Wait…
The role
Job Summary
We are seeking a highly experienced Manager, Clinical Research (Oncology) with a minimum of 5 years of experience in clinical trials regulatory management. The ideal candidate will have worked in either a pharmaceutical firm and a clinical research organization (CRO) and have hands-on experience with investigative studies and clinical trials.
\
Job Description
The Manager for Clinical Research (Oncology) will be responsible for overseeing the spectrum of activities for clinical trials in our research division. This role will involve providing independent regulatory support for complex projects and programs. The ideal candidate will demonstrate a strong understanding of clinical research regulations and possess comprehensive regulatory expertise.
- Take a lead role in the planning and execution of clinical trials, ensuring adherence to timelines, budgets, and quality standards
- Develop and oversee study scope of work, budgets and timelines
Develop and maintain study documents, such as SDC, protocols, informed consent forms, and study manuals, in accordance with company and regulatory standardsFacilitate the initiation of new studies, including completion and accurate submission of all amendments to the PRMC (protocol review and monitoring committee), Institutional Review Board (IRB), adhering to regulatory guidelines and protocolsManage and oversee the day-to-day operations of assigned clinical trials, including monitoring progress, identifying and resolving issues, and ensuring compliance with regulationsCollaborate with cross-functional teams, including study managers, data managers, and medical professionals, to ensure successful study outcomesCommunicate with external partners, such as investigative sites, co-sponsors, and vendors, to establish and maintain effective relationshipsMonitor and track study progress, maintain CTMS, EDC, regulatory bindersProviding regular updates and reports to senior management and stakeholdersParticipate in the selection and management of investigative sites, ensuring they have the necessary resources and training to conduct the studyEnsure compliance with company policies, standard operating procedures, and regulatory requirementsIdentify areas for process improvement and implement solutions to increase efficiency and effectivenessMentor and provide guidance to team members on best practices and industry standardsStay current with industry trends and developments, and apply knowledge to enhance study processes and outcomesRepresent the company at conferences and meetings, promoting the organization's mission and valuesMaintain confidentiality of all sensitive information and adhere to ethical standardsLocation: Houston, USA
Position: Mid-career/Senior
Minimum Required Education and Experience
- Education: Degree in life science-related discipline or professional equivalent.
- Experience:
o At least 5 years of relevant experience in clinical trials regulatory management.
o Experience working in research division of pharmaceutical firm or a clinical research organization (CRO) is required.
o Experience with investigative studies and clinical trials is strongly preferred.
o Supervisory experience in managing personnel or processes for regulatory affairs within a research organization is strongly preferred.
o RAC, SOCRA, or equivalent certification is required and must be maintained throughout duration of employment.
o GCP training certification/recertification within 2 years is required
\
o Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
o Extensive use of keyboard requiring repetitive motion of fingers.
o Regular sitting for extended periods.
o Travel may be required.
About Ankr Health
Ankr Health is a US-based company with offices in San Francisco, Houston, and Bangalore. We create transformative technologies for clinics and hospitals to improve patient outcomes. Our flagship platform is the # 1 side effect management solution for oncology and surgery.
Ankr also has an industry-first, generative AI-powered virtual clinics-as-a-service platform. Learn more at https://ankrhealth.com
Similar jobs at other companies

Arrowhead Pharmaceuticals San Diego, California +1
$125K–$135K / yr
Posted 20 days ago
- ET
$304K–$368K / yr
Posted Jul 21, 2026

CareDx, Inc.Brisbane, CA +1
$100K–$130K / yr
Posted 6 days ago
- PF
Pay not posted
Posted Aug 4, 2026

Pay not posted
Posted Aug 4, 2026
- ET
Eikon TherapeuticsJersey City, NJ +1
$270K–$326K / yr
Posted Aug 27, 2026
Source: the Y Combinator job board. We last checked this job 3 days ago. We first saw it 3 days ago. A job on a job board does not always mean that the team interviews people now.