Job summary
Job post source
This job is directly from Irvine Clinical Research
Job overview
The Senior Clinical Research Coordinator will lead Phase II/III clinical trials in Neurology and Psychiatry, ensuring effective clinical operations and data management.
Responsibilities and impact
Daily responsibilities include coordinating clinical operations, performing study procedures, maintaining study data, collaborating with recruitment teams, conducting assessments, and mentoring junior staff.
Compensation and benefits
The position offers a starting salary of $95,000 per year, with negotiable higher salary for candidates with a nursing license, plus full health/dental/vision insurance and 3 weeks of PTO annually.
Experience and skills
Candidates must have at least five years of experience in industry-sponsored drug trials, with a strong ability to manage high-enrollment clinical trials and proficiency in CTMS.
Career development
Opportunities for professional growth include mentoring roles and potential advancement within the clinical research team.
Work environment and culture
The company values precision, attention to detail, and teamwork in a supportive clinical environment focused on CNS research.
Company information
Irvine Clinical Research specializes in late phase CNS clinical trials and is dedicated to advancing research in Neurology and Psychiatry.
Team overview
The candidate will join a team of experienced coordinators and research assistants, fostering a collaborative and productive work environment.
Job location and travel
This position is based in-person at the Alzheimer’s Orange County building in Irvine, California.
Application process
Interested applicants should submit their resumes and cover letters, with specific instructions provided on the company website.
Unique job features
The role offers unique opportunities to lead significant clinical trials and contribute to impactful research in CNS disorders.
Company overview
Irvine Clinical Research is a dedicated clinical trial center specializing in the testing of new medical treatments and therapies. They conduct Phase I-IV clinical trials, partnering with pharmaceutical companies to bring innovative healthcare solutions to market. Founded with a mission to advance medical science, the company has a history of contributing to significant medical breakthroughs. Their revenue is primarily generated through contracts with pharmaceutical firms and grants for conducting clinical trials.
How to land this job
Tailor your resume to highlight your extensive experience in coordinating Phase II/III clinical trials, particularly in Neurology and Psychiatry, to align with the specific needs of Irvine Clinical Research.
Emphasize your proficiency in adhering to GCP guidelines and managing both paper and electronic study data, as these are critical aspects of the Senior Clinical Research Coordinator role.
Apply through multiple channels such as the Irvine Clinical Research corporate site and LinkedIn to maximize your chances of being noticed for the position.
Connect with professionals in the clinical research division at Irvine Clinical Research on LinkedIn to gain insights and inquire about the position; potential ice breakers could include discussing recent advancements in CNS trials or expressing interest in their recruitment strategies.
Optimize your resume for ATS systems by incorporating keywords from the job description, such as 'clinical trials,' 'GCP,' 'CTMS,' and 'enrollment goals' to improve your chances of passing initial screenings.
Utilize Jennie Johnson's Power Apply feature to streamline your application process, ensuring your resume is tailored, and your networking efforts are efficient, allowing you to focus on preparing for interviews.
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