- Pfizer (Groton, CT)
- …the way in healthcare and make a lasting impact on society. **What You Will Achieve** As a Clinical Study Group Lead , you will be an operational and ... 5 submission subteams and endgame inspection readiness. In the Clinical Study Group Lead... studies + Accountable to deliver excellence in clinical study team leadership for a portfolio… more
- Takeda Pharmaceuticals (Providence, RI)
- …mission. **_GOALS:_** + Develop strategy for technology selection and deployment across Clinical Studies in alignment with established Takeda SOPs & Policies, ... are met with the highest degree of quality. + Lead study level technology & vendor oversight...in preparing function for submission readiness and may represent Clinical Trial Tools & Technologies (CT3) group … more
- Pfizer (Groton, CT)
- …Intake processes to optimize efficiency and compliance with regulatory requirements. + Lead and manageaudits within the Study Organization (SO), including ... (R&D) engine providing analytics & intelligence to customers and stakeholders across clinical and regulatory functions within PRD & POD. The Site Intelligence,… more
- Takeda Pharmaceuticals (Providence, RI)
- …data cleaning and reconciliation efforts and work cross-functionally with all members of Clinical Study teams to foster an environment of quality and efficient ... integrating, execution, build and oversight of clinical trial deliverables. The Clinical Data Sciences group is responsible for integrating structured and… more
- Norstella (Providence, RI)
- …all the content applications across Norstella. As part of a large technology group , the Technical Lead will work with product management, architecture and ... Technical Lead - Content Engineering Company: Norstella Location: Remote,...access. Each organization (Citeline, Evaluate, MMIT, Panalgo, The Dedham Group ) delivers must-have answers for critical strategic and commercial… more
- Edwards Lifesciences (Providence, RI)
- …As **Senior Manager, Biostatistics, TMTT** , you will use your expertise as biostatistical lead in clinical study design projects for pivotal trials, while ... activities to ensure proper design, analysis, and presentation of clinical studies . **How you will make an...will make an impact:** + Act as core team member/ lead biostatistician of assigned clinical trial(s) in… more
- IQVIA (Johnston, RI)
- …analysis, interpretation, and dissemination of findings. In particular, the QualityMetric group within IQVIA focuses on clinical outcome assessment (COA) ... quantitative research services team supports a broad range of studies aimed to better understand the patient's experience related...role should be a scientist first, who can also lead and develop talent and will be responsible for… more
- Sumitomo Pharma (Providence, RI)
- …Medical Science Liaisons (MSLs) within the specified region to achieve clinical , strategic and business objectives. This position works cross-functionally to ... as supporting evidence generation efforts through company- and investigator-led studies , as appropriate. This role will also be responsible...of the Field MSL organization's goals and objectives. + Lead , manage and mentor, the Field MSLs to ensure… more
- Hartford HealthCare (Norwich, CT)
- …collaboration with attending surgeon, this role is responsible for establishing a new clinical program while providing skilled health care to patients in a variety ... of clinical settings and facilitating clinical management of...outreach | Ensures timely retrieval of laboratory and ancillary studies and diagnostic consultation reports | Consults with appropriate… more
- Merck (Providence, RI)
- …training, and prioritization of Global Plans for USMA. + As a core member (or co- lead ) of the US Regional Medical Affairs Team (RMAT), the SDMA partners with the ... US Regional Director of Medical Affairs (RDMA) (where applicable), US Global Clinical Trial Organization, Global Medical and Scientific Affairs (GMSA) TA leads, and… more
- Pfizer (Groton, CT)
- …of Pfizer's newest drug candidates and evaluate their suitability for progression into clinical studies and ultimately to commercialization. You will have a ... discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and...commercial launch. As a Director in the Materials Science group , you will lead a team of… more
- Sumitomo Pharma (Providence, RI)
- …team and play a highly visible role internally and externally, and effectively lead and communicate with cross-functional team members to develop and execute the ... costs to keep within budget of Medical Affairs. + Lead , develop and mentor team members. + Specify, develop...the medical/scientific community to develop close relationships with a group of scientific key opinion leaders. + Work closely… more
- Sumitomo Pharma (Providence, RI)
- …internal company programs and external facing interactions. This job will effectively lead and communicate with cross-functional team members to share and gain ... and healthcare payers. + Serve as a Medical Strategy lead for the Pfizer alliance for Women's Health, ensuring...the medical/scientific community to develop close relationships with a group of scientific key opinion leaders. + Work closely… more
- Pfizer (Groton, CT)
- …in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities ... will be performing laboratory and pilot-scale process characterization and process optimization studies . You will help Pfizer develop new and improved processes used… more
- Pfizer (Groton, CT)
- …Achieve It** + Apply technical skills to projects/ assignments within own work group /project team + With guidance, conduct scientific studies to support design ... discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and...and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's… more