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Job ID	Employer	Position	Description	Requirements	Location	Contact	Post Date
Details>>	Relypsa	Analytical Development Scientist to Associate Director Level (SN007)	DEPARTMENT:Pharmaceutical Development Relypsa has several positions open for Scientist to Associate Director level in the Analytical Development Group supporting late stage drug development project. Open positions may be filled with regular employees or temporary depending on applicable experience. RESPONSIBILITIES: •Strategic planning for Phase 3, NDA readiness •Method development for release/stability testing, reference standard characterization and impurities identification •Evaluation and improvement of existing tests and assays •Managing Phase 3 method validation and transfer at CRO and CMO •Reference standard programs and coordination of stability testing •Authoring and reviewing method development reports, validation and transfer protocols as well as related documents •Specification justifications for starting materials, intermediate, API, and drug product	SKILLS/EXPERIENCE: •Excellent working knowledge of the ICH Guidelines regarding GMP quality and stability testing, method validation and related GMP requirements for Phase 3 and beyond is a must •Recent direct experience with writing CMC analytical sections for NDA submission is required •Hands-on experience in wide range of state-of-the-art analytical techniques is a must (LC, LC/MS, IC, GC, GC/MS, SEC, IR, NMR, XRD, DSC, TA, Light Scattering) is desired •Direct involvement in overseeing and ability to build a highly productive relationship with CMO and CRO •Ability to exercise independent judgment in developing methods and evaluation criteria for obtaining results •Excellent communication, interpersonal and organizational skills for a team-oriented environment, along with the ability to be flexible and collaborate on projects QUALIFICATIONS: •BS, MS or PhD degree in Analytical Chemistry or related disciplines with recent experience in analytical function supporting late stage drug development	Santa Clara	apply-sn007@relypsa.com	2/5/2012 10:05:32 PM
Details>>	Relypsa	Scientist to Associate Director (SN008)	RESPONSIBILITIES: •Development of highly sensitive methods for impurities identification and quantification as well as reference standard characterization (literature search, devising strategies and exploring state-of-the art analytical techniques) •Evaluation and improvement of existing tests and assays •Authoring and reviewing method development reports and related documents •Managing analytical lab and coordinating analytical services	SKILLS/EXPERIENCE: •Hands-on experience in wide range of state-of-the-art analytical techniques is a must (LC, LC/MS, IC, GC, GC/MS, SEC, IR, NMR, XRD, DSC, TA, Light Scattering) is a must •Hand-on experience with running Waters, Dionex, and Agilent LC and GC instruments and familiarity with Empower, Masslynx, Chromeleon and Chemstation is required •Excellent working knowledge of the ICH Guidelines regarding GMP quality and stability testing, method validation and related GMP requirements for Phase 3 and beyond is preferred •Recent direct experience with writing CMC analytical sections for NDA submission is a plus •Direct involvement in overseeing and ability to build a highly productive relationship with CMO and CRO is a plus •Ability to exercise independent judgment in developing methods and evaluation criteria for obtaining results is desired •Works on complex problems where analysis of situations or data requires an evaluation of intangible variables •Excellent communication, interpersonal and organizational skills for a team-oriented environment, along with the ability to be flexible and collaborate on projects is required QUALIFICATIONS: PhD degree in Analytical Chemistry or BA/BS or MA/MS with appropriate work experience (generally at least 8+ years of work experience in a research and/or development environment; may have 2+ years of management experience). Postdocs with excellent academic track record will also be considered for jr level positions. •Sustained demonstration of leadership qualities in technical proficiency, scientific creativity, collaborations with others and independent thought •Is able to affect results by maneuvering through appropriate formal and informal organization channels – can reach appropriate resolution in many varied situations •Possesses exceptional ability to analyze and present applicable data •Possesses a reputation as an emerging leader in specific field with sustained performance and accomplishment •Has a track record of significant research publications in major peer-reviewed scientific journals •Demonstrates commitment and enhanced efficiency in quantity and quality of work •Additional competencies are demonstrated and evaluated, such as: management effectiveness, decision making and adaptability	Santa Clara	apply-sn008@relypsa.com	2/5/2012 10:05:26 PM
