Search jobs > Palo Alto, CA > Temporary > Clinical research coordinator

Clinical Research Coordinator 2

Stanford University
Palo Alto, California, US
$84.9K-$97K a year
Full-time

Stanford University is seeking a Clinical Research Coordinator 2 to conduct clinical research and work independently on progressively more complex projects / assignments.

Independently manage significant and key aspects of a large study or all aspects of one or more small research studies.

Please make sure you read the following details carefully before making any applications.

Duties include :

  • Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting / recruiting research participants and retaining participants in long-term clinical trials.
  • Oversee data management for research projects. Develop and manage systems to organize, collect, report, and monitor data collection.

Extract, analyze, and interpret data.

  • Develop project schedules, targets, measurements, and accountabilities, as assigned. Lead team meetings and prepare / approve minutes.
  • Formally supervise, train, and / or mentor new staff or students, as assigned, potentially including hiring, preparing or assisting with the preparation of performance evaluations, and performing related duties, in addition to instruction on project work.
  • Audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions / processes.

Monitor Institutional Review Board submissions, and respond to requests and questions.

  • Collaborate with principal investigators and study sponsors, monitor and report serious adverse events, and resolve study queries.
  • Provide leadership in determining, recommending, and implementing improvements to policies / processes; define best practices.
  • Develop study budget with staff and principal investigator, identifying standard of care versus study procedures. Track patient and study specific milestones, and invoice sponsors according to study contract.
  • Ensure regulatory compliance. Regularly inspect study document to ensure ongoing regulatory compliance.
  • Work with principal investigator to ensure Investigational New Drug applications are submitted to the FDA when applicable.

Ensure Institutional Review Board renewals are completed.

Other duties may also be assigned

EDUCATION & EXPERIENCE (REQUIRED) :

Bachelor's degree in a related field and two years of experience in clinical research, or an equivalent combination of education and relevant experience.

KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED) :

  • Strong interpersonal skills
  • Proficiency with Microsoft Office and database applications.
  • Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices.
  • Knowledge of medical terminology.

CERTIFICATIONS & LICENSES :

Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. May require a valid California Driver’s License.

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 :

  • Position may at times require the employee to work with or be in areas where hazardous materials and / or exposure to chemicals, blood, body fluid or tissues and risk of exposure to contagious diseases and infections.
  • May require extended or unusual work hours based on research requirements and business needs.

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.

The pay range for this position working in the California Bay area is $84,856.00-$97,021.00 / annually.

J-18808-Ljbffr

5 days ago
Related jobs
Promoted
Stanford University
Stanford, California

The Kwo Lab is seeking a Clinical Research Coordinator II (CRC2) to provide support for clinical research efforts in the Division of Gastroenterology and Hepatology. Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. Determine effect...

Promoted
Tekberry
Palo Alto, California

The Division of Pulmonary Allergy and Critical Care Medicine is seeking a temporary/casual Clinical Research Coordinator Associate (CRCA) at 100% time for 3 4-month period for a position to join the Lung Transplant Clinical Research Team and assist in the coordination of multiple clinical research p...

Promoted
Stanford Blood Center
Palo Alto, California

Stanford University’s Neuromuscular Division of Neurology is seeking a Clinical Research Coordinator Associate (CRCA) to join a neuromuscular research team dedicated to understanding and treating neuromuscular disorders. The position will coordinate the oversight and implementation of research proto...

Promoted
Stanford University (US)
Palo Alto, California

The Kwo Lab is seeking a Clinical Research Coordinator II (CRC2) to provide support for clinical research efforts in the Division of Gastroenterology and Hepatology. Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. The Division of ...

Promoted
Stanford University
Palo Alto, California

The Berger lab at the Stanford Department of Anesthesiology, Perioperative, and Pain Medicine, is seeking a Clinical Research Coordinator 2 (Fixed-term 2 years) to conduct clinical research and work independently on progressively more complex projects/assignments. Society of Clinical Research Associ...

Promoted
College of Charleston
Palo Alto, California

Stanford University is looking for an enthusiastic experienced Clinical Research Coordinator 2 to take on a leadership position in our team and independently manage significant and key aspects of large and multiple research studies at both Stanford's main campus and satellite sites. Society of Clini...

Apex Systems
Burlingame, California

Apex Systems is seeking a Clinical Research Coordinator to support data collection in the lab. Coordinate clinical technology validation studies, leading operational planning and day-to-day management of research execution. Serve as primary contact with research participants, vendors, and research l...

Promoted
College of Charleston
Palo Alto, California

The Kwo Lab is seeking a Clinical Research Coordinator II (CRC2) to provide support for clinical research efforts in the Division of Gastroenterology and Hepatology. Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. The Division of ...

TEKBERRY
Palo Alto, California

Job Description:</b></p> <p style="margin-right:5px; margin-bottom:10px">The Division of Pulmonary Allergy and Critical Care Medicine is seeking a temporary/casual Clinical Research Coordinator Associate (CRCA) at 100% time for 3 4-month period for a position to join th...

Cedars-Sinai
CA, United States

The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on e...