- Merck & Co. (Rahway, NJ)
- …Laboratory Practice (GLP) studies . The Associate Principal Scientist is the primary clinical study team leader and has overall responsibility for a study ... Respect - Inclusion.Design and organization of paper and Electronic Data Capture (EDC) clinical studies that meet scientific and regulatory requirements by the… more
- Merck & Co. (Rahway, NJ)
- …assessments of external opportunitiesThe Senior Director May: Supervise the execution of clinical studies . Work closely with a cross-functional group ... manage the entire cycle of late-stage clinical development and studies , including development strategy, study design, initiation, execution, monitoring,… more
- Insmed Incorporated (NJ)
- …You'll Do: Participate in cross functional teams to develop and implement Clinical Study protocols within clinical program(s). Responsibilities include ... the future of science, we're in. Are you?About the Role:The Associate Director, Clinical Research Scientist will support and work predominately with the Medical… more
- Merck & Co. (Rahway, NJ)
- …of Phase I studies ; close collaboration with internal and external clinical study support staff and scientists (including discovery research, biostatistics, ... insight into the earliest stages of target identification and validation, and executing clinical studies to evaluate the relevance of potential targets to human… more
- Merck & Co. (WY)
- …ExperienceDemonstrated record of scientific/medical publication#eligibleforERPRequired Skills: Accountability, Clinical Affairs, Clinical Studies , ... questions from SLs, including questions about Company products. The work of an RMSD is aligned to: Scientific Exchange,...barriers to patient enrollment and retention efforts to achieve study milestonesUpon request from Global Clinical Trial… more
- Merck & Co. (Rahway, NJ)
- …holders and others. To prepare outcomes research protocols, statistical analysis plans, clinical study reports and manuscripts intended for peer-review. To ... objectives To inform and contribute to the value evidence strategy and associated studies which describe clinical , economic, and patient-centered unmet needs and… more
- Merck & Co. (Rahway, NJ)
- …- DayValid Driving License:NoHazardous Material(s):n/aRequired Skills:Biostatistics, Clinical Development, Clinical Immunology, Clinical Study Design, ... the project as needed.-This includes the following activities:1. Is involved in late clinical development planning (LDP) to ensure that study designs are… more
- BioAgilytix (Durham, NC)
- …their expertise in regulated bioanalysis and contribute directly to preclinical, clinical , and product release studies .At our organization, we're dedicated ... chromatographic and mass spectrometric (LC/MS) techniques in support of preclinical, clinical , and product release studies .Design, plan, and execute experiments… more
- Insmed Incorporated (NJ)
- …the Role:The Manager, Programming will provide statistical programming and analytic support clinical studies . As a team member of the Programming function, ... analytic reports, tables, figures, and slides in support of clinical study and other reports.Professional development to...Statistics, Computer Science, Mathematics, Engineering or related field of study is a plus.Minimum 5-7 years of work… more
- Insmed Incorporated (NJ)
- …HEOR research including burden of illness studies , patient reported outcomes studies and clinical trial endpoint selection, disease natural history, medical ... four consecutive years, certification as a Great Place to Work ® in the US, and a place on The...the company including market access, marketing, medical affairs, and clinical development to understand and support Insmed's business needs.… more
- Merck & Co. (Rahway, NJ)
- …product and manufacturing process characterization, drug product stability studies , specification development, manufacturing process scale-up and validation support, ... communication skills, demonstrated creativity, and strong interpersonal skills Ability to work in a team environment with cross-functional interactions - Preferred… more
- Merck & Co. (Rahway, NJ)
- …and outside of Device Development & Technology. The incumbent must be able to work well with employees at all levels to effectively engage and coordinate the ... and execute design verification strategies that successfully supports the clinical instruction(s) and commercial market approval(s) of combination products.Principal… more
- BioAgilytix (San Diego, CA)
- …them.The Manager II will lead scientific and operational activities in support of preclinical, clinical , and product release studies for our San Diego lab. This ... team(s) developing and validating bioanalytical assays for support of preclinical, clinical and product release studies .Motivating team by inspiring employees… more
- Insmed Incorporated (NJ)
- …gaps and provide support to the processes related to Investigator Initiated Studies . Work collaboratively with key intra- and inter- departmental partners (Field ... four consecutive years, certification as a Great Place to Work ® in the US, and a place on The...the design and execution of Phase 4 company sponsored studies , including HEOR studies and registries.Lead and… more
- Insmed Incorporated (San Diego, CA)
- …magazine's No. 1 Top Employer for four consecutive years, certification as a Great Place to Work ® in the US, and a place on The Sunday Times Best Places to Work ... will lead and oversee EDC programming, and database build for in-house clinical trials. This role will be responsible for the development and implementation… more
- Merck & Co. (North Wales, PA)
- … clinical bioanalysis.Required Skills: Anatomic Pathology, Biomarker Development, Clinical Studies , Digital Pathology, Molecular PathologyPreferred Skills: ... Molecular Biomarkers is responsible for translating preclinical molecular biomarkers to clinical development across all therapeutic areas and all phases of … more
- Merck & Co. (North Wales, PA)
- …Serves as the medical representative within Product Development sub-teams (including Clinical , V&I, Commercial, Publications, and Label), leveraging the GMSA vision ... meetings. Supports key countries with the development of local data generation study concepts and protocols when requested. Reviews Investigator-Initiated Study … more
- Merck & Co. (Rahway, NJ)
- …PK, PD and covariate dataProduce tables and graphics for inclusion in study reports and regulatory submissionsEnsure programmatic traceability from data source to ... or related field plus 5-9 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life Sciences,… more
- BioAgilytix (Durham, NC)
- …chromatographic and mass spectrometric (LC/MS) techniques in support of preclinical, clinical , and product release studies .Design, plan, and execute experiments ... we are growing. Our culture is fast-paced, fun and never boring. Because we work across numerous clients and drug modalities, your career can develop rapidly. You'll… more
- Merck & Co. (San Diego, CA)
- …and influence the design and execution of translational data generation from internal clinical studies . The individual will also play an important role in ... in the preparation of INDs and other submissions to health agencies for human clinical studies . As an Equal Employment Opportunity Employer, we provide equal… more
