-
Tempus Redwood City, United StatesPassionate about precision medicine and advancing the healthcare industry? · We are seeking a highly motivated and capable bioinformatics scientist with experience and interest in translational cancer research and clinical genomics. This position requires experience with scientif ...
-
Tempus Redwood City, CA, United StatesPassionate about precision medicine and advancing the healthcare industry?Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidenc ...
-
BeiGene San Mateo, United States**General Description:** · The Executive Director, Clinical Development will effectively lead BeiGene clinical assets through successful development of early and late phase clinical development strategies and deliverables in partnership with multiple functions across the organiza ...
-
BeiGene Emeryville, United StatesSenior Field Medical Director, Southcentral, Solid Tumors, WY, CO, NM, TX, OK, LA, AR · This role is similar to the **Senior Medical Science Liaison** role and an individual contributor role. · The **Senior Field Medical Director (FMD)** will support BeiGene Pre-Clinical and Clin ...
-
BeiGene Emeryville, United StatesSenior Field Medical Director, Southcentral, Solid Tumors, WY, CO, NM, TX, OK, LA, ARThis role is similar to the **Senior Medical Science Liaison** role and an individual contributor role.The **Senior Field Medical Director (FMD)** will support BeiGene Pre-Clinical and Clinical p ...
-
BeiGene Emeryville, United StatesSenior Field Medical Director, Southcentral, Solid Tumors, WY, CO, NM, TX, OK, LA, AR · This role is similar to the **Senior Medical Science Liaison** role and an individual contributor role. · The **Senior Field Medical Director (FMD)** will support BeiGene Pre-Clinical and Cl ...
-
Stanford University Stanford, United States Full timeCancer Clinical Research Coordinator Associate – Pediatric Oncology, Solid Tumor (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 ...
-
Stanford University Stanford, United StatesInclude - : Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist Clinical Research, Research Co ...
-
Associate Director, Oncology Market Planning
1 week ago
Summit Therapeutics Sub, Inc. Menlo Park, United States**Our Mission**: · We have in-licensed Ivonescimab, which is a novel, potential first-in-class investigational bispecific antibody combining the effects of immunotherapy via a blockade of PD-1 with the anti-angiogenesis effects associated with blocking VEGF into a single molecule ...
-
Life Science Research Professional 1
3 weeks ago
Stanford University Stanford, United StatesLife Science Research Professional 1 - Heitzeneder Lab Onsite Work Agreement · Stanford University is seeking a computational Life Science Research Professional 1 to perform basic analytical functions and activities in defined research projects and independently conduct bioinform ...
-
Head of Regulatory Affairs, Oncology
3 weeks ago
Ascendis Pharma Palo Alto, United StatesHybridPalo Alto, California, United StatesOncology, Regulatory, OncologyFull time1404 · Description · We are a dynamic, fast-growing biopharma company with offices in Denmark, Germany, and the United States. Today, we're advancing programs in Endocrinology Rare Disease, and Oncol ...
-
Associate Director, Formulation Development
3 weeks ago
Pliant Therapeutics, Inc. South San Francisco, United StatesPliant is conducting a Phase 1 study for its third clinical program, PLN-101095, a small molecule, dual-selective inhibitor of αvß8 and αvß1 integrins, that is being developed for the treatment of solid tumors. The Company also has discovery and development programs in oncology a ...
-
Principal Quality Control Specialist
2 weeks ago
Arsenal Biosciences Hayward, United StatesArsenalBio, a privately held, clinical-stage programmable cell therapy company engineering advanced CAR T therapies for solid tumors, is seeking a talented Principal Quality Control Analyst to work onsite based in our Hayward office.ArsenalBio's mission is to develop efficacious ...
-
Associate Director, Clinical Business Operations
3 weeks ago
Arsenal Biosciences South San Francisco, United StatesArsenalBio, a privately held programmable cell therapy company engineering advanced CAR T therapies for solid tumors, is seeking a talented Associate Director, Clinical Business Operations to work hybrid or remotely.ArsenalBio's mission is to develop efficacious and safe cellular ...
