
Cancer Clinical Research Coordinator Associate – Breast (Hybrid)
Stanford, CA · HybridJobSeen 1 day agoSeen in employer's feed 1 day ago
Most applications go out cold — see where you stand first. No sign-up to start.
Watch jobs like this. New roles like this one near Stanford, CA, by email.
Don't just apply. Show up ready.
Olive works from this exact posting.
At a glance
Olive lists jobs from US employers, including remote roles you can work from the United States.
Job overview
Stanford Cancer Institute seeks a Cancer Clinical Research Coordinator Associate for Breast Oncology. Reporting to the Cancer Clinical Research Manager, the coordinator manages trial data, enrolls and follows patients, and assists with regulatory and financial requirements. The role supports the Institute’s cancer research mission in a team-oriented environment and calls for strong communication, follow-through, professionalism, initiative, and flexibility.
Skills & qualifications
Skills
Qualifications
Full job description
Job Description
Cancer Clinical Research Coordinator Associate – Breast Oncology (Hybrid Work Schedule)
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 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 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 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.
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 beworking 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 Cancer Clinical Research Manager for Breast Oncology, the Cancer 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. We are seeking candidates with excellent both written and verbal communication skills and able to follow through with specifically assigned deliverables. 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 data management, enrolling, and following patients on trial.
DESIRED QUALIFICATIONS:
-
Knowledge of the principles of clinical research and federal regulations.
-
Familiarity with IRB guidelines and regulations.
-
Previous experience with clinical trials.
-
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, http://adminguide.stanford.edu .
Similar jobs, posted recently
Open roles like this one, listed in the last 30 days.
Scientific Associate Product Marketing ManagerSynthego · Remote · US · $80–105K/yrPosted 1w agoPosted 1w ago
Court Witness CoordinatorInternal Revenue Service · San Jose, CA · $62–110K/yrPosted 1w agoPosted 1w ago
Recruiting CoordinatorParallel · Palo Alto, CA · $90–130K/yrPosted 2w agoPosted 2w ago
Social Worker (Program Coordinator)-HHAVeterans Health Administration · San Bruno, CA · $126–164K/yrPosted 1 day agoPosted 1 day ago- Recruiting CoordinatorSpaceXSI · Palo Alto, CA · $80–100K/yrPosted 3w agoPosted 3w ago
You've read the whole posting — now see how you match it.