location_0_addressRegionName

location_0_addressCountryName

OFFSITE

UNKNOWN

ADAPTED_NOW

Toxicologist

ACTIVE

Location: Mountain View, California, , United States Posted: 2021-10-06 Position Title: Toxicologist Company Name: Trinity Consultants, Inc. Sector: Science Job Type: Full-Time SafeBridge Consultants, Inc., now doing business as SafeBridge Regulatory & Life Sciences Group, a wholly owned subsidiary of Trinity Consultants, Inc., is a unique resource for high level safety, health and environmental support to the pharmaceutical, chemical and biotechnology industries has an opening for a Managing Toxicologist. MANAGING TOXICOLOGIST Consider this special opportunity to join a high performing team of experienced consultants serving the occupational and environmental health and product safety needs of pharmaceutical, chemical and biotechnology companies across the country and internationally. You will fill a key senior position in providing risk assessment guidance and leadership to clients involved in the safe manufacture of potent new chemical entities and other toxic materials. Responsibilities will include providing occupational and environmental toxicology, risk assessment and regulatory compliance guidance to clients. Duties will include development of occupational toxicology documents such as: Occupational Exposure Limits (OELs), acceptable surface limits (ASLs), occupational health (hazard) categorizations (OHCs), and safety data sheets (SDSs). You will also be responsible for the development of product safety documents including permitted/ acceptable daily exposure (PDE/ADE) determinations for the prevention of cross-contamination from product residues impurities and other contaminants. You will also provide toxicology consulting support within your base of experience to clients as necessary and assist in project management, some marketing and client relations, as appropriate. You will be working with a senior team of recognized experts in toxicology, risk assessment, safety, industrial hygiene, environmental science and analytical chemistry. You will be responsible for both technical service and managing client accounts. SafeBridge offers a competitive compensation package and benefits including health care, life and disability insurance, 401(k) investment plan and a generous paid time off plan. Successful candidates for this position must have an MS/MA with a minimum of twenty (20) years of experience or a Ph.D. with fifteen (15) years of experience. DABT certification or equivalent is required. The ideal candidate has excellent interpersonal as well as written and verbal communication skills and is able to work on multiple projects while balancing changing priorities and deadlines. Experience in the pharmaceutical, chemical or biotechnology industries is a definite advantage. Health-based risk assessment, and project/personnel management experience will also be valued. PI149596250

Trinity Consultants, Inc.

JobTarget

Medical Science Liaison

With operations in 35+ nations and ~ 27,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment. CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma , one of the world's largest collectors of human plasma, which is used to create CSL's therapies. Seqirus is the second largest influenza vaccine company in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally. We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team! As a field-based medical expert, the MSL supports CSL Behring's products and therapeutic areas by advancing scientific and collaborative relationships and acting as a conduit for timely knowledge exchange with key members of external healthcare communities and internal stakeholders towards optimized patient outcomes. The MSL function in general is knowledge-based, anchored in educating internal and external stakeholders in the science behind, and safe and appropriate use of our products. The MSL supports the generation of medical-scientific knowledge and applies subject matter expertise and experience to special projects. This opportunity with our Coagulation and Respiratory team will entail a focus on the planning and implementation of medical-scientific knowledge exchange with coagulation and respiratory stakeholders. Responsibilities: <ul><li>Acquire and maintain a level of medical-scientific knowledge in the assigned therapeutic area(s) and/or disease state(s) related to CSL Behring's products. Accurately and compliantly interpret and disseminate balanced and factual scientific, clinical, and health economic data. Gather and evaluate new information as it applies to CSL Behring's products and areas of therapeutic interest.</li><li>Identify appropriate regional Key Opinion Leaders (KOLs) and Healthcare Professionals (HCPs) with which to develop professional relationships to ensure exchange of medical-scientific information relevant to CSL Behring's products and areas of therapeutic interest.</li><li>Deliver approved educational programs to relevant healthcare audiences (e.g. HCPs, Managed Care Organizations, Specialty Pharmacies, etc.).</li><li>Provide areas of interest and general high-level information regarding CSL Behring's Investigator Study (IIS) Program process in response to unsolicited requests. Monitor and communicate progress for those IISs approved and supported.</li><li>Gather, translate, and communicate actionable, strategy-aligned insights from scientific, educational, and conference setting interactions</li><li>Attend scientific and medical meetings.</li><li>Deliver approved educational programs and training to relevant internal functions.</li></ul> Qualifications: <ul><li>Doctoral level degree in a Medical and/or scientific field is preferred. </li><li>Degree in a Medical and/or scientific field with strong relevant experience will be considered.</li><li>Minimum of 3 years in the pharmaceutical industry or healthcare experience is required.</li><li>Prior MSL experience is required.</li><li>Must be able to organize, prioritize, and work effectively in a dynamic, field-based environment. </li></ul> #LI-JG1 Worker Type: Employee Worker Sub Type: Regular