Details>>	Marrone Bio Innovations	Assistant Research Scientist – Discovery Chemistry	Marrone Bio Innovations is a leading global provider of natural products serving the ever expanding agricultural and water treatment markets. Venture backed and headquartered in Davis, California, the company focuses on discovering, developing, and marketing biopesticides for unmet pest and weed management needs. The following is a list of essential duties and responsibilities for this position. This list is not all-inclusive. This job description may be modified as needed. MAJOR RESPONSIBILITIES AND DUTIES: • Perform a variety of organic-analytical chemistry wet lab analyses, including extraction, solvent partition, and chromatography of compounds from microbial cultures. • Able to accurately use standard laboratory equipment (e.g., balances, pipettes, centrifuges, etc.) • Assists in performing analytical HPLC or GC method development and validation studies of analytes in a variety of matrices. • Assists in the isolation of bioactive compounds from complex microbial extracts utilizing flash or column chromatography, preparative HPLC, LCMS. • Ability to design and independently perform tasks and provide accurate results. • Effectively plans work schedule and able to utilize resources for timely completion of assigned projects. • Experience using computer programs Word, Excel, and PowerPoint. • Document and maintain legible, accurate, and complete laboratory records. • Good verbal and written communication skills. • Trains, mentors, and assists less experienced staff. • Maintains a clean and safe laboratory work environment. • Assists in writing reports and protocols, including SOPs and methods. • Promotes a cohesive team environment	MINIMUM QUALIFICATIONS AND CHARACTERISTICS: A successful candidate has a B.S. or M.S. in Chemistry, Biochemistry, or Analytical Chemistry with preferably 0-3 years of work experience. Experience with any of the following techniques would be a plus: centrifugation, UV, NMR, LCMS, flash and/or column chromatography, analytical and/or preparative HPLC, and lyophilization. The candidate is expected to have good organizational and record keeping skills and the ability to work effectively in a multi-project team environment and to collaborate with colleagues to achieve goals. Specific experience in bench scale laboratory processes relevant to preparation of agricultural or pharmaceutical chemical products is a plus.	Davis, CA	winman@marronebio.com	2/2/2012 1:38:49 PM
Details>>	Eli Lilly	Research Scientist - Toxicology (Job ID: 50418816)	Job Description For more than 130 years, Lilly has been dedicated to meeting the health care needs of people in the United States and around the world. We address these needs primarily by developing innovative medicines—investing a higher percentage of our sales in research and development than any other major pharmaceutical company. If you are interested in being considered for employment with a “Best in Class” Pharmaceutical company, please review the following opportunity: Research Scientist - Toxicology Eli Lilly & Co. is seeking a Research Scientist in Toxicology who will be working within Investigative Toxicology and as a partner with Pathology to address safety-related issues for molecules in all phases of development. The successful candidate will implement traditional and novel approaches in risk mitigation for the early portfolio enablement; and define and execute action plans directed to regulatory issue resolution for the later stage portfolio. KEY OBJECTIVES/DELIVERABLES: * Efficiently utilize in vitro and in vivo model systems and investigational tools including biomarker assays, imaging, transcript profiling, pharmacogenomics, and other novel approaches in translating preclinical risk to clinical risk assessment plans * Utilize knowledge of mammalian physiology in integrated investigative paradigms to compare and contrast pharmacodynamic and toxicity biomarkers * Actively engage in both in vivo and in vitro model development for direct application to portfolio issues * Lead laboratory scientists in novel assay investigation and qualification both internally and through the external resourcing strategy. Lilly credits its exceptional employees for its successes, and knows the key to ongoing achievement lies in attracting and retaining the best people. A company rich in heritage, Lilly employs individuals, conducts research and markets products worldwide. By providing for the unmet needs of our customers through a continuous stream of innovation, we will outgrow all competitors. Lilly earns consistent and wide recognition