Budget Amendment Negotiator, Hematology / Oncology (Fully Remote)

Description

We are seeking an

experiencedBudget Amendment Negotiator who will be responsible for

regulatory coordination of clinical research studies within assigned units,

departments, or divisions. In this role, you will perform detailed reviews of

clinical research protocols and utilize that information to prepare, manage and

submit all required study / regulatory documents and all required applications

and forms related to internal UCLA requirements, FDA requirements, sponsor

requirements, etc. Additionally, you will work with study monitors to process,

review and collect the appropriate regulatory documents in a timely manner and

in compliance with federal, state, and university mandated laws, regulations

and policies.

The ideal candidate will

have at a minimum, 1+ years of budget / negotiating experience.

Salary offers are

determined based on various factors including, but not limited to,

qualifications, experience, and equity. UCLA Health hourly salary range for

this position is $31.51 - $62.64.

Qualifications

Required :

Minimum of 1+ years of experience as a clinical

researcher

Interpersonal skills to effectively communicate

information in a timely, professional manner and establish and maintain

cooperative and effective working relationships with students, staff,

faculty, external collaborators and administration and to work as a member

of a team.

Ability to set priorities and complete ongoing tasks

with competing deadlines, with frequent interruptions, to meet the

programmatic and department needs, while complying with applicable

University policies and federal and state regulations.

Analytical skills to assess clinical research protocols

and regulatory requirements, define problems, formulate logical solutions,

develop alternative solutions, make recommendations, and initiate

corrective actions.

Close attention to detail to ensure accuracy in a

fast-paced, fluctuating workload environment.

Organization skills to create and maintain

administrative and regulatory files effectively as well as independently

balance the various tasks to ensure deadlines are met.

Demonstrated proficiency with Adobe and Microsoft suite

software, especially Excel, to perform daily tasks efficiently and

accurately.

A learning and professional growth mentality so that

new software tools, systems, and processes can be adopted quickly and

efficiently.

Working knowledge of clinical research concepts,

policies and procedures, and human safety protection regulations and laws.

Knowledge of and experience working with a variety of

local and external IRBs, scientific review and other research committees,

national cooperative group sponsors, industry sponsors, federal and

foundation funding organizations, etc.