Senior CRA - Oncology Trials Lead (Site Monitoring)
Parexel
Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to oversee site management and monitoring of clinical trials in Indianapolis, Indiana. Responsibilities include ensuring patient safety, managing site relationships, and resolving protocol-related issues. Candidates should have at least 3 years of monitoring experience, preferably in Oncology, and a Bachelor’s degree in life sciences. The role requires a proficiency in GCP, the ability to travel up to 80%, and fluency in English. Come join a company committed to excellence! #J-18808-Ljbffr Parexel
- 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... ...of clinical trials. This includes serving... ...contact for investigative sites and sponsors, and...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- Sr CRA Midwest Oncology ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive... ...clinical development. What You Will Be Doing Monitoring clinical trial sites to ensure adherence to study protocols,...SeniorWebsiteFlexible hours
$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... ...available for filing in the Trial Master File (TMF) and verify... ...company training. IQVIA is a leading global provider of clinical...SeniorWebsiteFull timePart timeLocal areaImmediate startWorldwide$87.2k - $169.3k
...Clinical Research Associate (CRA) to join our team and play a... ...high-quality clinical trials. In this role, you’ll partner with investigative sites and cross‑functional teams to... ...patient focus. What You’ll Do Lead and execute site monitoring visits (selection, initiation...SeniorWebsiteFull timePart time$198k - $389.4k
...primary objective for our Senior Director (Medical Monitor) is to provide input into the... ...and conduct of clinical trials, reviewing and/or generating... ...contributing to investigator, other site staff and clinical study... ...safety plans for studies. Leading and/or participating in...SeniorWebsiteFull timeFlexible hours- ...Parexel FSP is looking for a CRA/Sr CRA in the US. Oncology Experience required. Cell... ...the studies at allocated sites and is an active... ...has the responsibility for monitoring the study conduct to ensure... ...delivering quality clinical trials with reduced budget and in...SeniorWebsiteLocal areaRemote workFlexible hoursShift 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
- The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality... ...(preferably 2 years in Oncology). Preferred therapeutic experience...SeniorWebsiteLocal areaRemote work
- Job Summary The Senior Clinical Research Associate... ...at allocated sites and is an active... ...responsibility for monitoring the study conduct... ...the duties of the CRA with higher proficiency... ...quality clinical trials with reduced... ...2+ years direct Oncology Monitoring / CRA experience...SeniorWebsiteLocal areaRemote workFlexible hoursShift work
- Parexel is seeking a Clinical Research Associate (CRA) in Indianapolis, Indiana, to ensure patient safety and quality in clinical trials. Responsibilities include site management, monitoring, and resolution of protocol-related issues. The CRA will work closely with site...Website
- ...Director, Clinical Development Trial Lead (CDTL) independently leads... ...clinical trial successfully. Monitor the status and make adjustments... ...Skills: • Experience with oncology (early & late phase clinical... ...process • Prior clinical trial site-level or affiliate experience...SeniorWebsiteLocal areaRemote work
$87.2k - $145.3k
...IQVIA is seeking a CRA 2 with a minimum of 1.5 years of on‑site oncology monitoring experience: Essential Functions Perform site monitoring visits (selection... ...) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator...WebsiteFull timePart timeLocal area- ...implementation of one or more clinical trials and all activities from study... ..., and operational aspects of site investigator grants and grant... ...Trial Operational Delivery Leads and/or supports clinical... ...related materials such as Clinical Monitoring Plans, Data Management Plans,...SeniorWebsiteContract workRemote work
- ...Position: Senior Clinical Research Associate (level... ...Indianapolis, IN Job Id: CRA ongoing IN # of Openings... ...Manages investigative site activity for multiple protocols... ...pre-study, initiation, monitoring, and close-out) and... ...product(s) and trial-related material. Maintains...SeniorWebsiteLocal areaRemote workWork from homeHome office
$101.6k - $169.3k
IQVIA is hiring Senior Clinical Research Associate... ...experience in either oncology, cardiovascular, renal... ...Job Overview Perform monitoring and site management work to ensure... ...available for filing in the Trial Master File (TMF) and... ...training. IQVIA is a leading global provider of...SeniorWebsiteFull timePart timeLocal areaImmediate startWorldwide- Community Health Network in Indianapolis is seeking a Research Regulatory Coordinator. The role involves leading regulatory activities for clinical trials, ensuring compliance with institutional policies and regulations. Candidates should have at least 3 years of research...Senior
- Cytel is seeking an experienced Principal Biostatistician to lead statistical activities for clinical trials. You will be responsible for overseeing trial processes and leveraging SAS and R programming to analyze data, while also providing guidance to junior statisticians...Senior
$50k - $109.24k
...Job Overview As a Lead Research Clinical Coordinator, you will play... ...aspects of study startups, site initiation, budgeting, IRB submissions... ...terminology and clinical trial processes Experience in... ...Specialty Cardiology Gastroenterology Oncology Schedule 8 hour shift Ability...WebsiteFull timeRelocationShift work- ...Front Desk Monitor Sagebriar at Del Webb is an exciting new master-planned adult community in beautiful Greenwood, IN. Sagebriar is... ...Responsibilities: Provides direct receptionist support to all on-site property needs by providing the highest quality customer service...WebsiteImmediate start
- Eli Lilly and Company is seeking a Senior Engineer for Intralogistics System Integration... ...This mid-level engineering role involves leading project management and technical oversight... ...crucial systems across Lilly’s manufacturing sites. This role requires a Bachelor’s degree...SeniorWebsite
- ...Patient Safety team as a Senior Physician where you'll... ...patients in clinical trials and post-marketing settings... ...provide expert safety monitoring, and deliver... ...Assisting the Project Lead/Functional Lead for audits... ...support to Parexel staff or site (investigator/study coordinator...SeniorWebsiteInternshipWork at officeLocal areaRemote workWork from homeFlexible hours
- ...you will feel valued, have room for advancement, and be rewarded for your good work. We are currently looking for a Pool Monitor to join our on-site community team to help support a positive experience for our residents. Responsibilities Keep residents safe and happy...WebsiteLocal areaWeekend workAfternoon shift
- A leading engineering services firm seeks a Senior Managing Accident Reconstructionist to lead a team in vehicular accident investigations. The ideal candidate... .... Responsibilities include traveling to accident sites, utilizing specialized software for analysis, and providing...SeniorWebsiteRemote jobFlexible hours
- Ericsson GmbH in Indianapolis is looking for a Senior Construction Manager to lead the deployment of telecommunications equipment. You will manage activities... ...include budget oversight, coordinating rollouts, and site feasibility assessments. Join a diverse team that values...SeniorWebsite
- A technology solutions provider is seeking a Senior Configuration Management Analyst with ServiceNow expertise to manage the configuration... ...relevant experience in configuration management. This is an on-site position located in Indiana. Competitive salary and...SeniorWebsite
- Ericsson is searching for a Senior Construction Manager in Indianapolis to lead technical topics within a telecommunications implementation organization. This... ...experience. Strong leadership skills and knowledge of site design consulting are essential. Comprehensive...SeniorWebsite
- Cornerstone Engineering Inc is seeking a Senior Civil Engineer to take a leadership role in civil engineering projects, including site development and infrastructure. This position requires extensive experience, a PE license, and proficiency in AutoCAD and Civil 3D. The...SeniorWebsite
- American Structurepoint, Inc is looking for a Senior Interior Designer in Indianapolis, IN. This role involves leading interior design efforts from concept through design... ...like Revit and SketchUp. This position is on-site and offers opportunities for professional growth...SeniorWebsite
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