Penfield Search Partners

Job DescriptionContact: Alexandra Spink - No 3rd party candidatesOur client is seeking a Medical Writing Editor to support quality control (QC) review copyediting and submission readiness for clinical and regulatory documents. This role partners with Medical Writers and cross-function

Job DescriptionContact: Alexandra Spink - No 3rd party candidatesOur client is seeking a Medical Writing Editor to support quality control (QC) review copyediting and submission readiness for clinical and regulatory documents. This role partners with Medical Writers and cross-function

Job DescriptionContact: Neisha Camacho/Terra Parsons -No 3rd party candidatesClinical Data Management LeadCNS Focus / Phase II DevelopmentWe are partnering with a growing biotech organization that is seeking a Clinical Data Management Lead to support ongoing and upcoming clinical prog

Job DescriptionContact: Neisha Camacho/Terra Parsons -No 3rd party candidatesClinical Data Management LeadCNS Focus / Phase II DevelopmentWe are partnering with a growing biotech organization that is seeking a Clinical Data Management Lead to support ongoing and upcoming clinical prog

Job DescriptionContact: Alexandra Spink -No 3rd party candidatesThis role is 100% on site in Miramar FL.Position DescriptionThe Study Physician is responsible for ensuring the medical safety eligibility and ongoing clinical oversight of study participants in accordance with the protoc

Job DescriptionContact: Alexandra Spink -No 3rd party candidatesThis role is 100% on site in Miramar FL.Position DescriptionThe Study Physician is responsible for ensuring the medical safety eligibility and ongoing clinical oversight of study participants in accordance with the protoc

Job Description Contact: Alexandra Spink - No 3rd party candidatesWe are seeking an experienced Regulatory Medical Writer to provide fractional support for the development of complex regulatory submission documents. Requires a writer who can lead doc

Job Description Contact: Alexandra Spink - No 3rd party candidatesWe are seeking an experienced Regulatory Medical Writer to provide fractional support for the development of complex regulatory submission documents. Requires a writer who can lead doc

Job DescriptionContact: Neisha Camacho/Terra Parsons -No 3rd party candidatesWe are seeking a highly experienced Statistical Programmer to lead programming activities across global clinical studies. This role operates beyond executional programming with responsibility for oversight of

Job DescriptionContact: Neisha Camacho/Terra Parsons -No 3rd party candidatesWe are seeking a highly experienced Statistical Programmer to lead programming activities across global clinical studies. This role operates beyond executional programming with responsibility for oversight of

Job DescriptionContact: Neisha Camacho/Terra Parsons -No 3rd party candidatesThe Principal of Pharmacoepidemiology will provide leadership for epidemiologic studies and analyses using various data sources administrative claims data/EMR. They are responsible for providing epidemiologic

Job DescriptionContact: Neisha Camacho/Terra Parsons -No 3rd party candidatesThe Principal of Pharmacoepidemiology will provide leadership for epidemiologic studies and analyses using various data sources administrative claims data/EMR. They are responsible for providing epidemiologic