- Merck & Co. (North Wales, PA)
- …or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life ... related field plus 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and Experience: Excellent interpersonal… more
- Merck & Co. (Upper Gwynedd, PA)
- … Clinical Judgment, Clinical Medicine, Clinical Reporting, Clinical Research Management, Clinical Trial Development, Communication, Data Analysis, ... serious diseases. --The Senior Director will report to an Associate Vice President in the Oncology Clinical ...an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of a supervisor,… more
- IQVIA (Wayne, PA)
- ** Associate Director, Clinical Trial Payments (CTP) Forecasting Services** Location: Remote, candidates must be US-based. Works in close collaboration with ... in order to provide high quality outcome for the clinical trial studies that have asked for...(Operations) + Management of the Forecasting Team, via the manager/ associate manager structure, that comprise mostly offshore team members.… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …more about Life at Olympus: https://www.olympusamerica.com/careers . **Job Description** The Sr. Clinical Trial Coordinator (Sr. CTC) will be responsible for ... and primary point of accountability and reconciliation for the Trial Master File (TMF) and the Investigator Site File...resolution of data queries under the guidance of the Clinical Research Associate (CRA), Data Management and/or… more
- Sumitomo Pharma (Harrisburg, PA)
- …Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable ... SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring that… more
- IQVIA (Philadelphia, PA)
- **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director/ Trial Delivery Manager (TDM) to lead and coordinate ... global and regional clinical trial management activities. This role ensures the successful planning, execution, and closure of clinical trials, whether… more
- Parexel (Harrisburg, PA)
- …associated with the set-up, running and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring Responsibilities and Study ... **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is...quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites… more
- ThermoFisher Scientific (Pittsburgh, PA)
- … clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant...(comparable to **10 Months - 2 years as traveling clinical research associate ** ). Valid driver's license… more
- Parexel (Harrisburg, PA)
- …activities associated with the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:** + Ensure proper ... The Senior Clinical Research Associate (Sr. CRA) is...quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites… more
- ICON Clinical Research (Blue Bell, PA)
- …a Senior Clinical Research Associate . + In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. + Strong organizational and ... Clinical Research Associate - Remote -... Clinical Research Associate - Remote - US ICON plc is...protocol compliance, data integrity, and patient safety throughout the trial process. + Collaborating with investigators and site staff… more
