- IQVIA (Durham, NC)
- **IQVIA is seeking a Sr . CRA 1 or CRA 2 with a minimum of 1.5 years of on-site oncology monitoring experience:** _Essential Functions_ Perform site monitoring visits ... drive, and track subject recruitment plan in line with project needs to enhance predictability. Administer protocol and related...the Trial Master File (TMF) and verify that the Investigator 's Site File (ISF) is maintained in accordance with… more
- Chiesi (Milwaukee, WI)
- …identify new collaborative KOL relationships for advisory boards, company-sponsored, investigator -initiated research , and speaker development + Provide beliefs, ... scientific meetings + Provide field-based medical affairs assistance for clinical research initiatives supported by Company, related to Investigator Initiated… more
- Geisinger (Danville, PA)
- …candidate will enjoy 80% protected research time along with dedicated research support staff including project management and biostatistical support. The ... of CKD, cardiovascular-kidney-metabolic syndrome, and patient-centered care. Resources include research data analyst support, project manager, project… more
- Bristol Myers Squibb (San Diego, CA)
- …RayzeBio aims to be the global leader in radiopharmaceuticals . The Senior Medical Director - Clinical Development (GU Cancer/Prostate Renal) has responsibility for ... design a clinical development plan for nominated drug candidates + Lead internal project teams, and partner with investigators and CROs to design and implement… more
- AbbVie (San Francisco, CA)
- …executes and maintains high impact territory plans, including HCP and Investigator engagement plans in alignment with Dermatology medical and scientific objectives ... assigned geography. + Delivers on territory plan objectives, meets assigned project deadlines, and achieves annual functional goals. Generates and documents… more
- Merck (North Wales, PA)
- …skills as part of a global, cross-functional team. You will apply project management, communication, and collaboration skills in support of our clinical trials. ... trial level plans/timelines, country/site selection, site materials, system updates, investigator meeting planning, communication plans, preparation of status update… more
- IQVIA (Overland Park, KS)
- Job Overview: Join our dynamic team as a Clinical Research Associate! You'll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance ... sponsor requirements. Be at the forefront of groundbreaking cancer research and make a real impact on patients' lives....with sites to develop and track recruitment plans, ensuring project needs are met. Training & Communication: Provide protocol… more
- Kelly Services (West Point, PA)
- ** Senior Study Manager I** **Therapeutic Areas: Oncology & Immunology** **Description of Services** May lead or support a study or studies, depending on ... interactions with external vendors (eg, IVRS, PRO) + Initiates planning for Investigator meeting and protocol training. + Plans and assesses protocol ancillary… more
- Gilead Sciences, Inc. (Foster City, CA)
- …VP, Head of MAR. **Key Responsibilities:** + Ensures operational oversight of Investigator Sponsored Research (ISR) and Collaborative studies including but not ... Operations, Medical Affairs, Real World Evidence, Health Economics and Outcomes Research , Project Management, Regulatory, Biometrics, Clinical Research … more
- Avania (OR)
- Avania are hiring for the key role of experienced Clinical Research Associate (CRA) or Senior Clinical Research Associate ( Sr CRA) As a CRA/ Sr CRA ... visits, from site management to sponsor management As a CRA/ Sr CRA you will: + Be responsible for the...during visits. + Organize and actively participate in sponsor, investigator and project meetings. + Provide consistent… more
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