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Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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Academic/PhD degree in Biochemistry, Biology, Bioengineering, Immunology, or related discipline. Principal Scientist, Protein Production and Process Development. and with proteins expressed in mammalian cells with oversight of both upstream and downstream process development.
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Clinical or health sciences degree required with current or previous professional licensure strongly preferred (e.g., RN, RPh, PharmD, PA, DNP, MD, or PhD in a medically related field) from an accredited college or university.
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Keywords: ACCSLPHA, LCSW, LICSW, LMHC, LMFT, BCBA, LADC, Licensed Clinical Social Worker, Licensed Independent Clinical Social Worker, Licensed Mental Health Counselor, Licensed Marriage and Family Therapists, Community Based, Clinician, Outpatient, VinfenLPHA.
$70,300 - $74,000 a yearPart-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The ideal candidates will have scientific lab experience with hands-on experience in a lab environment (academic or professional) and are looking to expand their expertise in FLOW Cytometry, further developing their skillset in the development and validation of FLOW, Cell based and PD (biomarker) assays.
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About PepGen PepGen Inc. is a clinical-stage biotechnology company advancing the next-generation of oligonucleotide therapies with the goal of transforming the treatment of severe neuromuscular and neurological diseases.
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RIO supports clinical trials research informatics systems for the DF/HCC member institutions regarding oncology research. The Research Informatics Operations (RIO) Director, Account Services for Clinical Trials Research works closely with Dana-Farber clinical research stakeholders and functional leaders within I&A to identify, prioritize, and address the clinical research data informatics needs of DFCI.
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Under the supervision of the Program Director, and in collaboration with Principal Investigators, the Clinical Research Coordinator contributes to clinical research studies in the Ocular Melanoma Center.
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Translational Computational Biology: Bridge the gap between target discovery and clinical applications, translating molecular insights into innovative therapeutic strategies. You will be a key team member responsible for utilizing NextMAPTM, a NextRNA proprietary computation engine that identifies driving disease lncRNAs∯*∯ You will have an opportunity to work with a diverse team of bioinformaticians, biochemist, chemists, and biologist to support drug discovery programs for next wave of RNA therapeutics.
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Minimum of 5 years' experience with GCP/GCLP regulations and testing in support of clinical trials. Along with the CLIA Lab Director and leadership, maintain laboratory audit readiness by overseeing and managing clinical lab audits with regulators, pharmaceutical partners, and with other agencies, ensuring that internal system and process audits are scheduled and conducted.
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Academic and judicial sanctions approved by Academic Deans, Dean of Students. Serve as the contact person for WIT students participating in Study Abroad programs and communicate academic information as requested.
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Posted job title: RAD - INTRA CL Interventional Radiology CL. About Cross Country Allied Applicants must have at least 1-2 years of POST CLINICAL work experience Craving an adventure? Job Description & Requirements Specialty: Interventional Radiology Technologist Discipline: Allied Health Professional Start Date: 06/17/2024 Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel Job Description As a cardiac cath lab technologist in interventional radiology, you'll assist the physician with catheterization of the heart and other minimally invasive procedures.
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Reporting to the VP of Program Strategy & Management, this person will work collaboratively to manage and integrate diverse R&D activities including but not limited to, preclinical research, clinical development, CMC, regulatory affairs, new product planning, business development and finance.
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Experience with vivarium responsibilities including non-clinical ocular imaging, animal handling, intravitreal injection, eye dissection, perfusion is required. As a member of the Translational Development group, the applicant will play a crucial role in advancing our understanding of ocular diseases and developing therapeutic strategies for future clinical practice by targeting the complement cascade.
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Oversight of the creation of a compelling scientific communications and publication plan based on the clinical trials conducted within Pfizer Oncology. Pfizer’s in-line portfolio is focused on four broad, key areas: breast cancer, genitourinary cancer, hematology and precision medicine, complemented by an extensive pipeline of over 50 programs in clinical development.
$299,600 - $499,400 a yearFull-timeExpandApply NowActive JobUpdated Yesterday
academic clinical trials jobs Company: Emory University in Cambridge, MA
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