for creating an exceptional work environment while maintaining our highly regarded reputation in the Pharmaceutical Industry and Community. The following is a selection of awards and recognition Lilly has received in recent years: Awards and Recognition ELI LILLY AND COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER	MINIMUM REQUIREMENTS: * A Ph.D. in Toxicology, Cellular and/or Molecular Biology, or related field. * 3 to 7 years experience in pharmaceutical Toxicology or Pathology * Experience in utilization of models of cellular or tissue injury in assessing margins of safety and mechanisms of toxicity * Experience in the application of functional/physiological surrogate end-points to safety assessment * Published in reviewed scientific journals * Membership and engagement in toxicology and/or medical scientific organizations . ADDITIONAL PREFERENCES: * DVM or equivalent training in veterinary medicine * Experience in genomics, genetics, or system-level toxicology * Experience in regulatory aspects of Toxicology and Pathology * Demonstrated ability to effectively communicate in both oral and written forums * Demonstrated track record for working with multidisciplinary teams .	Indianapolis, Indiana	victoria.romera@lillyrecruiting.com	1/27/2012 6:20:01 AM
Details>>	Eli Lilly	Principal Research Scientist - Pathology (Job ID: 50428974)	Job Description For more than 130 years, Lilly has been dedicated to meeting the health care needs of people in the United States and around the world. We address these needs primarily by developing innovative medicines—investing a higher percentage of our sales in research and development than any other major pharmaceutical company. If you are interested in being considered for employment with a “Best in Class” Pharmaceutical company, please review the following opportunity: Principal Research Scientist- Veterinary Pathology Eli Lilly & Company is seeking an experienced veterinary pathologist.The individual selected for this position will be operating at a global level within Lilly and with its external partners to provide scientific leadership in interpreting toxicity and pharmacologic effects on physiology. This person will have access to many technical specialty groups within Lilly and its external partnerships, and will be expected to design, conduct and interpret the clinical and/or morphologic pathology portions of studies, and to identify and bring resolution to pathology and toxicology issues affecting the development of pharmaceuticals. An experienced veterinary pathologist with strong communication and negotiation skills will be required to partner with a world-class organization of scientists in Investigative Toxicology, Molecular Pathology, and the Therapeutic Area Business Units. KEY OBJECTIVES/DELIVERABLES: * Guidance in interpretation of pathology and toxicology data through active peer review and primary study assessment; * Developing clear and concise pathology contributor reports; * Provide scientific and regulatory perspectives on emerging issues and issue resolution plans; * Co-develop & orchestrate target and molecule-based risk mitigation strategies with Project Teams; * Represent Lillys assets in partnership with Toxicology project leaders across multiple therapeutic areas Lilly credits its exceptional employees for its successes, and knows the key to ongoing achievement lies in attracting and retaining the best people. A company rich in heritage, Lilly employs individuals, conducts research and markets products worldwide. By providing for the unmet needs of our customers through a continuous stream of innovation, we will outgrow all competitors. Lilly earns consistent and wide recognition for creating an exceptional work environment while maintaining our highly regarded reputation in the Pharmaceutical Industry and Community. The following is a selection of awards and recognition Lilly has received in recent years: Awards and Recognition ELI LILLY AND COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER	MINIMUM REQUIREMENTS: * DVM., Ph.D. and certification by American College of Veterinary Pathologists Academic or pharmaceutical experience in the regulatory aspects of GLP studies Experience in designing and interpreting Preclinical Safety & Investigative Studies ADDITIONAL SKILLS/PREFERENCES: * PhD preferred * ACVP certification	Indianapolis, Indiana	victoria.romera@lillyrecruiting.com	1/27/2012 6:18:17 AM
