Clinical Research Coordinator, RN

START Center for Cancer Research; Myrtle Beach (SC); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

401(k) retirement plan with employer x

Annual performance bonus

Paid time off and holidays

Comprehensive medical/dental/vision

Life and disability insurance

Employee Assistance Program (EAP)

Flexible FSA and HSA

Collaborative, inclusive culture

Job summary

The START Center for Cancer Research is seeking a Clinical Research Coordinator, RN to support daily activities of oncology and urology clinical trials in Myrtle Beach. You will oversee protocol adherence, patient interaction, data collection, and GCP compliance.

Responsibilities include sponsor communications, site monitoring, form creation, staff training, patient screening, informed consent, SAE reporting, and closeout activities, while maintaining documentation and meeting deadlines in a

Qualifications

• Associate degree in Nursing required.
• RN license in state practicing.
• Clinical research experience preferred but not required.
• Knowledge of GCP and regulatory requirements.

Responsibilities

• Communicate regularly with Study Sponsors, CROs, staff regarding questions and protocol status.
• Monitor day-to-day conduct of studies per protocol, SOPs, and GCP to ensure integrity.
• Create or revise forms to assure protocol compliance.
• Maintain files with standardized labeling and filing procedures.
• Implement initial protocol and amendments; train staff involved in treatment and management.
• Maintain an up-to-date contact list.
• Assist with patient screening and eligibility determinations.
• Facilitate informed consent process.
• Prepare and manage source documents per SOPs.
• Address deviations with leadership to prevent recurrence.
• Assist data coordinator with CRF completion and query resolution.
• Collaborate with PI to complete SAE reports.
• Perform protocol-specific closeout activities with data coordinator.
• Provide documentation for all deviations; ensure team adherence to protocols.
• Perform telephone triage assessments of trial patients.
• Provide patient education on trial participation and potential side effects.

Skills

RN license

Data collection

Attention to detail

Multitasking

Communication

Education

Associate's degree in Nursing

RN license

Bachelor’s degree in Nursing

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 tooncologyclinical research. Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering "Hope Through Access"tocutting edgetrials throughout the UnitedStatesand Europe.

The Clinical Research Coordinator, RN will work under the guidance of senior research staff to support the daily activities of early and late phase oncology and urology clinical trials. The CRC, RN 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, RN 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. Also, this role is responsible for implementation as well as completion of protocol specific requirements, providing accurate, up to date information to all team members involved with any aspect of carrying out protocol specific requirements.

Work Schedule

Monday-Friday 8:00am-5:00pm

Location

823 82nd Parkway, Suite B, Myrtle Beach, SC, 29572

Essential 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.
• Perform telephone triage assessments of patients on trial when necessary.
• Provide patient education regarding participation in a clinical trial, chemotherapy/biotherapy/investigational agent administration and potential side effects.

Required Education and Experience

• Associate’s degree in Nursing.
• RN license in state practicing.
• Clinical research experience strongly preferred but not required
• Basic understanding of early and late phase oncology and urology clinical trials
• 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.

Preferred Education and Experience

• Bachelor’s degree in Nursing.
• Experience working in an oncology setting.

Physical and Travel Requirements

• Approximately 80% of time is spent sitting.
• Very fast-paced and ever-changing healthcare environment.
• Demanding deadlines and time frames.
• Constant demand for updating knowledge.
• Works closely with physicians and ancillary personnel in caring for and treating oncology/hematology patients.

Best-in-Class Benefits and Perks

We value the time, talent, and dedication our employees bring to START. Our commitment to yourwell-beingand growth is reflected in a competitive compensation package—based on experience—along with comprehensive benefits designed to support you both personally and professionally:

• 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’recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you’lljoin 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. STARTrepresentsthe world’s largest roster of early-phase principal investigators across its Network of clinical trial sites.

Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?

Join us in our mission to conquer cancer, one clinical trial at a time. Yourexpertiseand dedication can help us bring hope and healing to patients worldwide.

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.