Clinical Research Site Director
Apply NowCompany: C-Clinical at Century City
Location: Los Angeles, CA 90011
Description:
Description
Exciting Opportunity: Clinical Research Site Director - Lead Cutting-Edge Cancer Research!
We are seeking a motivated and skilled Clinical Research Site Director to oversee the daily operations of our hematology/oncology clinical research site in Los Angeles, CA. This is an incredible opportunity to be at the forefront of groundbreaking cancer research, ensuring the successful execution of clinical drug studies while contributing to advancements in the treatment of hematology and oncology.
As Site Director, you will take charge of managing and leading the site team, collaborating with research sponsors, and ensuring compliance with regulatory standards, including FDA / 21 CFR and ICH-GCP. You'll have the chance to make a significant impact while ensuring the smooth execution of clinical trials and the highest standards of patient care.
We're looking for an experienced and dynamic leader with a deep understanding of clinical research protocols and a solid background in hematology/oncology. If you have the proven ability to manage large teams and are passionate about advancing cancer research, this is your chance to thrive in an essential and rewarding role.
Key Responsibilities:
Ready to take your career to the next level while making a real difference in the world of cancer research? Apply today and join us in advancing the future of oncology!
Responsibilities
Site Management: Oversee daily operations of the clinical research site, including study planning, protocol implementation, patient recruitment, data collection, and maintaining regulatory compliance.
Team Leadership: Manage and mentor a team of approximately 15 Clinical Research Coordinators and 10+ Research Assistants. Provide guidance and training and conduct performance evaluations to ensure high-quality work and adherence to compliance standards.
Regulatory Compliance: Ensure all clinical research activities comply with Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and other relevant regulatory requirements.
Study Execution: Serve as the subject matter expert for sponsors and research organizations, collaborating with the Principal Investigator (PI) to oversee compliance of clinical trial teams in accordance with protocols, timelines, and budgets.
Patient Recruitment & Retention: Work closely with the recruitment team to develop effective strategies for research participant recruitment and retention, ensuring access to eligible participants and maintaining participant engagement throughout the study.
Budget & Financial Oversight: Manage study budgets, invoicing, and site expenditures, ensuring effective use of resources while staying within allocated financial parameters.
Quality Assurance: Ensure data integrity by reviewing audit trails, identifying compliance or quality concerns, and implementing corrective actions. Monitor ongoing site performance to detect risks and take proactive measures.
Collaboration & Communication: Foster strong communication and collaboration between internal teams, study sponsors, and external stakeholders, ensuring alignment and transparency in the study's progress.
Clinical Data Management: Oversee the collection and review of clinical data, ensuring strict compliance with study protocols and regulatory requirements.
Qualifications
Education: Bachelor's degree in life sciences, nursing, or a related field (required). A Master's degree or higher is preferred.
Experience: Minimum of 5 years of clinical research experience, with at least 2 years in hematology/oncology clinical trials. A minimum of 3 years in a management or leadership role overseeing clinical research teams (CRCs and RAs).
Certifications: CCRP (Certified Clinical Research Professional), CCRC (Certified Clinical Research Coordinator), or other relevant certifications preferred.
Knowledge: In-depth understanding of clinical research methodologies, regulatory compliance (FDA, ICH-GCP), and hematology/oncology drug development.
Skills: Strong leadership, communication, organizational, and problem-solving skills. Proficiency in clinical trial management systems and Microsoft Office Suite.
Other: Ability to manage multiple priorities in a fast-paced environment while maintaining high standards of performance and patient care.
Compensation: The salary for this position is competitive and positioned within the 80th to 90th percentile for Clinical Research Site Directors in the Los Angeles area, based on experience and qualifications. A comprehensive benefits package is included, covering health, dental, and vision insurance, 401(k), and paid time off.
Work Environment:
The Clinical Research Site Director will primarily work in a clinical research setting, interacting with patients, site staff, and external stakeholders.
Occasional travel to sponsor meetings or other clinical sites may be required.
Full-time position with flexible hours based on study needs.