Details>>	Eli Lilly	Toxicology Project Leader (Job ID: 50429233)	Job Description: For more than 130 years, Lilly has been dedicated to meeting the health care needs of people in the United States and around the world. We address these needs primarily by developing innovative medicines—investing a higher percentage of our sales in research and development than any other major pharmaceutical company. If you are interested in being considered for employment with a “Best in Class” Pharmaceutical company, please review the following opportunity: Toxicology Project Leader The Toxicology Division is seeking a Senior Research Scientist who will represent the component on development teams as a Toxicology Project Leader as well as providing subject matter expertise in a scientific or regulatory area. The Toxicology Project Leader provides an integral role in developing world-class medicines for Eli Lilly and Company. KEY OBJECTIVES/DELIVERABLES: * A Toxicology Project Leader designs and implements aggressive, innovative nonclinical safety assessment plans for drugs in the pipe-line from the discovery phase through the launch of new medicines. * They are a critical member of teams developing novel new medicines, write the toxicology sections of regulatory documents and represent toxicology data to world-wide regulatory authorities. * Subject Matter Experts have responsibility for providing scientific positions on their area of expertise both inside and outside of the Toxicology component. * This includes assisting in study designs, data interpretation, and providing a position on the regulatory impact. * Use the best science to design and implement safety assessment plans for new medicines that meet world-wide regulatory expectations. * As a member of development teams, work effectively as a partner to meet corporate goals. * As a subject matter expert, work with Toxicology colleagues, development teams, and external experts to develop a strategy for identifying and solving issues in your area of expertise. * Work with development teams to fully integrate toxicology data into a risk assessment for patient safety. Lilly credits its exceptional employees for its successes, and knows the key to ongoing achievement lies in attracting and retaining the best people. A company rich in heritage, Lilly employs individuals, conducts research and markets products worldwide. By providing for the unmet needs of our customers through a continuous stream of innovation, we will outgrow all competitors. Lilly earns consistent and wide recognition for creating an exceptional work environment while maintaining our highly regarded reputation in the Pharmaceutical Industry and Community. The following is a selection of awards and recognition Lilly has received in recent years: Awards and Recognition ELI LILLY AND COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER Office located in Indianapolis.	MINIMUM REQUIREMENTS: * Ph.D. degree in Toxicology, or a Ph.D., D.V.M., or M.S. degree in a related science with extensive training in the field of Toxicology * At least 3 years of on-the-job experience in safety assessment as it relates to the pharmaceutical industry * Excellent verbal and written communication skills * Demonstrates thoughtful leadership skills ADDITIONAL SKILLS/PREFERENCES: * Strong interpersonal and team-building skills, including demonstrated experience working in a team environment * DABT or other relevant certification * Study Director for GLP studies * Experience working on development teams consisting of ADME, biology, chemistry, regulatory, and medical * Subject Matter Expertise in Endocrine biology, Neurobehavior, or Biotherapeutics including a network of contacts in the scientific community * Regulatory experience, including Pharm/Toxicology experience at a regulatory authority OTHER CONSIDERATIONS: * Candidates with more years of experience are encouraged to apply, since final consideration for employment, compensation, and job responsibilities will reflect the experience level. * Some travel.	Indianapolis, Indiana	victoria.romera@lillyrecruiting.com	1/27/2012 6:16:26 AM
Details>>	Eli Lilly	Toxicology Project Leader (Job ID: 50429316)	Job Description For more than 130 years, Lilly has been dedicated to meeting the health care needs of people in the United States and around the world. We address these needs primarily by developing innovative medicines—investing a higher percentage of our sales in research and development than any other major pharmaceutical company. If you are interested in being considered for employment with a “Best in Class” Pharmaceutical company, please review the following opportunity: Toxicology Project Leader The Toxicology Division is seeking a Senior Research Scientist who will represent the component on development teams as a Toxicology Project Leader as well as providing subject matter expertise in a scientific or regulatory area. The Toxicology Project Leader provides an integral role in developing world-class medicines for Eli Lilly and Company. KEY OBJECTIVES/DELIVERABLES: * A Toxicology Project Leader designs and implements aggressive, innovative nonclinical safety