Clinical Research Coordinator

The START Center for Cancer Research · Hyde Park, NY · 2 wk ago

On-siteAnalyst$45–$60/hrFull-time

About the role

The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. We are currently hiring a Clinical Research Coordinator to support the daily activities of early phase oncology clinical trials.

Responsibilities

Communicate on a regular basis with Study Sponsor’s, CRO’s, staff, etc. regarding questions, concerns, as well as status of the protocol.
Maintain files using standardized study document labeling and filing procedures.
Create/review forms created or revised for assigned trials to assure protocol compliance.
Implement initial protocol and amendments, training staff who will be involved in patient treatment and management.
Maintain an up-to-date contact list.
Absorb patient screening and determine 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 work with leadership and staff to address corrective actions to prevent deviations.
Aid 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.

Requirements

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.

Qualifications

Experience working in an oncology setting.

Skills

Strong communication skills.
Attention to detail.
Time management.
Knowledge of GCP and regulatory requirements.
Proficiency in Microsoft Office Suite and clinical trial management software.

Benefits

We offer a competitive compensation package, including a range of $45/hour - $60/hour annually, based on experience. Our best-in-class benefits and perks include:

401(k) retirement savings plan with employer match.
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.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.