location_0_addressRegionName

location_0_addressCountryName

ONSITE

FULL_TIME

ADAPTED_NOW

YEAR

Biostatistician

ACTIVE

THE COMPANY PHASTAR is a multiple award-winning, top 10, data focused CRO specializing in providing statistics, programming, data management and data science services. With offices across the US, UK, Germany, Kenya, Japan and Australia, PHASTAR is a global CRO that is continuing to grow. In 2019, PHASTAR won the prestigious Queen’s Award for Enterprise, following our impressive growth from a one-person operation to a global CRO within a decade. Our unique approach to data analysis, “The PHASTAR Discipline”, has led us to build a reputation for outstanding quality. With this as our core focus, we’re looking for talented individuals who share our passion for quality and statistical expertise to join our team. THE ROLE As a Principal Biostatistician, you will hold a combined project leadership and hands-on technical statistics role. Working across a range of phases and therapeutic areas, you will lead assigned studies, ensuring they are delivered to optimal quality, on time and on budget. Key Responsibilities:<ul><li>Lead a team of statisticians and programmers to manipulate, summarise and analyse clinical trial data using a variety of statistical methods</li><li>Project manage assigned studies including allocating staff, predicting and planning resources</li><li>Prepare and review study documentation including protocols and statistical analysis plans</li><li>Advise, mentor and teach internal and external statisticians with regards to statistical and data analysis methods</li><li>Function as a study expert across multiple studies, helping to clarify details on analysis methods for the internal PHASTAR team</li><li>Ensure the team meets the highest quality standards and follows the principles detailed in PHASTAR’s internal procedures</li><li>Maintain a positive and engaging client relationship with regards to statistical issues</li></ul> SKILLS AND EXPERIENCE REQUIRED <ul><li>PhD or MSc in Biostatistics or related discipline</li><li>Experience working within a clinical trials environment (CRO, pharma or academic)</li><li>Previous experience performing statistical analysis using SAS</li><li>Excellent written and verbal communication skills</li><li>Ability to communicate with a broad range of people across different functions</li></ul> WHY PHASTAR This is a unique opportunity to join a company where hard work and fun coincide! We offer structured training and development plans, the opportunity to continue your own research, a competitive salary, an excellent benefits package, and flexible working arrangements, all within a relaxed and friendly working environment where fun is encouraged and renowned social events are organised throughout the year. Should you feel that you have the right skill set and motivations for this position, please apply! Please note that we are considering candidates located in any US state as this role can be carried out remotely. ***PHASTAR does not accept any CVs received from recruitment agencies. In the event that speculative CVs are submitted by recruitment agencies, PHASTAR reserves the right to contact these candidates directly and consider them for current/future vacancies without any financial obligation to the recruitment agency in question. This applies to any CVs sent directly to any PHASTAR employee.***

PHASTAR

Remote Principal Biostatistician (Ref: RM)