assessment plans for drugs in the pipe-line from the discovery phase through the launch of new medicines. * They are a critical member of teams developing novel new medicines, write the toxicology sections of regulatory documents and represent toxicology data to world-wide regulatory authorities. * Subject Matter Experts have responsibility for providing scientific positions on their area of expertise both inside and outside of the Toxicology component. * This includes assisting in study designs, data interpretation, and providing a position on the regulatory impact. * Use the best science to design and implement safety assessment plans for new medicines that meet world-wide regulatory expectations. * As a member of development teams, work effectively as a partner to meet corporate goals. * As a subject matter expert, work with Toxicology colleagues, development teams, and external experts to develop a strategy for identifying and solving issues in your area of expertise. * Work with development teams to fully integrate toxicology data into a risk assessment for patient safety. Lilly credits its exceptional employees for its successes, and knows the key to ongoing achievement lies in attracting and retaining the best people. A company rich in heritage, Lilly employs individuals, conducts research and markets products worldwide. By providing for the unmet needs of our customers through a continuous stream of innovation, we will outgrow all competitors. Lilly earns consistent and wide recognition for creating an exceptional work environment while maintaining our highly regarded reputation in the Pharmaceutical Industry and Community. The following is a selection of awards and recognition Lilly has received in recent years: Awards and Recognition ELI LILLY AND COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER	MINIMUM REQUIREMENTS: * Ph.D. degree in Toxicology, or a Ph.D., D.V.M., or M.S. degree in a related science with extensive training in the field of Toxicology * At least 3 years of on-the-job experience in safety assessment as it relates to the pharmaceutical industry * Excellent verbal and written communication skills * Demonstrates thoughtful leadership skills ADDITIONAL SKILLS/PREFERENCES: * Strong interpersonal and team-building skills, including demonstrated experience working in a team environment * DABT or other relevant certification * Study Director for GLP studies * Experience working on development teams consisting of ADME, biology, chemistry, regulatory, and medical * Subject Matter Expertise in Endocrine biology, Neurobehavior, or Biotherapeutics including a network of contacts in the scientific community * Regulatory experience, including Pharm/Toxicology experience at a regulatory authority OTHER CONSIDERATIONS: * Candidates with more years of experience are encouraged to apply, since final consideration for employment, compensation, and job responsibilities will reflect the experience level. * Some travel. * Office located in Indianapolis.	Indianapolis, Indiana	victoria.romera@lillyrecruiting.com	1/27/2012 6:13:47 AM
Details>>	Eli Lilly	Toxicological Pathologist (Job ID: 50436825)	Job Description: For more than 130 years, Lilly has been dedicated to meeting the health care needs of people in the United States and around the world. We address these needs primarily by developing innovative medicines—investing a higher percentage of our sales in research and development than any other major pharmaceutical company. If you are interested in being considered for employment with a “Best in Class” Pharmaceutical company, please review the following opportunity: Toxicological Pathologist Eli Lilly & Company is seeking a talented, curious and energetic veterinary toxicological pathologist with a minimum of 3 years experience working in the regulatory aspects of good laboratory practice drug development studies. The individual selected for this position should be able to work independently or in cross functional drug discovery and development teams within Lilly and with its external partners to provide scientific leadership in interpreting toxicity and pharmacologic effects caused by drugs in development. This person will have access to many technical specialty groups within Lilly and its external partnerships, and will be expected to design, conduct and interpret the clinical and/or morphologic pathology portions of studies, and to identify and bring resolution to pathology and toxicology issues affecting the development of pharmaceuticals. We are particularly interested in those pathologists who enjoy the challenges of problem solving and have experience representing issues to regulatory agencies. An experienced veterinary pathologist with strong communication and collaborative skills will be required to partner with a