-
Mechanical Eng Ii
3 weeks ago
Medtronic Santa Clara, United States**Careers that Change Lives · **At our R&D Department in Medtronic Neuromodulation, we focus on the development of cutting-edge medical devices in the Neuromodulation area. Interventional Pain develops mínimally invasive therapies that treat musculoskeletal pathologies such as ve ...
-
Hospital Unit Service Coordinator
2 weeks ago
University of California San Francisco San Francisco, United StatesThe Unit Service Coordinator (USC), under direction of the Patient Care Unit Manager, Nursing Supervisor, or Charge Nurse, functions as the source of the focal communication within the patient care unit and performs administrative functions directed toward positive patient care o ...
-
Medical Director, Drug Safety
4 days ago
People With Chemistry San Carlos, United States(Sr.) Medical Director, Drug Safety Remote Based Oncology-Hematology | Cell Therapy Pay Range: $280,000 - $340,000 Overview: Meet are exclusively partnering with a mid-sized biotech who have developed a T-cell based immunotherapy platform targeting both solid and liquid tumors. O ...
-
Senior Accountant
2 weeks ago
Cargo Therapeutics San Carlos, United States· CARGO Therapeutics is looking for an experienced, knowledgeable, and highly organized Senior Accountant to join our Finance team. · The Senior Accountant will join a growing and a dynamic Finance team and interact with various functions in the organization. Reporting to the A ...
-
Senior Accountant
3 weeks ago
Cargo Therapeutics San Carlos, United States· CARGO Therapeutics is looking for an experienced, knowledgeable, and highly organized Senior Accountant to join our Finance team. · The Senior Accountant will join a growing and a dynamic Finance team and interact with various functions in the organization. Reporting to the A ...
-
BioSpace Redwood City, United StatesJob Details · JOIN US · Adicet Bio, Inc. is a clinical stage biotechnology company discovering and developing allogeneic gamma delta T cell therapies for cancer. Adicet is advancing a pipeline of "off-the-shelf" gamma delta T cells, engineered with chimeric antigen receptors (CAR ...
cancer clinical research coordinator associate pediatric oncology, solid tumor - San Carlos, United States - Stanford University
Description
Cancer Clinical Research Coordinator Associate Pediatric Oncology, Solid Tumor (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 Cancer Clinical Research Coordinator Associate to help us enact our mission to reduce cancer mortality through comprehensive programs of cancer research, treatment, education and outreach.
Given the SCIs 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 Cancer Clinical Trials Office (CCTO) 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 Clinical Research Manager for Pediatric Oncology, the Clinical Research Coordinator Associate will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to manage data, enroll and follow patients on trial and assist with regulatory and financial requirements of the trials.
This position will focus on solid tumor clinical trials, though may be asked to assist with other trials within the Pediatric Oncology portfolio as needed.
We are seeking candidates with excellent written and verbal communication skills, attention to detail, and the ability to independently problem solve.
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.
Responsibilities include enrolling and following patients on trial, collecting study data, and interacting with clinicians and study sponsors to carry out trial activities.
Core duties include*:
Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out.
Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies.
Coordinate collection of study specimens and processing.
Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms.
Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure Institutional Review Board renewals are completed.
Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
Participate in monitor visits and regulatory audits.
*-Other duties may be assigned.
DESIRED QUALIFICATIONS:
Knowledge of the principles of clinical research and federal regulations.
Familiarity with IRB guidelines and regulations.
Previous experience with clinical trials, oncology, and/or pediatrics.
Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.
EDUCATION & EXPERIENCE (REQUIRED):
Two-year college degree and two years related work experience or a Bachelors degree in a related field or an equivalent combination of related education and relevant experience.
Strong interpersonal skills.
Proficiency with Microsoft Office.
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:
Occasional evening and weekend hours.
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,The expected pay range for this position is $31.73 to $36.54 per hour.
Stanford University provides pay ranges representing its good faith estimate of what the university reasonably expects to pay for a position.
The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs.
At Stanford University, base pay represents only one aspect of the comprehensive rewards package. The Cardinal at Work website ) provides detailed information on Stanfords 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.
