Regulatory Coordinator: Cancer Trials Start-up & Compliance
$55.53k - $61.7kDana-Farber Cancer Institute
A leading cancer research organization in Boston seeks a Regulatory Coordinator to prepare and submit protocol applications and maintain compliance with regulatory requirements. The ideal candidate will have a Bachelor’s degree or relevant experience, strong communication skills, and a proficient understanding of medical terminology. This position involves collaboration with various stakeholders, including clinical trial experts and regulatory agencies. A commitment to creating an inclusive environment is essential. The salary range is $55,530.00 - $61,700.00. #J-18808-Ljbffr
$55.53k - $61.7k
A prominent cancer research institution in Boston seeks a Regulatory Coordinator to manage submissions and compliance for clinical research projects. The person will collaborate with various stakeholders including faculty and study team members. Key responsibilities include...Regulatory$55.53k - $61.7k
...The Regulatory Coordinators (RC) works under the direction of the... ...directly for the Clinical Trials Office to complete... ...to ensure regulatory compliance with DFCI and DF/HCC... ...communities, Dana-Farber Cancer Institute is a leader... ...new protocol start-up packet; initiate, facilitate...RegulatoryWork at officeLocal area$48.1k - $54.4k
Dana-Farber Cancer Institute is seeking a Clinical Research Coordinator (CRC) to support clinical trials focused on Breast Oncology. The CRC will... ...manage patient data and ensure compliance with research protocols.... ...trial processes, from start-up to close-out, and requires...Suggested- ...Anesthesiology in Boston is seeking a Clinical Research Associate (CRA I) to support cancer studies. This position manages data collection and regulatory submissions while ensuring that all compliance regulations are followed. The ideal candidate should possess a Bachelor's...Regulatory
$53k - $77k
Boston Medical Center (BMC) is seeking a Clinical Research Regulatory Coordinator to manage regulatory compliance for clinical trials in Boston, MA. The role requires a bachelor's degree in life sciences, nursing, or a related field, and 2-3 years of experience in research...Regulatory- Dana-Farber Cancer Institute is looking for a Clinical Research Coordinator in Boston to oversee clinical trials and manage data compliance within the Multiple Myeloma... ...requires overseeing trial start-up processes, managing... ...adherence to regulatory protocols. The ideal...Regulatory
- ...Regulatory Coordinator The Regulatory Coordinators (RC) works... ...directly for the Clinical Trials Office to complete... ...to ensure regulatory compliance with DFCI and DF/HCC... ...communities, Dana-Farber Cancer Institute is a leader... ...new protocol start-up packet; initiate, facilitate...RegulatoryWork at officeLocal area
$48.1k - $54.4k
A leading cancer research institute in Boston seeks a Clinical Research Coordinator to manage clinical trials and ensure compliance with protocols. This role involves data collection, oversight of trial operations, and interaction with patients. Candidates should have a...- ...functions to implement statistical methodologies and maintain compliance with regulatory requirements. The ideal candidate will have a Ph.D. in... ...strong background in regulatory submissions and innovative trial designs. This is a full-time position offering an opportunity...RegulatoryFull time
$183k - $275k
...aiding rare disease drug development. The role involves leading statistical approaches in clinical trials, managing junior statisticians, and ensuring compliance with regulatory standards. The position is location agnostic, allowing for remote or hybrid work from the...RegulatoryRemote work- ...Clinical Operations Manager/Sr Manager to oversee the planning and execution of clinical trials. This role includes managing timelines and budgets while ensuring compliance with regulatory requirements. The ideal candidate will possess a degree in Life Sciences and...Regulatory
- Beth Israel Lahey Health is seeking a Clinical Trials Monitor (CTM) based in Boston, Massachusetts. The CTM will oversee and... ...clinical research studies across various disease groups, ensuring compliance with regulatory guidelines. This remote position may require occasional on-...RegulatoryRemote jobCasual work
$80k - $105k
...Coordinator, Operations The Coordinator, Operations supports the Integrated Operations team in the delivery of operational excellence, regulatory compliance, and continuous improvement initiatives across Vantage's network. Working collaboratively with internal teams...RegulatoryRemote work- ...Therapeutics in Cambridge, Massachusetts is seeking a Senior Clinical Trial Manager to lead cross-functional teams and ensure successful... ...to conduct global clinical trials while maintaining regulatory compliance. The ideal candidate will have at least 6 years of clinical...RegulatoryFull time