monster

401K

Employee Events

Employee Referral Program

Flexible Spending Accounts

Gym Memberships

Life Insurance

Maternity/Paternity Paid Leave

Medical, Dental and Vision

Military Leave

On Site Cafeteria

Paid Holidays

Paid sick days

Parking 

Professional Development

Retirement / Pension Plans

Tuition Reimbursement

Vacation/paid time off

OFFSITE

UNKNOWN

Research Associate

<h2>Position Summary</h2>Odyssey Systems has an exciting new opportunity for a Research Associate supporting the WRAIR – Department of Diarrheal Disease Research (DDR).  Diarrheal diseases, notably Shigella, are a major source of morbidity among deployed U.S. military and a significant threat to readiness. To that end, BDB aims to develop a safe and effective vaccine against multiple Shigella strains to protect personnel overseas and keep Soldiers in the fight. This position is perfect for a recent college graduate who is interested in getting great training from a top notch team. <h2>Responsibilities</h2>Duties include, but not limited to: The Research Associate will provide support in the areas of immunological research to include: <ul><li>Conducting bench research on Shigella (or other enteric pathogens) to include large scale production of purified proteins and LPS, immunogenicity, biochemistry and mechanisms of action of Shigella subunit vaccines or live Shigella vaccine candidates.</li><li>Assisting in the evaluation of Shigella vaccines in clinical and pre-clinical studies to include immunizing small animals, collecting blood, lymph nodes mucosal washes, and determining the immune response elicited after vaccination using cellular proliferation, antibody secreting cell (ASC), ELISA, and immunobead multiplexing assays.</li><li>Assisting in pre-clinical evaluation of prototype diagnostic devices for detection of Shigella and other enteric pathogens from complex biological matrices such as stool.</li><li>Assisting in the daily maintenance and operations of the lab to include media preparation, glassware and hazardous waste management, and administrative duties such as ordering supplies and periodic lab inventories.</li><li>Establishing and/or developing laboratory procedures and analyze and/or evaluate research data; participate in a cooperative effort to accomplish goals of the laboratory; maintain proficiency and expertise in the field of research.</li><li>Utilizing professional knowledge of: theories, principles, methods, and techniques of immunology, cell biology, and microbial pathogenesis, such as ELISA, ASC assays, cellular proliferation assays, western blotting, cell culture, small animal handling (such as mice or guinea pigs), and aseptic technique. </li></ul> <h2>Qualifications</h2>Minimum Qualifications:<ul><li>Bachelors Degree in a scientific discipline is required</li><li>Recent college graduate with exposure and interest in immunology </li><li>Willingness to work with small animals in a lab environment required</li></ul>Preferred Qualifications:<ul><li>Familiarity with the following research equipment is preferred but not required: HPLC, PCR, Mass spectrometer, Flow Cytometers, cell counters, cell separation devices, fermenters, lyophilizes, peptide synthesizers </li><li>Familiarity with the following typical procedures is preferred but not required to: gel electrophoresis, protein assays, fermentation and purifications, and immunological functional assays.</li><li>Familiarity with Microsoft Excel, Microsoft Access, Prism and SAS.</li></ul>Additional Information: <ul><li>US Citizenship required</li></ul>#LI-AW1<h2>Company Overview</h2>Odyssey Systems Consulting Group, is an innovative small business committed to providing world-class technical, management, and training support services to government and public sector clients. We focus on people, processes, and performance to deliver superior results. Since our inception in 1997, our commitment to mission success and customer satisfaction has been recognized with exponential growth and exceptional past performance ratings. We accept challenging assignments and drive projects from the planning stages, through implementation, and into operations and support. Please note: Final compensation for this position will be determined by various factors such as the Federal Government contract labor categories and contract wage rates, relevant work experience, specific skills and competencies, geographic location, education, and certifications. Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

Established in 1997, Odyssey Systems Consulting Group, Ltd. is a leading provider of management, analytical, and technical support services for government and private-sector customers. Odyssey delivers innovative solutions in response to complex and challenging customer requirements.
Our portfolio of successful projects demonstrates our ability to efficiently plan, staff, and manage efforts of all scopes and sizes. Our employees provide tailored functional expertise in technology, engineering, and management principles. We offer vast experience in acquisition strategy development and document generation; source selection support; cost, schedule, and performance management; systems engineering and analysis; risk management; cost/benefit and earned value analysis; computer-based training development; communication planning and operations; and lifecycle sustainment and product support. Odyssey also offers research and acquisition support services to the DoD medical domain, leading DoD medical mission support through several prime services contracts.
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A six-time Inc. 5000 honoree, Odyssey has earned recognition on the 2019 Inc. 5000 as one of the most successful companies in America. In Inc.’s annual guide to the 5,000 fastest-growing privately held companies in the U.S., we were ranked #162 in the Government Services category, delivering a wide range of services to DoD customers and beyond.
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Odyssey Systems Consulting Group, Ltd.