CSL Behring

Medical Science Liaison, Coagulation (Central North)

Bayard Advertising

Research Associate

US-CA-San Diego ID: 2020-1358 Category: Research & Development Overview AlivaMab Discovery Services, LLC (ADS) is recruiting for an outstanding individual with a range of skill sets supporting the successful discovery of fully human antibody drug candidates from the AlivaMab ® Mouse platform. This candidate should be a motivated team player, able to wear multiple hats while working in an exciting, fast-paced environment, working to discover the next generation of breakthrough antibody drugs. Led by personnel with combined decades of experience in therapeutic antibody drug discovery and development, AlivaMab Discovery Services continues expanding its services in therapeutic antibody drug discovery in support of the biotech and pharma communities. You will be a key contributor in a team dedicated to delivering best-in-class therapeutic antibody candidates that will improve outcomes for patients. Responsibilities Responsibilities Your primary responsibilities will be in the area of animal immunizations, hybridoma generation, tissue culture, and antibody screening by ELISA, FACS, and functional assays. You will be executing and delivering for projects and preparing written reports. We are looking for independent and creative researchers that demonstrate initiative, who are capable of experimental design and execution, including troubleshooting. You will work closely with other team members and leaders. You will be able to effectively present and communicate concepts and results, both orally and in writing, to management and clients. Qualifications Key Skills and Requirements: <ul><li>B.S., M.S., or PhD degree in life sciences or related discipline with three or more years' directly relevant experience</li><li>Impeccable cell culture and sterile technique is essential for success in this role</li><li>Ability to efficiently work in team-based environment on challenging drug discovery projects requiring high throughput cell culture and screening </li><li>Experience in multiple antibody screening assay methods (ELISA, FACS, Octet, functional assays) </li><li>Experience performing cell-based functional assays to identify functional antibody candidates. Functional assay development/optimization experience a plus </li><li>Prior experience in small animal immunizations with recombinant proteins, cells and DNA (HDTVI experience strongly desired) for the discovery of therapeutic antibody drug candidates</li><li>Excellent organization in day to day experiments and timely updating of experiment files</li><li>Proficiency in Microsoft Office Suite (Word, Excel and PowerPoint) and Graphpad Prism</li><li> Nice to have: previous experience in stable cell line generation, hybridoma fusions, FACS sorting, protein purification/characterization and general molecular biology skills </li></ul> AlivaMab Discovery Services provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, gender identification, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. PM18 #LI-DNI PI147398516

AlivaMab Discovery Services

Senior Research Associate/Scientist: Antibody Discovery

Medical Laboratory Technician

Job Summary: Ensures quality specimens for laboratory testing. Operates system / methodologies in order to produce timely and accurate test results for patients, QC, and proficiency testing. Reports clinical data accurately and efficiently so that caregivers receive timely patient information. Participates in growth opportunities to enhance personal, team and departmental development License, Certification, Education or Experience: REQUIRED for the position: • MLS (MT) (ASCP) or equivalent certification in good standing required. • Bachelor of Science and completion of an accredited laboratory science programDESIRED for the position: Molecular experience preferred •One year experience in a clinical hospital laboratory preferredThis position is covered by a collective bargaining agreement between EvergreenHealth and the United Food and Commercial Workers (UFCW), Local 21. PM21 PI147491102

