Clinical Pharmacologist Jobs in Coryell County, Texas

The Senior Clinical Pharmacologist responsibilities include assisting the planning and execution of the Clinical Development ......  More »    Fewer «   Plan for NCE(s) particularly as it applies to the discipline of Clinical Pharmacology. Can conduct, mentor and QC non-compartmental pharmacokinetic analyses. Duties may include setting or influencing the scientific directions for cross-functional team members and other members of the department. The Senior Clinical Pharmacologist will optimize interdisciplinary understanding and synergy within the Group(s) and integrate activities with those of other Departments and Teams to help shape cohesive development plans. These duties may include leading teams and independently initiating and carrying out necessary tasks to accomplish Vertex goals. Key Responsibilities * Responsible for operational leadership within the clinical pharmacology department and within the companyâs matrix for drug development           Fewer «

The Clinical Pharmacology Associate will be responsible for providing hands-on support on day to day activities in the ......  More »    Fewer «   department. This individual will closely work with lead Clinical Pharmacologist to initiate the studies. This individual will participate in departmentâs business processes of data acquisition, quality control and overall process improvement. Key Responsibilities: * Provide support to lead Clinical Pharmacologist in study initiation * Perform preliminary analysis of pharmacokinetic data * Prepare data specification in SDTM CDISC format * Review data transfer by vendors * Perform Quality Control (QC) of Pharmacokinetics section of the Clinical Study Report (CSR) * Responsible for maintaining excellent working knowledge of pharmacokinetics data, design and phases of clinical studies and relevant regulatory requirements Minimum Requirements * Bachelorâs degree in quantitative discipline or biological sciences with significant courses in quantitative area.           Fewer «

Auto req ID 3572BR Job Title Study Manager, Clinical Pharmacology Functional Area Research & Development City Edison State ......  More »    Fewer «   New Jersey Job Description Job Summary: The incumbent will be responsible for the implementation and day-to-day coordination of TMCP studies conducted in North America or aligned territories. Drug candidates under investigation may belong to any therapeutic area, however the candidate will be responsible for delivering Oncology Phase 1 studies in a clinical setting. This individual will coordinate with the Clinical Pharmacologist and Translational Medicine Lead (as appropriate to the primary TMCP function responsible for the study) as well as other functional contacts to ensure TMCP studies are conducted according to the timelines and objectives set forth by the Operational Plan, and per Daiichi-Sankyo SOPs, SWPs and ICH GCP Guidelines.           Fewer «

The Clinical Pharmacology Associate will be responsible for providing hands-on support on day to day activities in the ......  More »    Fewer «   department. This individual will closely work with lead Clinical Pharmacologist to initiate the studies. This individual will participate in departmentas business processes of data acquisition, quality control and overall process improvement.AKey Responsibilities:AProvide support           Fewer «

Auto req ID 3572BRJob Title Study Manager, Clinical PharmacologyFunctional Area Research and DevelopmentCity EdisonState New ......  More »    Fewer «   JerseyJob DescriptionJob Summary:The incumbent will be responsible for the implementation and day:to:day coordination of TMCP studies conducted in North America or aligned territories. Drug candidates under investigation may belong to any therapeutic area, however the candidate will be responsible for delivering Oncology Phase 1 studies in a clinical setting. This individual will coordinate with the Clinical Pharmacologist and Translational Medicine Lead as appropriate to the primary TMCP function responsible for the study as well as other functional contacts to ensure TMCP studies are conducted according to the timelines and objectives set forth by the Operational Plan, and per Daiichi:Sankyo SOPs, SWPs and ICH GCP Guidelines.Responsibilities:Interface with Clinical Study Lead and Outsourcing to develop and manage project budgets for sites           Fewer «