Research Associate – Immunology

 Odyssey Systems Consulting Group

TEMPORARY

CONTRACTOR

HOUR

A client of Sharp Decisions Inc. is looking to bring on a Senior Research Associate to be based in Santa Monica, CA. Position does require the resource to be onsite 3-5 days a week. Position is on a one year contract basis with possible extension. *W2 and Local only. Please note this is routine testing role where they are testing samples on a regular basis and producing data. Preferred: experience with ELISA and cell culture Requirements: experience with MS Suite and Sharepoint Job Description Client is seeking a highly motivated individual with analytical development and support experience to work on innovative T cell therapy for cancer treatment. The Senior Research Associate of Analytical Development (AD) will be mainly responsible for deep analytical characterization of cell therapy products at different developmental stages and oversee the maintenance of analytical instruments. You will also be assisting in planning and executing laboratory studies, analyze/review experimental data and carefully document resultant information. This position reports to a Manager. Responsibilities (include but are not limited to):<ul><li>Proficiently execute cell-based assays on a regular basis or as needed, in support of process development and product characterization</li><li>Perform data analysis, data reporting, and further statistical analysis with advanced analysis software</li><li>Assist in data verification to ensure data integrity</li><li>Maintain and operate plate readers including VersaMax and SpectraMax</li><li>Perform reagent lot and assay control qualifications</li><li>Transfer cell-based assays from the method development group to analytical testing group</li><li>Review and maintain standard operating procedures and analytical test methods</li><li>Develop electronic templates for documenting assay execution</li><li>Maintain and handle human cell lines: thaw, culture/expand, and cryopreservation</li><li>Write, review and edit accurate technical documents</li><li>Assist in developing, qualifying, executing and documenting cell-based methods to study and characterize processes for production of T cell therapies</li><li>Provide user training on instruments, sample analysis, and cross-train analysts on analytical methods</li><li>Coordinate activities for members of project teams in the initiation and execution of laboratory experimentation</li><li>Participate in sampling and study plan meetings to support different functional areas within Process Development</li><li>Additional responsibilities may be assigned to reflect changes in business processes.</li></ul>Qualifications<ul><li>BSc degree with 2 plus years industry 'hands on' experience in cell therapy areas. Open to candidates with a Masters with 1 year of relevant work experience</li><li>Demonstrated strong knowledge of developing cell-based assay, and technical knowledge of instrument & software, and method controls</li><li>Proficient in operating equipment such as VersaMax and SpectraMax</li><li>Understand deep characterization knowledge in patient materials, product knowledge, and process characterization</li><li>Demonstrates emerging ability in developing methods, techniques and evaluation criteria for obtaining results and interpreting experimental outcomes</li><li>Ability to follow laboratory procedures with attention to detail, and successfully execute experiments at the bench</li><li>Ability to think critically, demonstrate troubleshooting and problem solving skills</li><li>Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment</li><li>Previous experience with other technologies is a plus</li><li>Excellent skill in Microsoft word, Excel, MS Teams, and SoftMax Pro analysis software</li></ul>Comfortable working in a fast-paced company environment with minimal direction and able to adjust workload/assignments based upon changing priorities<ul><li>Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of initial job description</li></ul>

For over two decades, Sharp Decisions has provided superior, award-winning service in strategic business and technology consulting services to government agencies at all levels, as well as domestic and global corporations. With subject matter expertise in Investment Banking, Finance, Healthcare, Media &#38; Telecommunications, and Manufacturing, Sharp Decisions is well equipped to serve your needs.

Established in 1990 with headquarters in New York City, and locations in Princeton, Charlotte, Los Angeles, Phoenix, Europe and Canada, Sharp Decisions has been the technology backbone for a client portfolio that includes an array of well-known companies. As a Certified Woman-Owned Business Enterprise and approved vendor, Sharp Decisions offers a powerful, cost-effective advantage. We actively partner with other MBEs to add value and meet diversity program requirements.

Sharp Decisions is also committed to hiring and training post-9/11, tech-savvy U.S. armed forces veterans through our V.E.T.S.â„¢ (Vocation, Education and Training for Service members) Program, but we cannot do it alone. Companies like EmblemHealth, Freddie Mac and Experian have stepped up to bring aboard our highly qualified and skilled veterans. We need more companies like them to take a stand and bring our veterans aboard. Our clients have told us that our veterans are more effective than their college hires because two weeks on the job for them equates to 2-3 years of experience! Learn more at www.sharpdecisions.com/vetsprogram.