EvergreenHealth

Medical Lab Scientist-Non Contract UFCW

Scientist

Perform high quality clinical data review and identify clinical data insights through ongoing patient level review and trends analysis, thereby supporting for example Interim Analysis, Database and Post Lock activities and resolution of scientific & medical issues throughout the study lifecycle. For all these tasks, work in close collaboration and alignment with clinical development lead. Ensure all questions / issues requiring medical oversight are brought to the attention of the clinical development lead. Work to improve the quality of reviews/ insights with an emphasis on subject safety and eligibility, data integrity, trend identification, analysis and remediation, and identification of cases for medical review. Contributes to the Data Review and data review strategy, ensuring that protocol-level deviations, eligibility criteria, study assessments & other aspects of the protocol are implemented consistently across the study (across countries/ sites). This could also include support for Case Report Form (CRF) development, and implementation of data capture tools. Contribute to the development of the clinical protocol. Also contribute to the identification, formulation and implementation of amendments to the clinical protocol, in close collaboration with clinical lead. Provide insights to and facilitate data review process improvements, for example by identification of redundant reports, implementation of innovative data analysis processes and tools, and their continuous improvement. Contribute to the creation of study-level documents, including preparation of clinical sections of key regulatory documents, such as Investigator’s Brochures, briefing books, safety updates and submission dossiers.  Contribute to the review and writing of clinical trial documents for study CSR activities, and publications (if applicable). Support pharmacovigilance activities (e.g. contributing to aggregate reports, patient narratives, attendance of pharmacovigilance monitoring meetings) Support regulatory activities, like preparation and conduct of meetings with regulatory agencies. Produce training materials, share best practices and provide training to the broader clinical trial teams. Support preparation and (if applicable) participate in study level meetings for example Investigator Meetings, Data Monitoring meetings, and others. Knowledge, Skills & Abilities Advanced degree in life sciences/ healthcare (or clinically relevant degree) is required. Master’s, PharmD, MPharm, PhD, MBBS, CompanyS, MD strongly preferred. 2 years+ scientific, strategic and operational experience in planning, executing, reporting and/ or publishing clinical studies (pharmaceutical industry or academia) Good knowledge of procedures in global clinical studies in a pharmaceutical company or contract research organization (CRO), or comparable experience within academic research institution. Strong familiarization with Good Clinical Practice (GCP) and drug development processes, ideally Phase 1 – 3; ideally paired with experience in Oncology / Immuno-Oncology   Knowledge of principles of clinical data collection and reporting; demonstrated ability to use systems and tools (e.g., EDC systems, Excel, etc.) for data collection, analysis and reporting. Ideally first experiences in how to improve and accelerate processes, systems and tools and drive continuous improvement. Experience in RDC is an advantage. Experience to work in a matrix, ability to influence without authority High flexibility and adaptive working style, ability to work on several tasks at the same time Ability to work effectively under high time pressure, while maintaining high quality standards Ability to effectively prioritize tasks, and implement accordingly High proficiency in English (written and spoken); German a plus

Biontech

Clinical Scientist, Drug Development

Ivy Exec

Data Scientist

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants. Description Role will work on but not limited to:
<ul><li>Building data ingestion pipelines</li><li>Cleaning up and enriching data using transformation layers</li><li>Creating informative, visually interesting dashboards and reporting</li><li>Developing predictive models</li><li>Performing cross-department ad-hoc analysis</li><li>Sharing insights and teachings with non-Analytics team members</li></ul><ul><li>Education in a quantitative field including computer science, statistics, mathematics, finance or accounting</li><li>Experience using data science skills and quantitative analysis to solve business problems</li><li>Comfortable communicating analysis to members of the executive team or external stakeholders using tools like SQL, Python, etc.</li><li>Capable of deriving analytics across many platforms (Jupyter, Excel, Looker, etc.)</li></ul>Excellent opportunity within a publicly traded alternative medicine company in Chicago to join a highly acquisitive business currently in growth mode. <ul><li>Amazing Big 4 Sr Leaders/Mentors</li><li>Highly acqusitive publicly traded company</li><li>Unlimited PTO</li><li>C- Suite exposure and high impact opportunity driving business decisions </li></ul>