Exciting Opportunity: Clinical Research Site Director - Lead Cutting-Edge Cancer Research!
We are seeking a motivated and skilled Clinical Research Site Director to oversee the daily operations of our hematology/oncology clinical research site in Los Angeles, CA. This is an incredible opportunity to be at the forefront of groundbreaking cancer research, ensuring the successful execution of clinical drug studies while contributing to advancements in the treatment of hematology and oncology.
As Site Director, you will take charge of managing and leading the site team, collaborating with research sponsors, and ensuring compliance with regulatory standards, including FDA / 21 CFR and ICH-GCP. You'll have the chance to make a significant impact while ensuring the smooth execution of clinical trials and the highest standards of patient care.
We're looking for an experienced and dynamic leader with a deep understanding of clinical research protocols and a solid background in hematology/oncology. If you have the proven ability to manage large teams and are passionate about advancing cancer research, this is your chance to thrive in an essential and rewarding role.
Key Responsibilities:
- Lead and manage site staff
- Collaborate with research sponsors to ensure study success
- Ensure compliance with all regulatory guidelines and industry standards
- Maintain a high standard of care for research participants
- Oversee study timelines and operational effectiveness
Ready to take your career to the next level while making a real difference in the world of cancer research? Apply today and join us in advancing the future of oncology!
Responsibilities
Site Management: Oversee daily operations of the clinical research site, including study planning, protocol implementation, patient recruitment, data collection, and maintaining regulatory compliance.
Team Leadership: Manage and mentor a team of approximately 15 Clinical Research Coordinators and 10+ Research Assistants. Provide guidance and training and conduct performance evaluations to ensure high-quality work and adherence to compliance standards.
Regulatory Compliance: Ensure all clinical research activities comply with Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and other relevant regulatory requirements.
Study Execution: Serve as the subject matter expert for sponsors and research organizations, collaborating with the Principal Investigator (PI) to oversee compliance of clinical trial teams in accordance with protocols, timelines, and budgets.
Patient Recruitment & Retention: Work closely with the recruitment team to develop effective strategies for research participant recruitment and retention, ensuring access to eligible participants and maintaining participant engagement throughout the study.
Budget & Financial Oversight: Manage study budgets, invoicing, and site expenditures, ensuring effective use of resources while staying within allocated financial parameters.
Quality Assurance: Ensure data integrity by reviewing audit trails, identifying compliance or quality concerns, and implementing corrective actions. Monitor ongoing site performance to detect risks and take proactive measures.
Collaboration & Communication: Foster strong communication and collaboration between internal teams, study sponsors, and external stakeholders, ensuring alignment and transparency in the study's progress.
Clinical Data Management: Oversee the collection and review of clinical data, ensuring strict compliance with study protocols and regulatory requirements.
Qualifications
Education: Bachelor's degree in life sciences, nursing, or a related field (required). A Master's degree or higher is preferred.
Experience: Minimum of 5 years of clinical research experience, with at least 2 years in hematology/oncology clinical trials. A minimum of 3 years in a management or leadership role overseeing clinical research teams (CRCs and RAs).
Certifications: CCRP (Certified Clinical Research Professional), CCRC (Certified Clinical Research Coordinator), or other relevant certifications preferred.
Knowledge: In-depth understanding of clinical research methodologies, regulatory compliance (FDA, ICH-GCP), and hematology/oncology drug development.
Skills: Strong leadership, communication, organizational, and problem-solving skills. Proficiency in clinical trial management systems and Microsoft Office Suite.
Other: Ability to manage multiple priorities in a fast-paced environment while maintaining high standards of performance and patient care.
Compensation: The salary for this position is competitive and positioned within the 80th to 90th percentile for Clinical Research Site Directors in the Los Angeles area, based on experience and qualifications. A comprehensive benefits package is included, covering health, dental, and vision insurance, 401(k), and paid time off.
Work Environment:
The Clinical Research Site Director will primarily work in a clinical research setting, interacting with patients, site staff, and external stakeholders.
Occasional travel to sponsor meetings or other clinical sites may be required.
Full-time position with flexible hours based on study needs.