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Description

The Department of Surgery is seeking to hire a full time Senior Clinical Research Coordinator. As the Senior CRC you will play a critical role in the overall operational management of clinical research / trial / study activities from design, set up, conduct, through closeout. You will have direct responsibility for the implementation 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. You will recognize and perform necessary project management tasks and prioritizes work to reach scheduled goals. In this role you are a technical leader, responsible for ensuring the study protocol and procedures have been completed accurately, safely, and in a timely manner. You may supervise and train others on projects, as necessary. And lastly, you will work with PIs, departments, sponsors, institutions, and other entities as needed to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of studies.

Pay Range: $38.6 - $61.87 hourly.

Qualifications

• Bachelor's Degree or three-to seven years of study coordination or clinical research coordination experience

• Ability to work efficiently and complete tasks with a high degree of accuracy.

• Ability to organize multiple projects for efficiency and cost-effectiveness.

• Analytical skills sufficient to work and solve problems.

• Ability to work flexible hours to accommodate research deadlines.

• Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines.

• Ability to be flexible in handling work delegated by more than one individual or in the course of delegating work.

• Strong interpersonal communication skills to effectively and diplomatically interact with others, including institutional leadership.

• Strong written communication skills, ability to compose advanced correspondence and manage large file systems.

• Advanced typing and computer skill/ability including word-processing, use of spreadsheets, email, and data entry.

• Ability to handle confidential material with judgement and discretion.

• Skill in managing diverse, complex tasks and information transfer among multiple constituents.

• Sufficient math ability and knowledge of clinical trials budgeting processes to manage the preparation of clinical trial budgets.

• Advance knowledge of the clinical research regulatory framework and institutional requirements.

• Ability to supervise and delegate clerical work as needed.

• Advanced knowledge of Good Clinical Practice (GCP) for clinical research

• Strong knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.

• Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc.

UCLA Health welcomes all individuals, without regard to race, sex, sexual orientation, gender identity, religion, national origin or disabilities, and we proudly look to each person’s unique achievements and experiences to further set us apart.