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Our client, a top 15 Pharmaceutical company in the world, is currently seeking a Graphic Designer for a 3 to 4 month contract, located in Cambridge, MA. u00a0rnBy working for..
Summary Develop Deep Learning solutions for medical imaging problems. 6 month Co-op assignment, must be able to work 40 hours per week Must be a current fulltime student and returning..
Executive Director, Systems Immunology in Cambridge Massachusetts ROLE SUMMARY This role will lead a group of senior leaders in the computational biology, molecular profiling, cytometric profiling and external alliances disciplines..
n Under the direction of the Pharmacy Utilization Management (UM) Supervisor, the Clinical Pharmacist is responsible for reviewing, processing and managing the daily caseload of pharmacy prior authorization (PA) requests..
Boston, MA What you'll be doing Lead regulatory strategy for neurology products (IND/NDA/CTA/MAA) in various stages of pipeline. Direct external agencies and internal management to define regulatory pathways. Act as..
Under the direction of the Pharmacy Utilization Management (UM) Supervisor, the Clinical Pharmacist is responsible for reviewing, processing and managing the daily caseload of pharmacy prior authorization (PA) requests for..
Qualifications Bachelor's Degree and RN preferred in Nursing 4 years of progressively responsible work experience in patient care or clinical research, preferably in an academic medical center environment Experience with..
Work as a statistical programmer on drug development project teams. Responsibilities Support the inferential analysis of key safety and efficacy endpoints from clinical trials. Primary responsibilities include the production of..
Cambridge, MA What you'll be doing Provides scientific leadership in medicinal chemistry for cardio vascular metabolic and endocrine (CVMED) research unit (RU). Responsible for delivering project objectives with allocated resources..
Associate Director, Clinical Operations (GMA)','1700397','!*! Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future..
Qualifications Masters or Bachelor’s degree with 3 years programming experience in the pharmaceutical industry or equivalent experience Proficiency in SAS/BASE, STAT, GRAPHICS and MACRO.Proficiency in SAS/BASE, STAT, GRAPHICS and MACRO..
Qualifications 6 years’ experience in academic or pharmaceutical setting Ph.D. in statistics or MPH or equivalent degree Experience supporting Medical Affairs/publication of analysis results (e.g. abstracts, posters, manuscripts) a plus..
Manage a team of experienced data management staff (4-5) who support four Lysosomal Storage Disorder Registries. Responsibilities Provide functional line management for multiple projects and prioritize with respect to project..
Qualifications PharmD, M.D., DO, Ph.D., NP with 10 years of relevant clinical, scientific and/or industry medical affairs experience Experience in CNS/Psychiatry and/or Women’s health experience preferred..
The Aging group in Cambridge is looking for a highly motivated Associate-level scientist to join an interdisciplinary team dedicated to work in preclinical pharmacology models of human disease, with a..
The Associate Clinical Development Director (Assoc. CDD) is responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data. May be responsible for..