world-class organization of scientists in Investigative Toxicology, Molecular Pathology, and various drug discovery and development teams. KEY OBJECTIVES/DELIVERABLES: * Interpretation of pathology and toxicology data in primary discovery pathology reports and through active peer review of histopathologic sections and other pathology data in regulatory pathology reports from business partners; * Clear and concise, oral and written communication skills; * Development of scientific and regulatory perspectives on emerging issues and issue resolution plans and effective communication with Pathology and * Toxicology management representatives; * Development of target and molecule-based, risk mitigation strategies with drug discovery and development teams; * Representation of Lillys assets in partnership with Toxicology project leaders across multiple drug discovery and development teams; * Ability to travel to Lilly business partners and regulatory agencies to conduct Lilly Pathology/Toxicology business matters. Lilly credits its exceptional employees for its successes, and knows the key to ongoing achievement lies in attracting and retaining the best people. A company rich in heritage, Lilly employs individuals, conducts research and markets products worldwide. By providing for the unmet needs of our customers through a continuous stream of innovation, we will outgrow all competitors. Lilly earns consistent and wide recognition for creating an exceptional work environment while maintaining our highly regarded reputation in the Pharmaceutical Industry and Community. The following is a selection of awards and recognition Lilly has received in recent years: Awards and Recognition ELI LILLY AND COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER	MINIMUM REQUIREMENTS: * DVM and certification by American College of Veterinary Pathologists (ACVP)or European College of Veterinary Pathologists; * A minimum of 3 years in the regulatory aspects of good laboratory practice drug development studies; * Experience in designing and interpreting Preclinical Safety & Investigative studies; * Experience in representing pathology/toxicology issues to senior drug development management representatives. ADDITIONAL SKILLS/PREFERENCES: * PhD * Knowledge of biomarker identification and development	Indianapolis, Indiana	victoria.romera@lillyrecruiting.com	1/27/2012 6:11:48 AM
Details>>	Eli Lilly	Associate, Clinical Diagnostic Services - Fixed Duration Employee (Job ID: 50431759)	Job Description For more than 130 years, Lilly has been dedicated to meeting the health care needs of people in the United States and around the world. We address these needs primarily by developing innovative medicines—investing a higher percentage of our sales in research and development than any other major pharmaceutical company. If you are interested in being considered for employment with a “Best in Class” Pharmaceutical company, please review the following opportunity: Associate - Clinical Diagnostic Services – Fixed Duration Employee You will serve a pivotal role in study initiation, clinical trial execution, and providing medical, scientific, process, and logistic support as it relates to the management of the laboratory, ECG, imaging and other diagnostic support for clinical trials world-wide. You will coordinate vendor activities as well as facilitate research relating to laboratory, ECG, imaging and other diagnostic issues that arise during clinical trials. You will assist the medical staff in protocol development/ design and the review and monitoring of resultant data, ultimately providing high quality, combinable data in a cost effective and timely fashion. This is not a permanent position. It is for a Fixed Duration of up to 3 years. KEY OBJECTIVES/DELIVERABLES: 1. Team/Study Operational support * Assists medical staff in protocol development. * Provides technical expertise and diagnostic support of laboratory, ECG, imaging, sample storage for assigned compounds. * Works with Medical Quality Assurance and Legal as needed. * Prepares, coordinates and manages required documents for vendor services. * Establishes timelines and maintains to keep diagnostic services off critical path. * Contributes to vendor monitoring process. * Participates in diagnostic support training (Affiliate, Investigators, Study Coordinators, Clinical Research Organizations, etc). 