In this role, the individual will be managing multiple Phase I studies along with managing a CRO. The Clinical ......  More »    Fewer «   Pharmacologist will be involved in analyzing complex Pharmacodynamic data, performing PKPD simulation/modeling, and analyzing Phase I Drug to Drug interactions. The Clinical Pharmacologist will be involved with the Schizophrenia therapeutic area for about 50% of the time, and will also be involved with other therapeutic indications.Our client would like at least five years of experience in the Pharmaceutical/Biopharmaceutical industries with an advanced degree; Masters, PharmD, PhD or M.D. The individual will not have direct reports at the beginning, but can look forward to a promotion within a year and will eventually be managing people.This is a "ground floor" opportunity for a "hands-on" expert who enjoys visibility and has the drive and personal skills to make a difference in the drug development process. CNS experience a plus.Northern, NJ           Fewer «

Job Title: Assoc Dir, Clin Pharmacology Profession: Biotechnology/Pharmaceuticals -> Clinical Development Professionals JOB ......  More »    Fewer «   TITLE------ Assoc Dir, Clin PharmacologyRequisition Number------ 6399BRDepartment Name------ Clinical PharmacologyLocation------ Cambridge, MAPOSITION SUMMARY------ The Clinical Pharmacologist has the overall responsibility and accountability of the clinical pharmacology components of drug development and represents clinical pharmacology on the Clinical Subteam/and Core team. He/she applies high medical, scientific, and ethical standards to define the clinical pharmacology characteristics (pharmacokinetics, and pharmacodynamic) of investigational drugs in a cost and time-efficient manner.DUTIES & RESPONSIBILITIES------ ------- Provide clinical pharmacology expertise in order to:o------ Develop the timely, scientifically sound           Fewer «

This role is responsible for the integration of people, process and technology for the clinical pharmacologist (analysts of ......  More »    Fewer «   clinical data). The integration programs utilize an established PM framework based upon PMI. All projects have a project owner, project steering board, and executive sponsor to provide governance. Each project Phases (Business Requirements, Design, Deployment, Testing, Handover, and Decommission) must be signed off on by the project steering board. Responsibilities: * Create and executes project work plans and revises as appropriate * Effectively applies company project methodology and enforces project standards * Create Project documentation as appropriate (utilizing templates as a base) * Project Management Plan * Business Requirements * Solution Design * Test plans and approach * Deployment document * Handover * Lessons Learned * Project RAID log * Project status report * Ensures project documents are complete, current, and stored appropriately           Fewer «

Title: Project Manager Location:Collegeville, PA Rate Range : Open Type: Contract, 6 months Description: The integration ......  More »    Fewer «   programs utilize an established PM framework based upon PMI. All projects have a project owner, project steering board and executive sponsor to provide governance. Each project Phases (Business Requirements, Design, Deployment, Testing, Handover, Decommission) must be signed off on by the project steering board. One component of these efforts is the integration of people, process and technology for the clinical pharmacologist (analysts of clinical data). Responsibilities: a) Create and executes project work plans and revises as appropriate b) Effectively applies companyandrsquo;s project methodology and enforces project standards.           Fewer «

Title: Project Manager Location: Collegeville, PA Rate Range : Open Type: Contract, 6 months Description: The integration ......  More »    Fewer «   programs utilize an established PM framework based upon PMI. All projects have a project owner, project steering board and executive sponsor to provide governance. Each project Phases (Business Requirements, Design, Deployment, Testing, Handover, Decommission) must be signed off on by the project steering board. One component of these efforts is the integration of people, process and technology for the clinical pharmacologist (analysts of clinical data). Responsibilities: a) Create and executes project work plans and revises as appropriate b) Effectively applies company's project methodology and enforces project standards. c) Create Project documentation as appropriate (utilizing templates as a base) ÷ Project Management Plan ÷ Business Requirements ÷ Solution Design ÷ Test plans and approach ÷ Deployment document ÷ Handover ÷ Lessons Learned ÷ P           Fewer «