Michael Page is one of the world's leading professional recruitment consultancies, specializing in the placement of candidates in permanent, contract, temporary and interim positions with clients around the world.
The Group has operations in the Americas, UK, Continental Europe, Asia-Pacific and Africa. 
In the US, we focus on the areas of:
<ul>
<li>Advisory</li>
<li>Banking and Financial Services</li>
<li>Finance and Accounting</li>
<li>Engineering and Manufacturing</li>
<li>Healthcare & Life Sciences</li>
<li>Human Resources</li> 
<li>Information Technology</li>
<li>Legal</li>
<li>Marketing</li>
<li>Page Personnel Office Support</li>
<li>Oil and Gas</li> 
<li>Procurement and Supply Chain</li>
<li>Real Estate and Construction</li>
<li>Sales</li>
</ul>

Michael Page

Data Scientist | Chicago | Alternative Medicine

recruitics_michael page

Employee Referral Program

Maternity/Paternity Paid Leave

Medical, Dental and Vision

Paid sick days

Vacation/paid time off

INTEGRATED

Spherion, in partnership with Exact Sciences, is actively recruiting for multiple part-time Clinical Laboratory Scientists to join their collaborative and innovative team. This position performs laboratory analysis on clinical specimens using established laboratory procedures under the direction of the Laboratory Medical Director. As a Clinical Laboratory Scientist, you are responsible for recognizing and resolving problems using good laboratory practices. This temporary role is estimated to last 3-6 months based on business needs. Multiple shift options are available and will be discussed during the interview process. $1,500 bonus given after 6 months or at the completion of the contract!! Responsibilities: - Perform moderate, and/or highly complex analytic processes without direct supervision. Interpret problems with specimens that meet the rejection criteria for unacceptable samples. Make the decision to reject a sample and request recollection to ensure the validity of results - Operate laboratory instruments and ensure the proper functioning of laboratory equipment - Complete and document required maintenance activities on equipment, recognize and elevate potential issues reporting service needs to leadership for resolution - Perform quality control procedures as specified and maintain quality control records and documentation necessary to meet the standards of accrediting agencies - Understand appropriate specimen collection, handling, and transport procedures - Prepare specimens for analysis and determine the acceptability of samples within guidelines - Assists in developing procedures for specimen collection, handling, and transport to maintain specimen integrity and viability - Validate the acceptability of test results by reviewing test parameters - Identify the technical, instrumental, and/or physiologic causes of unexpected test results - Monitor quality assurance and assist in data collection and preparation of QA indicators - Perform internal and external proficiency testing. Handle proficiency testing samples in the same manner as patient samples - Maintain a clean and orderly work area. Clean bench surfaces and equipment each shift or after contamination or spill - Meet work product output expectations maintaining all section turn-around times - Participate in continuing education and staff meetings. Prepare and presents continuing education programs for department personnel as requested - Apply step by step thinking, problem-solving, and critical thinking patterns - Contribute to design, research, review, and writing of laboratory manuals. Remain informed of procedure updates and changes - Comply with safety and hazard regulations as outlined in the Clinical Laboratory Safety Manual. Understand, maintain, and enforce safety guidelines - Observe principles of data security and patient confidentiality. Maintain ethical standards in the performance of testing and in interactions with patients, co-workers, and other health care professionals - Support and comply with the companys Quality Management System policies and procedures Working hours: Various Shifts Available Skills: - Demonstrate adaptability by embracing changes in the laboratory with a positive attitude - Ability to lift up to 40 pounds for approximately 25% of a typical working day - Ability to work seated for approximately 50% of a typical working day. Ability to work standing for approximately 50% of a typical working day - Ability to work in front of a computer screen and/or perform typing for approximately 75% of a typical working day - Ability and means to travel 5% between Madison Laboratory locations - Ability to comply with any applicable personal protective equipment requirements Education: Bachelors Experience: 1-4 years Qualifications:

