- Merck & Co. (North Wales, PA)
- …through interaction with key scientific leaders.Specifically, the Senior Principal Scientist is responsible for:Planning clinical trials (design, operational ... Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide...timely and equitable access to our medicines.The Senior Principal Scientist has primary responsibility for protocol development and medical/scientific… more
- Merck & Co. (North Wales, PA)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the strategic planning and directing clinical research activities ... compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical development,… more
- Pfizer (Collegeville, PA)
- …the development team to establish, lead, coordinate, and execute the early oncology clinical development plan(s). You will lead the development of the clinical ... protocol and participate as an individual contributor on clinical teams with Pfizer development operations and the project team, to meet enrollment and study… more
- Merck & Co. (Upper Gwynedd, PA)
- …science of preclinical discovery into compounds ready for assessment in large clinical populations.We are seeking a highly qualified physician- scientist with a ... Job Description Senior Principal Scientist Translational Medicine, Immunology Translational Medicine in our...experience in the pharmaceutical industry and Immunology R&D and clinical and academic expertise in Immunology-related areas such as… more
- Merck & Co. (North Wales, PA)
- …or related field plus 5 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life Sciences, ... or related field plus 3 years SAS programming experience in a clinical trial environment Department Required Skills and Experience: Excellent communication (oral,… more
- Merck & Co. (North Wales, PA)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Merck & Co. (North Wales, PA)
- …drug/vaccine projects in Late Development Statistics.Lead the interaction with Clinical , Regulatory, Statistical Programming, Data Management, and other Scientists ... from our Research & Development Division in designing and analyzing clinical trials, and in coordinating the statistical activities for clinical drug/vaccine… more
- Merck & Co. (North Wales, PA)
- …This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.-The… more
- Merck & Co. (North Wales, PA)
- …for world-wide regulatory application submissions of drug and vaccine clinical development projects.Be accountable for submission data standards planning activities, ... keeping current with industry submission data standards including SDTM, ADaM, clinical site data for CDER inspection planning, etc.Responsible for continuous… more
- Eisai, Inc (Exton, PA)
- …proteins.Demonstrated knowledge of biopharmaceutical development through all clinical phases and post-commercialization.Strong familiarity with cGMP/ICH/FDA/EMA ... a must.Eisai Salary Transparency Language:The base salary range for the Scientist II, Analytical Outsource & Stability is from :113,400-148,900Under current… more
- Merck & Co. (North Wales, PA)
- Job DescriptionPrincipal Scientist (Director) - Outcomes Research - Gastric CancersThis position resides within our company's Value and Implementation (V&I), ... access in collaboration with internal teams, and provide input into clinical , payer/access, marketing and value evidence generation strategies and programs.In… more
- Kelly Services (West Point, PA)
- **Senior Clinical Scientist I** **Therapeutic Areas: Oncology & Immunology** **Description of Services** + May lead or support a study or studies, depending on ... size/complexity. If lead, accountable for the clinical /scientific execution of the protocol. + As lead, will...As lead, will be responsible for the following: + Clinical point of contact for scientific issues/questions for internal… more
- Kelly Services (West Point, PA)
- ** Clinical Scientist ** **Therapeutic Areas: Oncology and Immunology** **Description of Services** + Assists the CS Protocol Lead and study team with the ... clinical /scientific conduct of clinical studies eg, adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials,… more
- Lilly (Philadelphia, PA)
- …better for people around the world. **Organization Overview:** The Senior Director - Clinical Imaging Research Scientist role will occupy a key position within ... image analysis group to support quantitative analysis of images obtained within clinical trials across therapeutic areas such as Oncology, Diabetes, Immunology, and… more
- Merck (North Wales, PA)
- …through interaction with key scientific leaders. **Specifically, the Senior Principal Scientist is responsible for:** + Planning clinical trials (design, ... **Job Description** Our Clinical and Pharmacovigilance teams manage studies to provide...and equitable access to our medicines. The Senior Principal Scientist has primary responsibility for protocol development and medical/scientific… more
- Pfizer (Collegeville, PA)
- …You will be responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the ... Late-Stage Oncology portfolio. **KEY RESPONSIBILITIES** + Clinical development expert for assigned studies maintaining current scientific and clinical knowledge… more
- Pfizer (Collegeville, PA)
- …the development team to establish, lead, coordinate, and execute the early oncology clinical development plan(s). You will lead the development of the clinical ... protocol and participate as an individual contributor on clinical teams with Pfizer development operations and the project team, to meet enrollment and study… more
- Merck (North Wales, PA)
- **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the strategic planning and directing clinical research ... compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical development,… more
- Merck (North Wales, PA)
- **Job Description** Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and… more
