Senior Oncology CRA: Lead Site Monitoring & Study Delivery
PAREXEL
Parexel is seeking a Senior Clinical Research Associate (SrCRA) to manage the delivery of studies at allocated sites in Indianapolis, Indiana. The SrCRA will collaborate with other CRAs and the Local Study Team to ensure compliance with regulations and quality standards, while also serving as the main contact with study sites. Key responsibilities include monitoring study conduct, training site staff, and ensuring timely documentation. The role requires 5+ years of CRA experience, preferably in Oncology, and a Bachelor’s degree. #J-18808-Ljbffr
- ...Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to oversee site management and monitoring of clinical trials in Indianapolis, Indiana. Responsibilities include... ...of monitoring experience, preferably in Oncology, and a Bachelor’s degree in life sciences....SeniorWebsite
$71.9k - $119.9k
...A leading clinical research organization is hiring a Clinical Research Associate I (CRA I) in Indianapolis, Indiana. This role involves site monitoring, compliance assurance, and close communication with investigative sites. Candidates should have a Bachelor’s degree and...Website$87.2k - $145.3k
...IQVIA Argentina is seeking a CRA 2 based in Indianapolis, United States, with a minimum of 1.5 years of on-site oncology monitoring experience. This role involves performing site monitoring visits, managing study progress, and ensuring regulatory compliance. Candidates...Website- ...IQVIA is hiring a Clinical Research Associate (CRA) in Indianapolis, Indiana. As a CRA, you'll lead site monitoring visits and ensure high-quality execution of clinical trials. You'll be pivotal in driving performance and maintaining compliance. The ideal candidate has...SeniorWebsite
$101.6k - $169.3k
...A leading global clinical research firm is hiring a Senior Clinical Research Associate 1 in Indianapolis. This role involves monitoring and managing clinical study sites, ensuring adherence to protocols and regulations while supporting subject recruitment. Applicants should...SeniorWebsite- ...A leading clinical research organization is seeking a Senior Clinical Research Associate in the Midwest. This role involves monitoring clinical trial sites, ensuring adherence to protocols,... ...sciences and extensive CRA experience, particularly in oncology monitoring, along...SeniorWebsite
- ...Senior Medical Director, Clinical Development (Medical Monitoring) About the Company Rapidly growing organization in the oncology & hematology industry Industry Hospital... ...for assigned studies, acting as the key medical... ...for investigative sites and sponsors, and...SeniorWebsite
- ...Sr CRA Northern VA oncology ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud... ...What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and...SeniorWebsiteFlexible hours
$66.8k - $120k
...Scientific in Indianapolis is hiring a Clinical Research Associate (Level II) to support pharmaceutical companies in clinical monitoring and site management. This position involves on-site and remote monitoring and ensuring compliance with regulatory standards....WebsiteRemote work- ...seeking a Clinical Research Associate (CRA) in Indianapolis, Indiana. The CRA will... ...responsible for managing local clinical studies, monitoring study conduct, and ensuring compliance with... ...involves extensive collaboration with sites and internal teams to ensure study commitments...SeniorWebsiteLocal area
$87.2k - $169.3k
...IQVIA Biotech is seeking Sr. CRA 1 candidates with a minimum of 2 years of on-site monitoring experience in oncology. IQVIA Biotech is a full-... ...sites are conducting the study(ies) and reporting study data... ...company training. IQVIA is a leading global provider of clinical...SeniorWebsiteFull timePart timeLocal areaImmediate startWorldwide$65.25k - $169.4k
...Eli Lilly and Company is seeking an expert Toxicology Study Monitor in Indianapolis, Indiana. The role involves monitoring study conduct at third-party organizations and ensuring compliance with timelines and GLP expectations. Candidates should possess a BS in a relevant...Senior$198k - $389.4k
...primary objective for our Senior Director (Medical Monitor) is to provide input into the... ...and/or generating key study documents (such as medical... ...contributing to investigator, other site staff and clinical study... ...safety plans for studies. Leading and/or participating in scientific...SeniorWebsiteFull timeFlexible hours$90.2k - $175.1k
...Research Associate (CRA) to join our team and... ...partner with investigative sites and cross-functional teams to ensure studies are executed with... ...What You'll Do Lead and execute site monitoring visits (selection, initiation... ...successful study delivery What You Bring ~...SeniorWebsiteFull timePart timeImmediate startWorldwide- ...is responsible for supporting monitoring and site management activities for the client Sponsored studies. Site monitoring and site management... ...Clinical Research Associate (CRA) and Investigator Site... ...years of related experience for Senior CRA. Strong analytical problem...SeniorWebsiteInterim roleWork at officeLocal areaRemote work
