Clinical Research Coordinator | Temp to Hire | $$$$
This Jobot Consulting Job is hosted by : Ba Tran
Are you a fit? Easy Apply now by clicking the Apply button and sending us your resume.
Salary : $70,000 - $85,000 per year
A bit about us :
We are seeking an experienced Consulting Clinical Research Coordinator to join our healthcare team. This is an exciting opportunity to be part of a team that is at the forefront of clinical research in the healthcare industry. You will play a crucial role in managing and overseeing clinical trials, ensuring they are conducted in accordance with ethical standards and regulations. You will be directly involved in groundbreaking research that has the potential to significantly impact patient care and treatment outcomes in the field of Gynecologic Oncology (GynOnc). This position requires fluency in English and Spanish.
Why join us?
Medical , Dental and Vision Insurance
401K w / Match
Temp to Hire opportunity
PTO
Sick PTO
and more!
Job Details
- ENGLISH / SPANISH FLUENCY REQUIRED
Is your background a match?
Bachelor's degree in a related field preferred3+ years of experience in clinical research coordinationEnglish / Spanish fluency REQUIREDPrior experience in Gynecologic Oncology (GynOnc) is a plus!Excellent knowledge of clinical trial design, management, and regulatory requirementsStrong understanding of Good Clinical Practice (GCP) guidelinesExceptional organizational skills and ability to manage multiple clinical trials simultaneouslyExcellent communication and interpersonal skillsProficient in using clinical trial management systems and other related softwareAbility to work effectively in a team and independentlyDetail-oriented with strong problem-solving skillsProven ability to maintain confidentiality and handle sensitive information with discretionWillingness to stay updated on the latest trends, developments, and advancements in the field of GynOncCommitment to improving patient care and treatment outcomes through clinical researchNOTE : We are fully onsite (M-F) at our Fountain Valley, CA location; hybrid not availableWhat will you be doing?
Oversee the day-to-day management of clinical trials, including but not limited to, patient recruitment, data collection, and data analysisEnsure all clinical trials are conducted in accordance with the study protocol, ethical standards, and regulatory requirementsCoordinate with physicians, nurses, and other healthcare professionals to ensure patient safety and the integrity of clinical trial dataDevelop and maintain effective relationships with study sponsors, investigators, and other key stakeholdersPrepare and submit regular reports on the progress and results of clinical trialsParticipate in the development of study protocols, informed consent forms, and case report formsIdentify, evaluate, and manage potential risks and issues related to clinical trialsProvide training and guidance to other members of the clinical research teamStay updated on the latest trends, developments, and advancements in the field of GynOncInterested in hearing more? Easy Apply now by clicking the Apply button.
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