2. Communication/information management * Maintains open line of communication with management, customers, and vendors to relay critical issues. * Provides metrics as requested. * Ensure customers understand CDS roles and responsibilities. Lilly credits its exceptional employees for its successes, and knows the key to ongoing achievement lies in attracting and retaining the best people. A company rich in heritage, Lilly employs individuals, conducts research and markets products worldwide. By providing for the unmet needs of our customers through a continuous stream of innovation, we will outgrow all competitors. Lilly earns consistent and wide recognition for creating an exceptional work environment while maintaining our highly regarded reputation in the Pharmaceutical Industry and Community. The following is a selection of awards and recognition Lilly has received in recent years: Awards and Recognition ELI LILLY AND COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER	MINIMUM REQUIREMENTS: * B.S. degree in medical technology, nursing or a related area. * At least 1 year of clinical laboratory or related experience * Experience in clinical trial environment. * Conceptual understanding of information technology. Maintain compliance with training requirements. * Experience with Microsoft Office and willingness to apply computer skills to other software. * Qualified candidates must be legally authorized to be employed in the United States. Eli Lilly and Company does not anticipate providing sponsorship for employment visa status (e.g.,H-1B status) for this employment position. ADDITIONAL SKILLS/PREFERENCES: * Strong self-management skills. * Strong teamwork and interpersonal skills. * Strong communication skills (verbal and written). * Organizational skills. * Negotiation skills. * Detail oriented. * Ability to handle multiple projects at one time. * Project management skills. OTHER CONSIDERATIONS: * Day shift with minimal travel. * Office environment.	Indianapolis, Indiana	victoria.romera@lillyrecruiting.com	1/27/2012 6:08:45 AM
Details>>	Eli Lilly	Principal Research Scientist PK/PD (Job ID: 50412280)	Job Description For more than 130 years, Lilly has been dedicated to meeting the health care needs of people in the United States and around the world. We address these needs primarily by developing innovative medicines—investing a higher percentage of our sales in research and development than any other major pharmaceutical company. If you are interested in being considered for employment with a “Best in Class” Pharmaceutical company, please review the following opportunity: Principal Research Scientist-PK/PD The Principal Research Scientist functions as a project leader in a multidisciplinary team environment with primary responsibility for the early preclinical development of antibodies and protein molecules. KEY OBJECTIVES/DELIVERABLES: * Integrate pharmacokinetics and PK/PD with discovery biology to define structure activity relationships to guide protein engineering strategies and to help optimize development of protein therapeutics. Interact across groups, including other departments, regulatory agencies, and functional groups within drug disposition. * Responsible for the design, conduct, interpretation and reporting of study results. * Design/execution of preclinical PK/PD studies * Develop and apply PK/PD modeling strategies * Write preclinical and clinical study reports * Interface with biology, toxicology and clinical research * Bioanalytical method development/validation. Lilly credits its exceptional employees for its successes, and knows the key to ongoing achievement lies in attracting and retaining the best people. A company rich in heritage, Lilly employs individuals, conducts research and markets products worldwide. By providing for the unmet needs of our customers through a continuous stream of innovation, we will outgrow all competitors. Lilly earns consistent and wide recognition for creating an exceptional work environment while maintaining our highly regarded reputation in the Pharmaceutical Industry and Community. The following is a selection of awards and recognition Lilly has received in recent years: Awards and Recognition ELI LILLY AND COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER	MINIMUM REQUIREMENTS: * Ph.D. in Pharmacokinetics/Pharmacodynamics or a related field in Pharmaceutical Sciences, with experience in PK/PD modeling. * 5 years of industry (Pharma/Biotech) experience with PK/PD modeling of monoclonal antibodies, peptides/proteins or fusion proteins. * Strong working knowledge of software such as WinNonlin, NONMEM and S-Plus. * Experience in the design and execution of PK/PD studies and development of mathematical PK/PD models. ADDITIONAL PREFERENCES: * Strong working knowledge of immunoassay methodology is desirable. * Experience with drug development and knowledge of regulatory processes preferred. * Prior experience working in an interdisciplinary team also preferred. * The ideal candidate will have demonstrated ability to identify scientific issues and solve problems, both individually and with partners in functional groups.	Indianapolis, Indiana	victoria.romera@lillyrecruiting.com	1/27/2012 6:05:42 AM