Senior Clinical Research Coordinator

University of California

$95K — $115K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BS/BA degree in a related field or equivalent experience.
  • Demonstrated capability in developing complex recruitment strategies.
  • In-depth knowledge of clinical research regulations and protocols.
  • Strong project management skills for overseeing clinical trials.
  • Exceptional analytical and communication skills.
  • Ability to innovate in challenging environments and address complex issues.
  • Financial analysis expertise and experience with budget preparation.

Responsibilities

  • Coordinate and oversee multiple clinical studies independently.
  • Lead and provide guidance to junior research coordinators.
  • Implement and manage recruitment strategies for diverse patient populations.
  • Ensure compliance with clinical research contracts and FDA regulations.
  • Monitor operational management across multicenter clinical trials and local studies.
  • Develop and execute project plans, responding to audit risks and deadlines.
  • Maintain effective communication with stakeholders and contribute to problem-solving.

Benefits

  • Access to comprehensive health and wellness programs.
  • Opportunities for professional development and certification support.
  • Flexible work environment with an emphasis on work-life balance.
  • Engagement in impactful clinical research initiatives.
  • Collaboration with a team of experts in a leading research institution.
Full Job Description
Job Description

Please note: This is a limited appointment with 18 months duration. Senior Clinical Research Coordinators independently coordinate and are accountable for the overall administration of one or more clinical studies, typically requiring advanced-level knowledge and skills. They may provide leadership to lower-level clinical research coordinators and/or other support personnel. The position is responsible for, and critically important to the overall operational management of clinical research activities. It has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as a clinical database and biorepository.

Required Qualifications
  • BS/BA degree in a related area and/or equivalent experience/training. Sufficient experience and demonstrated skills to perform the assigned duties and responsibilities.
  • Sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities.
  • Demonstrated ability to develop recruitment strategies in complex environments and differing patient pools, independently identifying recruitment leads, implementing new strategies, and continually adjusting strategies to meet current recruitment goals.
  • In-depth knowledge of clinical research contracts and grants, clinical trials, protocols, FDA regulations, and complex visit structures.
  • Project management skills to oversee the administrative operations of the clinical trials program; knowledge of strategies for recruiting human subjects.
  • Exceptional analytical skills to evaluate the importance and urgency of problems; excellent demonstrated interpersonal, verbal and written communication skills.
  • Ability to analyze complex and non-routine issues requiring innovative solutions.
  • Ability to operate effectively in a changing organizational and technological environment.
  • Ability to assess and respond to audit risk; ability to develop project plans/schedules and motivate team to meet deadlines.
  • Ability to interpret and apply policies and regulations.
  • Financial analysis skills; demonstrated skills in preparing and presenting financial and quantitative analyses, including financial projections and budgets.
  • Significant project and clinical trial management experience or progressively responsible experience in a related position including regulatory and compliance responsibilities.
  • Experience using database software, such as REDCap or Medidata RAVE or other electronic data capture system.
  • Ability to obtain certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals within one year of date of hire.

Preferred Qualifications
  • Fluency in spreadsheet software; ability to develop complex spreadsheets independently; demonstrated skills in audit preparation, execution, and follow-up.
  • Experience in risk management regarding study subjects, federal and non-federal sponsors and regulating bodies.
  • Experience with grant application procedures, personnel documentation, contract generation and subcontracting, preferably at UCSF.
  • Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals.


Qualifications

License/Certification
  • Ability to obtain certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals within one year of date of hire.


Salary Information

The final salary and offer components are subject to additional approvals based on UC policy.

Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.

To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html

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