Sharp Decisions

Senior Research Associate (W2 and Local Only)

NONE

applyType not onsite or offsite:ApplyRequestDto(applyUrl=null, applyType=NONE, resolvedRedirectUrl=null, onsiteApplyEmail=null)

<a href="http://www.dallasnews.com/jobs/" rel="nofollow nofollow noopener noreferrer" target="new"><img src="http://www.dallasnews.com/images/gbl_listinglogo.gif"/></a> <table border="2"><tbody><tr><td><table><tbody><tr><td><dl><dd>Research Associate 2</dd><dd>Baylor Research Institude</dd><dd>Dallas, TX</dd></dl></td></tr></tbody></table><dd>Plan/execute lab experiments re orthopedic diseases in hip, pelvis, & spine. Req. Doctor of Medicine in Orthopedics; req. 60 mos exp. in Orthopedics, Surgery or Research; req. </dd><dd>2 yrs. exp. in the following: </dd><dd>orthopedic surgery research; morphologic measurements in imaging studies of the hip, pelvis, & lumbar spine; prep, writing, & submitting sci. articles </dd><dd>/book ch; perform peer-review assessments for medical journals; prep. lectures to medical prof in orthopedic area; exp. may be gained concurrently. Mail resume to Michelle Hopkins, Baylor Research Institute, 3434 Live Oak St., Dallas, TX 75204. Position based in </dd><dd>Dallas, TX. EOE. </dd></td></tr></tbody></table> The Dallas Morning News  -  10/24/2021

Baylor Scott & White Research Institute

Research Associate 2

PROGRAM DESCRIPTION The Laboratory Animal Sciences Program (LASP) provides exceptional quality animal care and technical support services for animal research performed at the National Cancer Institute at the Frederick National Laboratory for Cancer Research. LASP executes this mission by providing a broad spectrum of state-of-the-art technologies and services that are focused on the design, generation, characterization and application of genetically engineered and biological animal models of human disease, which are aimed at the development of targeted diagnostics and therapies. LASP contributes to advancing human health, developing new treatments, and improving existing treatments for cancer and other diseases while ensuring safe and humane treatment of animals. KEY ROLES/RESPONSIBILITIES <ul><li>Management and execution of numerous, concurrent research studies utilizing nonhuman primate (NHP) models</li><li>Managing protocol schedules to achieve successful experimental conduct while maximizing the use of staff/facility resources</li><li>Monitoring NHP animal study protocols to ensure compliance with ACUC approved procedures and animal numbers</li><li>Performance of specialized experimental procedures utilizing nonhuman primates including administration of drugs, pre-surgical preparation, minor surgical biopsies, BAL, bone marrow collection, anesthesia monitoring, post-surgical care</li><li>Drafting animal study proposals and modifications to support ongoing and new research endeavors</li><li>Observing and recording physical signs of nonhuman primate health and record data</li><li>Maintaining a proper living environment for nonhuman primates including enrichment, behavioral assessment, social housing and training</li></ul> BASIC QUALIFICATIONS <ul><li>Possession of a Bachelor's degree from an accredited college/university in a field related to biomedical research or four (4) years equivalent experience in the appropriate field in lieu of degree. Foreign degrees must be evaluated for U.S. equivalency</li><li>In addition to educational requirements, a minimum of two (2) years progressively responsible job-related biomedical experience</li><li>Must be able to function independently in an animal research facility environment, and in support of investigators engaged in animal research</li><li>Previous experience in handling nonhuman primates in a research facility including a variety of experimental procedures</li><li>Ability to multitask, coordinate protocol schedules, and perform a variety of technical procedures on nonhuman primates</li><li>Ability to maintain precise, accurate records</li><li>Knowledge of standard operating procedures for animal facilities and the basic requirements for maintaining laboratory animals and performing scientific procedures involving animal testing and data collection</li><li>Computer and writing skills</li><li>Must participate in the occupational health program, medical health screenings, and similar.Must understand that the position has the risk for exposure to zoonotic agents as well as other hazardous agents or chemicals</li><li>Ability to obtain and maintain a security clearance</li></ul> PREFERREDQUALIFICATIONS Candidates with these desired skills will be given preferential consideration: <ul><li>Excellent observation and organization skills</li><li>Experience in performing surgical procedures on NHPs</li><li>Basic necropsy techniques</li><li>Excellent written and oral communications skills</li><li>Experience with other laboratory animal species including mice, rats, and aquatics</li></ul> JOB HAZARDS <ul><li>This position is subject to working with or have potential for exposure to animal(s) and/or animal material(s)</li><li>This position is subject to working with or have potential for exposure to infectious material, requiring medical clearance and immunizations</li><li>This position is subject to atmospheric conditions that would require the usage of a respirator, requiring a medical clearance</li><li>This position is subject to working in or have the potential to exposure to high noise levels for extended periods of time requiring medical clearance</li><li>This position is subject to the environmental conditions such as working outdoors, high humidity areas indoors, dampness and chilling, dry atmospheric conditions, etc. as part of the job</li><li>This position is subject to working with radioactive material and requires to become an approved radiation worker</li></ul>

