Clinical Research Analyst

Job Summary:

Applies extensive knowledge of clinical research protocols and processes to design research projects of large scope and high degrees of complexity. Effectively manages multiple projects and makes determinations on feasibility of clinical trials within the research group. Leads the operational and administrative functions of the neuromuscular research group.

You will required to be onsite a minimum of 1 day per quarter as of the date set by your manager or, if applicable, 30 days from letter send date. Your specific onsite schedule may vary based on operational and programmatic needs. Your manager retains discretion to modify onsite requirements as needed, consistent with University and School of Medicine policies.

Department Overview:

The mission of the Neuromuscular Division at UCSF is to provide the highest level of comprehensive and compassionate care to individuals affected by neuromuscular disorders. Our team of specialists is dedicated to advancing the understanding and treatment of these conditions through cutting-edge research, education, and innovation. We strive to improve the quality of life for our patients by promoting early diagnosis, individualized treatment plans, and a multidisciplinary approach to care. Our ultimate goal is to make a significant impact in the field of neuromuscular medicine and contribute to the global effort to find a cure for these debilitating disorders.

About UCSF

The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences. We bring together the world's leading experts in nearly every area of health. We are home to five Nobel laureates who have advanced the understanding of cancer, neurodegenerative diseases, aging and stem cells.

Pride Values

UCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity and excellence - also known as our PRIDE values.

In addition to our PRIDE values, UCSF is committed to equity - both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available here.

Join us to find a rewarding career contributing to improving healthcare worldwide.

Equal Employment Opportunity

The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.

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

Required Qualifications:

• Bachelor''s degree in related area and / or equivalent experience / training.
• CCRP
• Advanced knowledge of clinical research practices and philosophy, and ability to apply knowledge and skills to recommend improvements in methodology. Advanced knowledge of regulatory requirements.
• Advanced ability to effectively lead one or more projects with competing to meet the demands of a fast-paced and dynamic work environment. Adaptable to quickly changing priorities.
• Advanced ability to effectively lead one or more projects with competing to meet the demands of a fast-paced and dynamic work environment. Adaptable to quickly changing priorities.
• Advanced communication skills; including verbal and written, active listening, critical thinking, persuasiveness, advising and counseling skills. Clear and concise communicator.
• Advanced interpersonal skills, including but not limited to: problem-solving, teamwork development, leadership with other team members. Works well with others to achieve common goals.
• Proven ability to perform all commonly applicable functions in word processing and spreadsheet software. Advanced knowledge of clinical information and documentation application programs.
• Proven ability utilizing clinical trial management systems.
• In depth ability to work collaboratively with other cross-functional teams. In depth ability to interface, collaborate and influence / persuade other members of an extended study team.

Preferred Qualifications:

• Master's degree in a neurosciences field
• Prior experience working on clinical trials for ALS and neuromuscular diseases

DUTIES & ESSENTIAL JOB FUNCTIONS

%

of time

Essential Function (Yes/No)

Key Responsibilities

(To be completed by Supervisor)

20

Yes

Functions as a lead in developement of new processes and protocols with project team for highly complex clinical trials. Oversees and manages protocol amendments.

5

Yes

Monitors, evaluates and coordinates data from multiple systems to recommend new actions / procedures from research analysis. Participates in preparation of manuscripts, abstracts and scientific presentations.

5

Yes

Conducts large project feasibility assessments. Analyzes risks, strategies and solutions. Develops project timelines and key milestones for assigned projects. Recommends adjustments to budgets and vendor agreements as necessary.

10

Yes

Assesses policies and processes to ensure the proposed project plan is compliant with applicable guidelines. Revises research / trial documents so they are consistent with protocol revisions.

10

Yes

As a technical lead, provides guidance to all levels of management on ways to improve effectiveness. Proactively recommends interventions / corrective actions to meet project goals.

10

Yes

Ensures reporting is consistent with external guidelines, university policies and regulations.

20

Yes

Functions as a lead with other team members. Provides direction and guidance to project team members.

20

Yes

Develops, manages and oversees the organizational, strategic and tactical aspects of a clinical trial program. Provides operational, clinical and project management oversight for assigned research.

0

0

0

0

100%

DUTIES & ESSENTIAL JOB FUNCTIONS

%

of time

Essential Function (Yes/No)

Key Responsibilities

(To be completed by Supervisor)

20

Yes

Functions as a lead in developement of new processes and protocols with project team for highly complex clinical trials. Oversees and manages protocol amendments.

5

Yes

Monitors, evaluates and coordinates data from multiple systems to recommend new actions / procedures from research analysis. Participates in preparation of manuscripts, abstracts and scientific presentations.

5

Yes

Conducts large project feasibility assessments. Analyzes risks, strategies and solutions. Develops project timelines and key milestones for assigned projects. Recommends adjustments to budgets and vendor agreements as necessary.

10

Yes

Assesses policies and processes to ensure the proposed project plan is compliant with applicable guidelines. Revises research / trial documents so they are consistent with protocol revisions.

10

Yes

As a technical lead, provides guidance to all levels of management on ways to improve effectiveness. Proactively recommends interventions / corrective actions to meet project goals.

10

Yes

Ensures reporting is consistent with external guidelines, university policies and regulations.

20

Yes

Functions as a lead with other team members. Provides direction and guidance to project team members.

20

Yes

Develops, manages and oversees the organizational, strategic and tactical aspects of a clinical trial program. Provides operational, clinical and project management oversight for assigned research.

0

0

0

0

100%