PRIMARY FUNCTION / MAJOR RESPONSIBILITIES: Prepares scientific reports and presentations using available software and ......  More »    Fewer «   templates. Reviews clinical protocols. Brings together all necessary data and information to prepare scientific reports; keep multiple reports moving forward simultaneously (multi-tasking). Serves as a focal point of communications among report authors and between report authors and reviewers. Complies with procedures set forth in: Departmental Guidelines Relevant IQS documents Study protocols Other directives issued by the management regarding clinical/ preclinical studies. Ensures scientific integrity of all processes. Applies the most current electronic document conventions and processes consistently and accurately. Provides PK/PD information to internal peers and department management. Committed to producing work of the highest quality Pays close attention to detail SUPERVISORY RESPONSIBILITIES: May mentor departmental personnel. ACCOUNTABILITY / SCOPE:           Fewer «

Pharmacologist/Toxicologist - Radiological Therapeutics Full Time Regular posted 7/16/2010 Job Category SCT - ......  More »    Fewer «   Scientist Req ID 178825 Able to obtain security clearance? Secret Currently possess security clearance? None Location Washington, DC % Travel 25 Relocation No RecruiterID: 3571 Requirements The Life Sciences Operation of the Health Solution Business Unit is seeking a Pharmacologist/Toxicologist Subject Matter Expert (SME) to support the Chemical/Radiological/Nuclear (CRN) Medical Countermeasures group within the Biomedical Advanced Research and Development Authority (BARDA) of Health and Human Services. The CRN group at BARDA maintains a large portfolio of medical countermeasures (MCMs) and diagnostics with the objective to provide suitable products to the Strategic National Stockpile (SNS) through US Government acquisition mechanisms. This full time position will perform duties at the customer site in Washington, D.C.           Fewer «

ORIGINAL JOB LISTING Pharmacologist Location Rockville, MD Job ID 2998 Employment Status Full-Time Regular Required ......  More »    Fewer «   Experience 5-10 years Required Education Doctorate Degree or Equivalent Required Travel No Relocation Available Yes Summary/Description Human Genome Sciences (HGS) is a biopharmaceutical company with approximately 800 employees and world-class R&D and manufacturing facilities based in Rockville, MD. We have three promising products in late-stage development one, raxibacumab, already commercialized with sales to the U.S, Government and two products moving toward commercialization, BENLYSTA (formerly LymphoStat-B) and ZALBIN (formerly Albuferon). We are developing both of these products in collaboration with world leaders in the pharmaceutical industry.           Fewer «

Qualifications: BA / BS or MS in biology, pharmacology, or related field Several years of laboratory research experience ......  More »    Fewer «  , with industry and laboratory animal experience being highly desirable CANCER EXPERIENCE VERY HIGHLY DESIREABLE Description: The candidate will join the Pharmacology group to be part of a productive motivated team supporting the successful development of small molecule therapeutics for the treatment of cancer. This scientist will perform experiments in established disease models, as well as participate in the development of novel models relevant to improving the lives of cancer patients. Experience in small animal handling is required and with in vivo tumor modeling is preferred. Familiarity with aseptic techniques, such as tissue culture and small animal surgical experience are requested. Duties:           Fewer «

Job Family: Scientists Job Category: Full-Time Job Classification: Experienced/Established Division: Global ......  More »    Fewer «   Pharmaceutical R and D Shift: First Overview: At Abbott, we provide the perspectives and experience necessary to translate science into real solutions for patients in over 130 markets worldwide. Today, 72,000 Abbott employees are doing work that matters. Job Description: PRIMARY FUNCTION / MAJOR RESPONSIBILITIES: Prepares scientific reports and presentations using available software and templates. Reviews clinical protocols. Brings together all necessary data and information to prepare scientific reports; keep multiple reports moving forward simultaneously (multi-tasking). Serves as a focal point of communications among report authors and between report authors and reviewers. Complies with procedures set forth in: Departmental Guidelines Relevant IQS documents Study protocols Other directives issued by the management regarding clinical/ preclinical studies.           Fewer «

