly 230 non-physician FTEs, 100+ cost center, and dozens of grant and philanthropic funding sources. At the UCSF Helen Diller Family Comprehensive Cancer Center we are truly pioneering care and leaders in all areas of cancer clinical care and research. We are routinely voted a top 10 program by U.S. News and World Report.</div></div>

Resource Nurse Practitioner

Explore 425+ Clinical research coordinator thoracic oncology and sarcoma program in San Francisco this April. Find roles across top companies and apply now to boost your career.