- ...Job Purpose The Senior Clinical... ...Associate (Sr. CRA) is responsible for the site management, site monitoring and close‑out... ...safety and quality study execution in... ...ensure effective delivery of clinical... ...preferably 2 years in Oncology) in a CRO or... ..., drive / lead and work...SeniorWebsiteLocal areaRemote work
- ...Parexel FSP is looking for a CRA/Sr CRA in the US. Oncology Experience required. Cell therapy... ...local responsibility for the delivery of the studies at allocated sites and is an active participant... ...and has the responsibility for monitoring the study conduct to ensure proper...SeniorWebsiteLocal areaRemote workFlexible hoursShift work
- ...Job Summary The Senior Clinical Research Associate... ...for the delivery of the studies at allocated sites and is an active participant... ...responsibility for monitoring the study conduct... ...the duties of the CRA with higher proficiency... ...2+ years direct Oncology Monitoring / CRA...SeniorWebsiteLocal areaRemote workFlexible hoursShift work
- ...seeking a Clinical Research Associate (CRA) in Indianapolis, Indiana, to ensure... ...clinical trials. Responsibilities include site management, monitoring, and resolution of protocol-related... ...work closely with site personnel and the study team, conducting site monitoring...Website
- ...candidate will have at least 10 years of field construction experience and 5 years in a superintendent position. This role involves monitoring job site safety, training personnel, and maintaining compliance with OSHA regulations. F.A. Wilhelm provides a competitive salary,...SeniorWebsite
- ...Job Summary: The Senior Manager, Study Start-up partners closely... ...Operations study team leading global study start-up and site activation activities in... ...quality, best in class delivery, acceleration and optimization... ..., study management and monitoring, and local regulatory...SeniorWebsiteLocal areaRemote work
- ...The Senior Study Contract Manager (SrSCM) play an important role in driving the costings and... ...SOPs. · Develop and negotiate clinical site budgets based on Fair Market Value. ·... ...of Clinical Study Management including monitoring, study drug handling and data management...SeniorWebsiteContract workWork experience placementLocal areaRemote workFlexible hoursShift work
- ...Parexel is hiring a Senior Clinical Research Associate located in Indianapolis, Indiana, to oversee site management and monitoring of clinical trials. The role demands a minimum of three years’ experience, ideally in oncology, and includes responsibilities such as ensuring...SeniorWebsite
$87.2k - $145.3k
...| R1537618 IQVIA is seeking a CRA 2 with a minimum of 1.5 years of on-site oncology monitoring experience: Essential Functions... ...Administer protocol and related study training to assigned sites and... ...on-site monitoring. IQVIA is a leading global provider of clinical research...WebsiteFull timePart timeLocal areaImmediate startWorldwide$288.2k - $360.2k
...patient needs in oncology, urology, women's... ...Management (PVRM) Senior Medical Director will... ...(SMP), Clinical Study report (CSR), Investigator... ...Responsibilities Lead safety strategy... ...ongoing safety monitoring of assigned investigational... ..., investigator site training,...SeniorWebsiteWork at officeLocal areaRemote workWorldwideFlexible hours- ...be part of a team that is building the future of agriculture – leading breakthroughs in the innovation and application of science and... ...to announce an exciting opportunity for a Product Chemistry Study Monitor. In this role, you will be responsible for coordinating and executing...Contract workWork experience placementLocal areaShift work
- ...Eli Lilly and Company in Indianapolis is looking for a Senior Director (Medical Monitor) to provide crucial oversight in clinical trials. This role includes reviewing safety data, developing study protocols, and training staff to ensure compliance with regulations. The...Senior
- ...Position: Senior Clinical Research Associate (level... ...Indianapolis, IN Job Id: CRA ongoing IN # of Openings... ...provide an update on a study or milestone that they... ...Manages investigative site activity for multiple protocols... ...pre-study, initiation, monitoring, and close-out) and...SeniorWebsiteLocal areaRemote workWork from homeHome office
- ...sciences and in the support of clinical studies, as well as having an emerging global presence... ...Job Description Collect Environmental Monitoring (EM) and utility samples at client... ...organized manner, and comply with client site requirements At least one year of GMP...WebsiteFull timeContract work
$75k
...the installations and leaving the event site immaculate. We maintain a total commitment... .... The Company is backed by ZMC. ZMC is a leading private equity firm comprised of experienced... ...with project specific plans and layouts Study plans, blueprints, and equipment lists...SeniorWebsiteDaily paidFull timeTemporary workWork at officeShift work
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