Frederick National Laboratory

Research Assoc I (req1702)

Shaker_PX

INTEGRATED

https://www.youtube.com/watch?v=aV0cEhLLbi4

job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treatments streamlined, easily accessible, and globally produced. If you share their goal of approaching healthcare in a novel way, look no further - apply for your dream job now!  location: New York, New York job type: Contract salary: $28.63 - 33.68 per hour work hours: 9 to 5 education: Masters   responsibilities: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.This position will support the global medical and scientific Lyme disease vaccine team by developing and organizing the scientific knowledge base through data analysis and interpretation, application of the Epidemiology literature, and interaction with internal and external experts. Specifically, the candidate in this position will analyze US and EU surveillance data, review local Epidemiology data to quantify burden of disease, systematically organize global Epidemiology data in a centralized hub, and support on-going Epidemiology burden of disease studies.The candidate must have completed graduate training in Epidemiology with an understanding of statistics and programming as the candidate will be expected to conduct analyses. The candidate must be able to synthesize the literature and develop strategies to quantify the burden of disease. Finally, the candidate must have exceptional organizational skills and attention to detail. Understanding how to present and convey complex information visually through slides is a plus.  qualifications: 			 Master of Public Health or Master of Science in Epidemiology  skills: Epidemiology Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Randstad was founded in 1960 by Frits Goldschmeding. We've never let go of his passion or the values that he established. By staying true to those fundamentals, we've expanded to represent more than 90 percent of the HR services market.We provide outsourcing, staffing, consulting and workforce solutions within the areas of engineering, accounting and finance, healthcare, human resources, IT, legal, life sciences, manufacturing and logistics, office and administration and sales and marketing. We can’t wait to tell you all about it.Our mission is to be a world leader in matching demand for, and supply of, labor and HR services. We believe in the value of work as a unifying force that shapes society for the better. We live by the core values established early in our company's history: to know, serve and trust, striving for perfection and simultaneous promotion of all interests.

Randstad USA

Randstad Life Sciences

<div class="section-data">If you are a Research Associate with experience, please read on! 
We are an clinical stage biotechnology company working on engineered antibodies for multiple therapeutic applications. We are a fully funded publicly traded company with great benefits and growing staff.</div><h4 class="section-title">What You Will Be Doing</h4><div class="section-data section-data-title">You will be working on support for protein production research to drive the pre-clinical pipeline of our company with a focus on utilizing automated high throughput workflows. You will work with Scientists to optimize processes to meet our specific project needs and to improve the quality and throughput. You will make sure that you are effectively documenting results and providing clear communication of data in Group Meetings, Project Team Meetings, and other forums.</div><h4 class="section-title">What You Need for this Position</h4><div class="section-data section-data-title">- BS degree in Biology, Chemistry or similar - 3+ years of industry experience supporting automated laboratory process development 
- 2+ years of hands-on experience with liquid handlers (Hamilton, Tecan, Beckman, or Agilent) preferred 
- Experience with mammalian protein expression/purification is a bonus</div><h4 class="section-title">What's In It for You</h4><div class="section-data section-data-title">- Medical, dental, and vision 100% paid for you and dependents by us - STD, LTD, Basic Life and AD&D Insurance, Supplemental Life and AD&D insurance 
- FSA 
- 401k 
- PTO 
- Cell phone & internet subsidy 
- Annual bonus program 
- Stock options</div><div class="section-data">So, if you are a Research Associate with experience, please apply today!</div>

CyberCoders, a division of ASGN, is a leading permanent placement recruiting firm. Through our innovative technology and efficient recruiters, CyberCoders helps find the right candidate fast.
Founded in 1999, CyberCoders is built on a success oriented culture. Above all – we know both candidates and clients want quality and they want it now. No other recruiting firm can offer Cyrus, our proprietary technology built to search smarter and quicker, matching the best applicant to the right job.

