Clinical Research Coordinator

The START Center for Cancer Research; Pittsburgh (Allegheny County); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

401(k) match

Annual bonus

Paid time off

Medical, dental, vision coverage

Life and disability insurance

EAP

FSA/HSA

Inclusive culture

Job summary

The START Center for Cancer Research in Pittsburgh is seeking a Clinical Research Coordinator to support early-phase oncology trials under supervision of senior staff. You will conduct daily trial activities, ensure protocol compliance, and maintain patient safety and data integrity.

You will screen patients, obtain informed consent, manage source documents, coordinate visits, and communicate with sponsors and CROs.

Qualifications

• High School Diploma or GED.
• 2 years of clinical research experience supporting interventional studies.
• Experience in oncology clinical trials, particularly Phase 1.
• Attention to detail and accuracy in data collection and documentation.
• Ability to manage multiple tasks and meet deadlines in a fast-paced environment.
• Working knowledge of GCP and regulatory requirements.
• Proficient in Microsoft Office Suite and clinical trial management software.

Responsibilities

• Communicate on a regular basis with Study Sponsors, 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, SOPs, and GCP to ensure integrity regarding all aspects of the study.
• Create/review forms created or revised for assigned trials to assure protocol compliance.
• 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 work with leadership and staff to address corrective actions to prevent deviations.
• 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.

Skills

Attention to detail

Multitasking

GCP knowledge

Regulatory knowledge

Communication skills

Education

High School Diploma or GED

Tools

Microsoft Office Suite

Clinical trial management software

Job description

The START Center for Cancer Research (\"START\") is the world's largestearly phasesite network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering \"Hope Through Access\" to cutting edge trials throughout the United States and Europe.

We are currently hiring a Clinical Research Coordinator for our START Pittsburgh site. The Clinical Research Coordinator (CRC) will work under the guidance of senior research staff to support the daily activities of early phase oncology clinical trials. The CRC ensures the accurate and timely conduct of clinical research, adhering to protocols, regulatory requirements, and patient safety standards. This role involves direct patient interaction, data collection, and maintaining compliance with Good Clinical Practice (GCP). The Clinical Research Coordinator will be assigned multiple protocols at any time for which they will oversee the aspects of assigned protocols with planning and coordinating patient participation in the trial.

Work Schedule: Monday-Friday, 8:00am-5:00pm

Location: START - Pittsburgh (320 East North Avenue, Pittsburgh, PA 15212)

Essential Responsibilities:

• Communicate on a regular basis with Study Sponsors, 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.


• 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.


• 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.

Required Education and Experience:

• High School Diploma or GED.


• 2 years of clinical research experience supporting interventional studies


• Strong experience 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.


• Working knowledge of GCP and regulatory requirements.


• Proficient in Microsoft Office Suite and clinical trial management software.

Best-in-Class Benefits and Perks:

• 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 coverageand optional insuranceoptions


• 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


• We’re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you’ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.

More About START:

START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world's largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of \"Hope Through Access\".

Learn more at STARTresearch.com.

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.