<h4>WE'RE SPHERION. OUR VISION IS TO DRIVE CAREERS, GROW BUSINESSES, AND BETTER THE COMMUNITIES WE CALL HOME.</h4>
 
<h4>We're a national recruiting and staffing enterprise that blends the resources of a global HR company with the local insights of our independent franchise owners. A pioneer in the staffing industry, we’ve been providing companies with the workforce solutions they need for over 75 years, while helping people find jobs and build careers where they can thrive.</h4>

Spherion

Clinical Laboratory Scientist

ONSITE

FULL_TIME

YEAR

Laboratory Scientist

Qualifications<ul><li>Broad knowledge of and experience applying the principles and theories of molecular and cell biology, pathophysiology, immunology, biochemistry or biotechnology in addition to skills specifically required for performing and directing independent research.</li><li>Knowledge of and experience with the safe handling of hazardous materials including blood products and other bodily fluids, infectious agents, toxins, organic solvents, radioactive substances, and carcinogens by incumbent and assigned personnel.</li><li>Knowledge of and previous experience with collaborative research/technology transfer agreements with military and civilian scientific/medical organizations is a plus.</li><li>Previous experience with effectively organizing and managing multiple projects that are operative concomitantly, including the management of work schedules and assignments of available technologists and instrumentation.</li><li>Must have highly developed and diverse laboratory skillset, with experience conceptualizing and developing novel research questions for writing/co-writing human use or laboratory research protocols.</li><li>Knowledge of and experience with the development and submission of formal written research protocols and projects to include funding proposals: assessment of the cost/benefit ratio of conducting research, considering both the material costs and the man-power investment.</li><li>Experience and skill preparing manuscripts for publication in scientific journals.</li><li>Excellent oral communication skills and experience making presentations at scientific meetings, consulting with investigators and scientists in pertinent areas of expertise, and instructing technicians and other investigators.</li><li>Knowledge of and experience with identifying varied internal and external sources of funds and materials to support laboratory and clinical research.</li><li>Knowledge of and experience with assisting in the formulation of experimental hypotheses and with designing and implementing protocol-driven research proposals, animal use protocols, human use protocols, technical reports, final reports and peer reviewed manuscripts.</li><li>Experience collecting, processing and interpreting data sets.</li><li>Experience developing presentation materials, Standard Operating Procedures, and presenting findings at technical and professional meetings.</li><li>Experience with preparing experimental subjects, setting up experimental equipment, and aiding in the training and development of experimental subjects for experimental procedures.</li><li>Experience serving as Principal Investigator or Associate Investigator for research projects.</li><li>Experience identifying and seeking sources of funding or procurement of research materials through writing/co-writing grant proposals, technology transfer agreements and data transfer agreements with industry and/or academia.</li><li>Experience with preparing manuscripts and presentations including performing literature reviews, writing of manuscripts, preparation and selection of appropriate graphical arts, selection of appropriate journals for manuscript submission, and defense of the submitted manuscripts.</li><li>2-3 years of post-doctoral experience (minimum)</li></ul>Education/Certification Requirements<ul><li>Doctoral in a biological discipline of Cancer Biology, Molecular Oncology, and/or Molecular Medicine</li></ul>Work Environment & Other Information<ul><li>Location: San Antonio, TX</li><li>Criminal, Driving, Education, and Employment Background Check Required.</li></ul>

zCore Business Solutions

Biomedical Laboratory Scientist

monster

<DIV>Job: Medical Laboratory Scientist/ MLS Duration: 13 Location: Pueblo, COJob Description: Required: Bachelors Degree in a related laboratory field and Medical Laboratory Scientist (MLS) registered with the American Society of Clinical Pathologist (ASCP). Benefits : Sign on Bonus + Completion Bonus</DIV>

vTech Solution Inc.

Medical Laboratory Scientist

vTech Solution Inc

Medical Scientist Jobs | Monster.com