Design, develop, characterize, implement and validate relevant in vivo oncology-related models including subcutaneous and ......  More »    Fewer «   orthotopic models for profiling the pharmacological effects of drug candidates . Carry out ex vivo pharmaco-dynamic studies tailored to the molecular target of interest . Documentation, analysis and interpretation of experiments for the evaluation of pre-clinical candidates . Present results within a multidisciplinary team environment Minimum requirements B.A/B.S. or technical equivalent with expertise in in vivo physiology or pharmacology. Industry experience with oncology models is strongly preferred. Individuals with experience in molecular biology techniques are strongly encouraged to apply. Candidates will be expected to possess: . Hands on in vivo skills necessary to validate and implement rodent oncology models including dosing and tumor implantation techniques. Experience with models derived from primary patient samples a plus.           Fewer «

The successful candidate will join a dynamic, multi-disciplinary team of scientists in the In Vivo Pharmacology Oncology ......  More »    Fewer «   Group, playing a key role in the development of in vivo models of cancer and the use of those models for evaluating new drug candidates. Ideal applicants will possess excellent communication and organizational skills, critical problem-solving abilities, and a commitment to excellence. Candidate will be responsible for: • Design, develop, characterize, implement and validate relevant in vivo oncology-related models including subcutaneous and orthotopic models for profiling the pharmacological effects of drug candidates • Carry out ex vivo pharmaco-dynamic studies tailored to the molecular target of interest • Documentation, analysis and interpretation of experiments for the evaluation of pre-clinical candidates • Present results within a multidisciplinary team environment           Fewer «

Job Title RESEARCH PHARMACOLOGIST AutoReqId 76399BR Job Family Scientists Job Category Full-Time Job Classification ......  More »    Fewer «   Experienced/Established Division Global Pharmaceutical R and D Shift First Overview At Abbott, we provide the perspectives and experience necessary to translate science into real solutions for patients in over 130 markets worldwide. Today, 72,000 Abbott employees are doing work that matters. Job Description PRIMARY FUNCTION / MAJOR RESPONSIBILITIES: Prepares scientific reports and presentations using available software and templates. Reviews clinical protocols. Brings together all necessary data and information to prepare scientific reports; keep multiple reports moving forward simultaneously (multi-tasking). Serves as a focal point of communications among report authors and between report authors and reviewers. Complies with procedures set forth in: Departmental Guidelines Relevant IQS documents Study protocols           Fewer «

Job ID 70297BR Posting Title Oncology Pharmacologist BS/MS Scientist Division NIBR Business Unit NIBR Country USA Work ......  More »    Fewer «   Location United States - Massachusetts Company/Legal Entity USA Novartis Institutes for BioMedical Research, Inc., Cambridge, MA Posting Functional Area Research Job Type Full Time Employment Type Permanent Job Description The successful candidate will join a dynamic, multi-disciplinary team of scientists in the In Vivo Pharmacology Oncology Group, playing a key role in the development of in vivo models of cancer and the use of those models for evaluating new drug candidates. Ideal applicants will possess excellent communication and organizational skills, critical problem-solving abilities, and a commitment to excellence. Candidate will be responsible for: . Design, develop, characterize, implement and validate relevant in vivo oncology-related models including subcutaneous and orthotopic models for profiling the pharmacological effects of drug candidates           Fewer «

Job Family: Scientists Job Category: Full-Time Job Classification: Experienced/Established Division: Global ......  More »    Fewer «   Pharmaceutical R and D Shift: First Overview: At Abbott, we provide the perspectives and experience necessary to translate science into real solutions for patients in over 130 markets worldwide. Today, 72,000 Abbott employees are doing work that matters. Job Description: This position is for a senior scientist who will work within a multidisciplinary team to coordinate and implement external translational biomarker studies at Abbott. The successful candidate will serve as the operational program manager for the Discovery AT Translational Sciences organization, which is focused on quantifying target interaction and physiological responses to therapy, as well as translating these responses as biomarkers to reduce risk for preclinical and clinical programs.           Fewer «