Clinical Research Coordinator - Surgical Oncology

National Medical Association; Los Angeles (CA); On-site; Full time

Job summary

The National Medical Association is seeking a full-time Clinical Research Coordinator to manage clinical research activities. The role involves oversight of study implementation and adherence to regulatory guidelines. Candidates should have a Bachelor's degree and relevant experience in study coordination. Strong communication and organizational skills are essential to thrive in this fast-paced environment.

Qualifications

• 1-3 years of previous study or clinical research coordination experience.
• Ability to work in a fast-paced environment with deadlines.
• Working knowledge of clinical research regulations and budgeting.

Responsibilities

• Implement and manage research activities for clinical studies.
• Plan tasks to ensure adherence to study protocols and regulations.
• Collaborate with diverse teams to support study administration.

Skills

Communication

Interpersonal Skills

Organizational Capabilities

Analytical Skills

Flexibility

Typing

Education

Bachelor's Degree

Tools

Spreadsheets

Data Entry Software

Job description

Description

The Department of Surgery is seeking a full time Clinical Research Coordinator to contribute to the overall operational management of clinical research / trial / study activities from design, set up, conduct, through closeout. In this position you will have responsibility for:

• The implementation of research activities for one or more studies.
• Recognizing and performing necessary tasks to manage projects and prioritizes work to meet necessary deadlines.
• Planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP).

The Clinical Research Coordinator collaborates with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support.

Pay Range: $33.63 - $54.11

Qualifications

Required:

• Bachelor's Degree or 1-3 years of previous study coordination or clinical research coordination experience
• Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport and build collaborate relationships.
• Strong organizational capabilities to organize multiple projects and competing deadlines forefficiency and cost-effectiveness.
• Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment.
• Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines
• Ability to respond to situations in an appropriate and professional manner.
• 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.
• Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry.
• Ability to navigate numerous software programs and applications.
• Ability to handle confidential material information with judgement and discretion.
• Working knowledge of the clinical research regulatory framework and institutional requirements.
• Mathematical skills sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinicaltrial budgets.
• Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) forclinical research.
• Be available to work in more than one environment, travel to meetings, off-site visits,conferences, etc.

Preferred:

• Spanish Speaking candidates are encouraged to apply.