RN, Clinical Research Coordinator

The START Center for Cancer Research; Myrtle Beach (SC); On-site; USD 55,000 - 85,000; Full time

Benefits offered by this job

Comprehensive health coverage

401(k) retirement plan with employer-m

Life and disability insurance

Paid time off

Job summary

The START Center for Cancer Research in Myrtle Beach, SC, seeks a Clinical Research Coordinator, RN to support daily activities of early and late-phase oncology and urology trials. You will work under senior staff to ensure protocol adherence, data collection, and patient safety, with direct patient interaction.

Responsibilities include protocol management, consent facilitation, data entry, and cross-functional communication.

Qualifications

• Associate degree in Nursing required; RN license in state practicing.
• Clinical research experience strongly preferred but not required.
• 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.

Responsibilities

• Communicate regularly with Study Sponsors, CROs, staff regarding questions and protocol status.
• Monitor day-to-day conduct of assigned studies per protocol, SOPs, and GCP.
• Create or revise forms for assigned trials to assure protocol compliance.
• Maintain files using standardized study document labeling and filing procedures.
• Implement initial protocol and amendments, training staff involved in patient treatment.
• Maintain an up-to-date contact list and assist with patient screening and eligibility.
• Facilitate informed consent process and ensure proper completion.
• Prepare and manage source documents per SOPs.
• Address deviations with leadership and staff and implement corrective actions.
• Assist data coordinator team with case report form completion and query resolution.
• Collaborate with Principal Investigator to complete SAE reports.
• Perform protocol closeout activities with data coordination.
• Provide documentation for all deviations to SOPs and protocol.
• Ensure team adherence to assigned protocols and procedures.
• Perform telephone triage assessments of patients on trial when necessary.
• Provide patient education regarding participation in trials and potential side effects.

Skills

Attention to detail

Data collection

Time management

Communication skills

GCP & regulatory knowledge

Microsoft Office

Clinical trial management software

Education

Associate’s degree in Nursing

Bachelor’s degree in Nursing

Tools

Clinical trial management software

Microsoft Office Suite

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 Sponsors, CROs, 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.
• Other duties may be assigned at any time.

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 our employees’ time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

• Comprehensive health coverage: Medical, dental, and vision insurance provided
• Robust retirement planning: 401(k) plan available with employer matching
• Financial security: Life and disability insurance for added protection
• Flexible financial options: Health savings and flexible spending accounts offered
• Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
• Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

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.

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.