- Eight Sleep is seeking a Senior Clinical Trials Manager to lead the execution of clinical studies, ensuring compliance with regulatory requirements and successful completion of trials. You will work across internal teams and oversee third-party clinical sites, focusing...Regulatory
- Job Summary The Coordinator, Sponsored Research provides support for sponsored research activities... ...documentation, award tracking, and compliance documentation collection. The role... ...applicable. Stay informed of procedural, regulatory, and University updates and system...RegulatoryWork at officeRemote workMonday to Friday3 days per week
- ...Pittsfield, Massachusetts, to handle MDS assessments and coordinate care planning. This critical role ensures compliance with federal and state regulations while... ...to influence resident care positively and meet regulatory standards. #J-18808-Ljbffr TravelNurseSourceRegulatory
- ...patients living with cancers driven by RAS/... ...are exploring regulatory pathways for Europe... ...resistance. With clinical trials underway, we have... ...Operations and Compliance, Senior... ...other functionals to coordinate case management,... ...in a fast-paced, start-up environment and manage...Regulatory
- ...is seeking a Clinical Research Coordinator to support clinical trial operations for a leading pharmaceutical... ...efficiently, ethically, and in compliance with regulatory standards. Key Responsibilities... ...requirements Assist with study start-up, monitoring visits, and close-...Regulatory
- ...responsibilities include coordination of patient scheduling and... ...educational activities, ensuring regulatory and accreditation compliance, participation in the... ...communities, Dana-Farber Cancer Institute is a leader in... ...specified in clinical trials. The IS will oversee any...RegulatoryCasual workMonday to FridayFlexible hoursDay shift
- ..., and management of clinical trials, ensuring successful delivery... ...within budget, while adhering to regulatory requirements and company... ...to the highest standards, in compliance with Good Clinical Practices... ...complex clinical trials from start-up to completion. Experience working...RegulatoryContract work
$62k - $86k
...transformative therapies for cancer and autoimmune... ...1/2 clinical trial across multiple... ...across trial start-up, conduct, maintenance... ...activities in compliance with ICH-GCP, applicable... ...FDA and global regulatory requirements,... ...company SOPs. Coordinate trial activities...RegulatoryTemporary workWork experience placementWork at officeFlexible hours3 days per week- ...surveillance, signal detection, and regulatory reporting. This individual... ...safety activities, ensuring compliance with global pharmacovigilance... ...(ICSR) review for clinical trials and post‑market programs.... ...better life for patients with cancer. AVEO currently markets FOTIVDA...Regulatory3 days per week
- ..., ensuring timely data packages for regulatory submissions in compliance with regulatory standards and aligned... ...necessary to support clinical trials. The ideal candidate is an expert... .... Changing Lives. ARTBIO redefines cancer care by discovering and developing a...RegulatoryContract work
- ...patients living with cancers driven by RAS/MAPK pathway... ....S. and are exploring regulatory pathways for Europe... ...resistance. With clinical trials underway, we have an... ...on contract terms, compliance obligations, and risk... ...efficiency and consistency. Coordinate with Verastem’s...RegulatoryContract work
- Clinical Contract Coordinator II Location: Cambridge, MA Contract: 12+ months - possible... ...programs. This role ensures compliance with regulatory requirements, quality standards, and... ...associated documentation in the electronic Trial Master File (eTMF) Education: Bachelor...RegulatoryContract workLocal area
$163.1k - $186.7k
...A leading cancer research organization in Massachusetts is seeking a Regulatory Compliance Director to oversee compliance programs and ensure adherence to regulations. The ideal candidate will have extensive regulatory expertise and leadership experience, collaborating...RegulatoryFull time$45.5k - $54.4k
...surrounding communities, Dana-Farber Cancer Institute is a leader in cancer research... ...check-in/check-out functions; coordinates complex schedules and entering verbal... ...using standard operating procedures. Regulatory Compliance and Quality Improvement: Ensures compliance...Regulatory$45.5k - $54.4k
...Administrative Coordinator Reporting to the Practice Manager, this mission critical... ...surrounding communities, Dana-Farber Cancer Institute is a leader in life changing... ...using standard operating procedures Regulatory Compliance and Quality Improvement: Compliance...Regulatory$77.4k - $102.8k
Dana-Farber Cancer Institute seeks a Clinical Research Manager to oversee clinical trials in Breast Oncology. Responsibilities include managing research teams, ensuring regulatory compliance, and collaborating with physicians. The ideal candidate will have a Bachelor’s...Regulatory
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