Clinical Research Coordinator

Responsibilities

Communicate on a regular basis with Study Sponsor’s, CRO’s, staff, etc. regarding questions, concerns, as well as status of the protocol

Monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study

Create/review forms created or revised for assigned trials to assure protocol compliance

Maintain files using standardized study document labeling and filing procedures

Implement initial protocol and amendments, training staff who will be involved in patient treatment and management

Maintain an up-to-date contact list

Assist with patient screening and determination of eligibility

Facilitate the informed consent process ensuring that consent is appropriately completed

Prepare and manage source documents according to standard operating procedures

Recognize deviations to the protocol and will work with leadership and staff to address corrective actions to prevent deviations

Assist data coordinator team with case report form completion and query resolution

Work with the Principal Investigator to complete and submit Serious Adverse Event reports

Perform protocol specific closeout related activities in conjunction with the data coordinator

Provide documentation for all deviations whether related to the protocol or a SOP

Ensure that all team members involved understand and adhere to assigned protocols

Other duties may be assigned at any time

Preferred

Experience working in an oncology setting

Benefits

401(k) retirement savings plan with employer match

Eligibility for an annual performance bonus, based on role and company results

Generous paid time off and paid holidays

Comprehensive medical, dental, and vision coverage and optional insurance options

Company paid life and disability insurance for added financial protection

Employee Assistance Program (EAP) providing confidential, no-cost support for you and your family from day one

Flexible FSA and HSA plans to support your financial wellness

Commitment to a supportive environment that values balance, wellbeing, and flexibility

A collaborative, creative workplace where every team member is encouraged to contribute

Continuous learning and professional growth

A culture built on inclusivity and innovation

The START Center for Cancer Research is a oncology and biotechnology research company.

San Antonio, Texas, USA

https://startresearch.com

Late Stage

Total Funding

unknown

2024-04-03

Acquired

Leadership Team

Chris Takimoto

Global Chief Medical Officer

Recent News

PR Newswire

Allegheny Health Network and The START Center for Cancer Research Announce Strategic Collaboration to Expand Patient Access to Early-Phase Cancer Trials

2026-08-25

Bizjournals.com Feed (2025-11-12 15:43:17)

AHN teams up with START Center to expand early-phase oncology research in western Pennsylvania

Baptist Health South Florida and The START Center for Cancer Research Announce Strategic Partnership to Expand Patient Access to Early-Phase Cancer Trials

2026-05-28

Qualifications

High School Diploma or GED

2 years of clinical research experience

Basic understanding of oncology clinical trials, particularly Phase 1 studies

Strong attention to detail and accuracy in data collection and documentation

Ability to manage multiple tasks and meet deadlines in a fast-paced environment

Excellent organizational and time-management skills

Strong communication skills, both written and verbal

Ability to interact professionally with patients, study staff, and external stakeholders

Working knowledge of GCP and regulatory requirements

Proficient in Microsoft Office Suite and clinical trial management software

Experience working in an oncology setting

2 years of clinical research experience.

Required skills

Clinical Research, Oncology Clinical Trials, Phase 1 Clinical Trials, Clinical Practice (GCP), Clinical Research Regulatory Requirements, Microsoft Office Suite

Preferred skills

Experience working in an oncology setting

Experience

2+ years