About The Company
The START Center for Cancer Research ("START") is recognized as the world’s largest early phase site network dedicated exclusively to oncology clinical research. With a rich history of advancing cancer treatment, START has been instrumental in providing hope to patients worldwide by offering access to cutting-edge clinical trials across the United States and Europe. Our organization is committed to accelerating the development of innovative therapies through rigorous research and collaboration with leading healthcare professionals. We have conducted over a thousand early-phase clinical trials, including 43 therapies approved by the FDA, demonstrating our leadership and dedication in the field of oncology. Our network encompasses multiple clinical trial sites, each staffed with experienced investigators and research teams focused on delivering impactful results. At START, we prioritize fostering a collaborative, inclusive, and innovative environment where team members can grow professionally while contributing to life-changing advancements in cancer treatment.
About The Role
We are seeking a motivated Clinical Data Entry Coordinator to join our team. In this vital role, you will be responsible for collecting, accurately entering, transcribing, and transmitting clinical data for assigned investigational drug studies. Your work will ensure the integrity and quality of data collected during clinical trials, which is crucial for the success of our research efforts. The position offers an opportunity to contribute directly to groundbreaking cancer research, supporting the collection and management of data that can lead to new therapies and improved patient outcomes. You will collaborate with study teams, monitor data accuracy, and assist in maintaining compliance with protocols and regulatory standards. This role provides a dynamic and engaging environment for individuals passionate about clinical research and data management, with opportunities for professional development and growth within a leading organization in oncology research.
Qualifications
START Center for Cancer Research is an equal opportunity employer that values diversity and inclusion. We are committed to creating a workplace free from discrimination and harassment. We welcome applications from individuals of all backgrounds regardless 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 protected characteristic under federal, state, or local law. We believe that a diverse workforce enhances our ability to innovate and better serve our community and patients worldwide.
The START Center for Cancer Research ("START") is recognized as the world’s largest early phase site network dedicated exclusively to oncology clinical research. With a rich history of advancing cancer treatment, START has been instrumental in providing hope to patients worldwide by offering access to cutting-edge clinical trials across the United States and Europe. Our organization is committed to accelerating the development of innovative therapies through rigorous research and collaboration with leading healthcare professionals. We have conducted over a thousand early-phase clinical trials, including 43 therapies approved by the FDA, demonstrating our leadership and dedication in the field of oncology. Our network encompasses multiple clinical trial sites, each staffed with experienced investigators and research teams focused on delivering impactful results. At START, we prioritize fostering a collaborative, inclusive, and innovative environment where team members can grow professionally while contributing to life-changing advancements in cancer treatment.
About The Role
We are seeking a motivated Clinical Data Entry Coordinator to join our team. In this vital role, you will be responsible for collecting, accurately entering, transcribing, and transmitting clinical data for assigned investigational drug studies. Your work will ensure the integrity and quality of data collected during clinical trials, which is crucial for the success of our research efforts. The position offers an opportunity to contribute directly to groundbreaking cancer research, supporting the collection and management of data that can lead to new therapies and improved patient outcomes. You will collaborate with study teams, monitor data accuracy, and assist in maintaining compliance with protocols and regulatory standards. This role provides a dynamic and engaging environment for individuals passionate about clinical research and data management, with opportunities for professional development and growth within a leading organization in oncology research.
Qualifications
- Bachelor’s degree or equivalent experience in a related field
- Experience working within a clinical research organization (CRO) or similar setting
- Strong attention to detail and organizational skills
- Proficiency in data entry and management, including electronic and paper-based CRFs
- Excellent communication skills for coordinating with study teams and monitor visits
- Ability to review and interpret clinical data for accuracy and completeness
- Knowledge of clinical trial protocols and regulatory requirements
- Experience with lab coordination and understanding of lab certifications (preferred)
- CCR or CCRC credentials are highly desirable
- Collect, transcribe, and transmit clinical data from paper and electronic case report forms (CRFs)
- Ensure timely and accurate entry of clinical data, including correction and query resolution
- Coordinate with the study team to receive patient records and data necessary for CRF completion
- Review patient data for accuracy, completeness, and consistency across assigned studies
- Schedule and facilitate monitor visits, including exit meetings and audits
- Identify laboratory facilities used for studies and communicate with Regulatory Affairs to obtain necessary certifications
- Adhere to study protocols and regulatory guidelines during data management activities
- Maintain current data entry and documentation for all assigned studies
- Attend study-related meetings, including site initiation, monitor exit, and close-out meetings
- Collaborate with accounts receivable staff regarding data submissions and billing processes
- Comprehensive health coverage including medical, dental, and vision insurance
- Retirement plan with employer matching contributions (401(k))
- Life and disability insurance for financial security
- Health savings accounts (HSAs) and flexible spending accounts (FSAs)
- Paid time off and holidays to support work-life balance
- Flexible scheduling options and remote work opportunities
- Professional development and growth opportunities within a leading research organization
- Supportive and collaborative work environment fostering innovation and learning
START Center for Cancer Research is an equal opportunity employer that values diversity and inclusion. We are committed to creating a workplace free from discrimination and harassment. We welcome applications from individuals of all backgrounds regardless 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 protected characteristic under federal, state, or local law. We believe that a diverse workforce enhances our ability to innovate and better serve our community and patients worldwide.