Clinical Research Coordinator

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Job details

Clinical Research Coordinator 6 Month Contract in San Francisco, CA.

This Jobot Consulting Job is hosted by Robert Reyes

Are you a fit? Easy Apply now by clicking the "Easy Apply" button and sending us your resume.

Salary $25 - $30 per hour

A Bit About Us

Clinical Research Coordinator 6 Month Contract in San Francisco, CA.

Prestige Hospital System

Placed #1 in both California in a broad assessment of excellence in hospital-based patient care.



Why join us?


Competitive Salary$$

Variety of benefits and perks designed to support your well-being and professional growth. Here are some of the key benefits

Health and Medical Benefits Comprehensive health plan options, including medical, dental, and vision coverage, as well as flexible spending accounts to offset medical costs.

Retirement Benefits Retirement plans to help you secure your financial future.

Tuition Benefits Free tuition for yourself or an immediate family member after two years of employment.

Time Off Paid and unpaid time off for vacation, personal health, and family care.

Clinical Research Coordinator 6 Month Contract in San Francisco, CA.

Well-being Programs Resources to support your physical, mental, and spiritual health.

Employee Discounts Discounts on sports tickets, gym memberships, event tickets, and more.

Professional Development Opportunities for growth and development through various training programs and resources.

If you are passionate, thrive in a fast-paced environment and are ready to take your career to the next level, we would love to hear from you.

Job Details

Clinical Research Coordinator 6 Month Contract in San Francisco, CA.

Job Details

We are looking for a dynamic, motivated, and experienced Consulting Clinical Research Coordinator to join our expanding team in the healthcare industry. The successful candidate will be responsible for coordinating and managing clinical research projects, ensuring all activities are conducted in accordance with the study protocol, institutional policies, and federal regulations. The role requires a strong understanding of CITI Training, Apex, Epic, Medrio, and Medidata. The ideal candidate will have a minimum of 5 years of experience in clinical research coordination.

Responsibilities

• Coordinate and manage all aspects of clinical research projects from initiation to close-out.
• Ensure all clinical research activities are conducted in accordance with the study protocol, institutional policies, and federal regulations.
• Provide consultation services to the research team regarding study design, data analysis, and interpretation of results.
• Collaborate with the research team to develop and implement recruitment strategies.
• Maintain accurate and complete study documentation including case report forms, consent forms, and regulatory documents.
• Use clinical research management systems such as Apex, Epic, Medrio, and Medidata to track study progress and manage study data.
• Provide training and guidance to research staff on study procedures and Good Clinical Practice (GCP).
• Perform data analysis and prepare reports for the research team and study sponsors.
• Participate in study monitoring visits and regulatory audits.
• Identify and resolve study-related issues and ensure participant safety and data integrity.
• Stay updated on the latest developments in clinical research regulations and best practices.
  
  

Qualifications

• Bachelor’s degree in a related field. A Master’s degree or equivalent is preferred.
• Minimum of 1 years of experience in clinical research coordination.
• Certified in CITI Training.
• Proficient in clinical research management systems such as Apex, Epic, Medrio, and Medidata.
• Excellent understanding of clinical research protocols, data collection methods, and evaluation metrics.
• Strong knowledge of Good Clinical Practice (GCP) and federal regulations related to clinical research.
• Excellent project management, organizational, and multitasking skills.
• Strong analytical skills and the ability to interpret complex clinical data.
• Excellent communication and interpersonal skills.
• Ability to work independently and collaboratively in a team.
• Proficient in Microsoft Office Suite.
• Must be detail-oriented and able to handle multiple projects simultaneously.
  
  

Join our team and contribute to the advancement of healthcare through clinical research. We offer a competitive compensation package and the opportunity to work in a challenging and rewarding environment. If you meet the above qualifications and are ready to take on this exciting role, we invite you to apply.

Interested in hearing more? Easy Apply now by clicking the "Easy Apply" button.

Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.

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Click our Jobot Consulting logo and follow our LinkedIn page!