Clinical Trial Manager
Alpha-9 Oncology
Alpha-9 Oncology is seeking a highly motivated Clinical Operations Manager with a strong background in oncology clinical trials and vendor management to support the day-to-day execution of radiopharmaceutical studies. In this role, you will ensure clinical activities are conducted in alignment with protocols, applicable regulations, and company SOPs while partnering closely with the Clinical Operations Leader, who provides overall study strategy and accountability for trial delivery. This is a hands-on role for someone who enjoys solving problems, coordinating across teams and vendors, and driving progress in a fast-paced clinical environment. You will play a key role in translating study strategy into effective execution and helping advance therapies that impact patients. This role reports to the Clinical Operations Leader. How You’ll Contribute Support tracking of clinical trial timelines, budgets, key operational metrics, and study risks, including site activation, enrollment progress, and monitoring issues. Support the CRO/vendor selection strategy and development of operational strategies including country & site selection. Contribute to the development of site feasibility questionnaires and analysis of the feasibility results. Manage day-to-day relationships with clinical trial vendors, including tracking vendor contracts, budgets, invoices, and payments against contracted scope of work, and escalating issues or variances to Clinical Operations leadership. Provide operational input into the development of clinical protocols, informed consent, study manuals, study reports, eCRF and other key operational/regulatory documents. Collaborate with cross-functional teams including Data Management, Clinical Sciences, and Clinical Development to support study execution and resolution of operational issues. Review study site monitoring reports in alignment with the CRO oversight plan. Responsible for maintaining internal study documents in the Trial Master File (TMF) and periodically reviewing the CRO TMF for completeness and accuracy. Support forecasting and management of clinical trial supplies (e.g., lab kits) to ensure sites have the materials needed to conduct studies. Assist in the preparation of Investigator and Study Coordinator Meetings. Ensure study adherence to regulatory requirements (ICH, FDA, EMA, etc.) and ICH/GCP guidelines and SOPs. Provide input to the drafting of governance documents, SOPs, work instructions, and other resources. The Skills You Bring Bachelor’s degree in Life Sciences or a related field; advanced degree preferred, with 3-5 years of experience in clinical operations within the pharmaceutical or biotechnology industry. Working knowledge of ICH/GCP regulations. Experience with early-stage oncology trials required; radiopharmaceutical experience preferred. Strong organization skills and keen attention to detail. Excellent writing and communication skills. Proven ability to proactively identify and resolve issues and ability to work independently on operational assignments. Willingness to roll up your sleeves and get the job done. Strong interpersonal skills with the ability to interact effectively with all levels of associates both within and outside the organization. What's In It For You: At Alpha-9 Oncology, we offer a competitive and comprehensive benefits package designed to support all employees. Our benefits include a competitive salary, bonus, equity, 20 vacation days, 5 sick days, a technology allowance, and commuter reimbursement. We also provide generous retirement savings plans with employer matching, extended health benefits, and paid holidays, tailored to local standards in each region. While specific offerings may vary by location, our commitment to fostering a supportive and rewarding work environment is consistent across the company. Company Summary Alpha-9 Oncology is a clinical-stage biotechnology company pioneering radiopharmaceutical innovation for solid tumors. Our proprietary scaffolds, composed of optimized binders, linkers, chelators, and radioisotopes, enable targeted radiation delivery to cancer cells, minimizing harm to surrounding healthy tissue. Focusing on innovative targeting moieties, we develop molecules tailored for precise tumor targeting. Our comprehensive platform integrates imaging and therapeutic studies to ensure effective radiation delivery and improved patient outcomes. With a robust pipeline entering clinical trials and strong support from leading healthcare investors, Alpha-9 is positioned for rapid growth and advancement in cancer therapy. More About Alpha-9 Oncology Alpha-9 Oncology is committed to fostering a diverse and inclusive workplace and is proud to be an Equal Opportunity Employer. We provide employment opportunities to all qualified applicants without regard to race, ethnicity, religion, age, sex, gender identity or expression, sexual orientation, disability, marital status, family status, national origin, or any other characteristic protected by applicable federal, provincial, or local laws where we operate. We are dedicated to providing reasonable accommodations to qualified applicants and employees to ensure that everyone can perform their essential job functions in an inclusive environment. For inquiries regarding accommodations in the hiring process or for current employees, please contact a member from our Talent Acquisition team. #J-18808-Ljbffr Alpha-9 Oncology
$115k - $200k
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...talented individuals with diverse backgrounds, cultures, perspectives, and experiences to join our team. What You’ll Do The Clinical Trial Manager will provide project support to team members by leading and/or participating in the daily management of clinical trial...Full timeWork experience placementWork at officeLocal areaFlexible hours3 days per week$140k - $168k
...Annually PROMETRIKA is a full-service clinical research organization (CRO) with extensive... ...experience in clinical operations, data management, biostatistics, medical writing, and... ...all sizes. RESPONSIBILITIES The Clinical Trial Manager (CTM) works closely with various...Contract workWork experience placement$88 - $103 per hour
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$160k - $200k
...the desire to work on novel ideas.As the Senior Manager, Patient Support Operations, you will report to the Head of Clinical Operations to serve as the primary "Patient... ...planning, execution, and management of clinical trials in accordance with regulatory requirements and...Temporary workImmediate startRemote work$168k - $188k
...This role will be responsible for project management in the initiation, execution and close out of domestic and international clinical studies, including study concept and design... ...to work within established clinical trial paradigms while exploring and embracing new...Contract workLocal areaRemote work$153k - $197.6k
Senior Clinical Trial Manager We are seeking a Senior Clinical Trial Manager with relevant Clinical Operations experience to join our growing Clinical Development group who will be responsible for providing trial management support for our oncology programs. This role...Work at office$164k - $185k
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- What you\'ll be doing: Lead clinical trials from startup through closeout, owning timelines, budgets, and operational execution Manage CROs, vendors, and investigative sites to ensure high-quality study delivery Partner cross-functionally with Clinical Development, Data...3 days per week
$150k - $180k
Senior Clinical Trial Manager, Clinical Operations Full-Time, Permanent Waltham, MA (at least 2x/month onsite) $150k-$180k with flexibility depending on experience 15% bonus Position Purpose The Sr. Clinical Trial Manager must have experience as a Global Study Lead...Permanent employmentFull timeInterim role- Summary Senior Clinical Trial Manager will lead the day-to-day activities in a clinical trial, and support the program strategy in a highly collaborative environment. The successful candidate will manage members of the clinical operations team, including those at CROs...Contract workRemote work
- ...details Good organizational skills Ability to follow directions Good communication skills Computer literacy Working knowledge of clinical research protocols Ability to demonstrate respect and professionalism for subjects’ rights and individual needs QualificationsEDUCATION...Daily paidRemote work
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$23.13 per hour
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