CyberCoders

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Research Associate II – Labcorp Drug Development (Ann Arbor, MI). Interpret protocols for preclinical oncology research & use small animal surgical, imaging & adv radiotherapy techniques for preclinical oncology research. Must have bachelor’s or equiv in Biological Sci, Pharmaceuticals, Chem, Life Sci, Medical Imaging or related field & 5 yrs progressive exp w/ pharmaceutical research, In Vivo biomed research & medical imaging OR at least master’s or equiv + 3 yrs exp. Must have 3 yrs exp w/: MRI, bioluminescence, & FLI/FMT, PET, SPECT, CT imaging acquisition & analysis; SARRP radiation admin; & contributing to internal documentation, incl. imaging manuals, SOPs & training mods. Resume & Cover Letter to Irina Bobrovnikov, 10 Moore Dr, Durham, NC 27709. Refer to Job Code VM102021.

Labcorp Drug Development

Research Associate II

Senior Biostatistician Manager Canada Remote Worker The Emmes Company, LLC ("Emmes) is a global, full-service Clinical Research Organization dedicated to excellence in supporting the advancement of public health and biopharmaceutical innovation. We believe in the power of truth, so much so that we named our company Emmes, which means truth. Through decades of experience we have learned that collaborative relationships thrive and human health benefits when truth is our compass. Our "Character Achieves Results" culture is driven by five key values that guide our actions in the way we conduct research and distinguish us as an organization: Integrity, Agility, Passion for Excellence, Collaborative Partnerships and Intellectual Curiosity. We are a trusted partner to clients who share our passion for improving public health in a world of ever-changing scientific research. If you share our motivations and passion in research, come join us! You will be joining a collaborative culture that empowers every Emmes employee — from entry level through top executive — to contribute to our clients' success by sharing ideas openly and honestly. Primary Purpose The Senior Biostatistician Manager oversees statistical activities and deliverables across a broad research area, Provides guidance and oversight to other senior statistical staff and ensures timely and high-quality completion of statistical activities. Responsibilities <ul><li> Manages a team of Biostatistician Managers and is responsible for statistical deliverables across a broad research area </li><li> Serves as a client point of contact for statistical deliverables on large projects, fostering a collaborative relationship with contract sponsors and Emmes project team members </li><li> Manages statistical resources (i.e. budget and personnel) across a broad research area to ensure statistical tasks are completed on schedule and that each project has adequate staffing levels </li><li> Develops strategic vision for the department in collaboration with the Director of Biostatistics </li><li> Across a broad research area at Emmes, serves as the identified internal point of contact for other corporate and senior project staff for management of budgeting, staffing, and statistical activities </li><li> Participates in recruiting activities for new statistical staff members and makes hiring decisions </li><li> Serves as a statistical expert and provides consultation to projects across the company </li><li> Supervises and mentors senior statistical staff, promotes career development and growth for senior staff </li><li> Represents Emmes at Sponsor, Regulatory, Investigator or Safety Review meetings (e.g., Data and Safety Monitoring Board Meetings) </li><li> Establishes budgets for statistical activities on new project work </li><li> Identifies statistical and operational issues and proposes solutions </li><li> Prepares, reviews and/or approves clinical project material that requires statistical input to ensure that the documents are scientifically valid and feasible </li><li> Reviews work processes, schedules and checklists to ensure that all routine activities, as documented in corporate and project-specific Standard Operating Procedures (SOPs), are efficiently performed </li><li> Participates in project and corporate quality assurance activities, particularly those of a statistical nature </li><li> Ensures that project staff is trained and mentored, supervises project staff and performs personnel reviews </li><li> Provides project updates to Director of Biostatistics </li><li> Other duties as assigned </li></ul> Experience <ul><li> MS or PhD in statistics, biostatistics, epidemiology or related field required </li><li> At least 7 (with PhD) or 10 (with MS) years of related experience required; including leading a clinical research team and supervising senior level statistical staff </li><li> Expertise in state-of-the-art data manipulation and statistical analyses </li><li> Proven effective leadership of a clinical research team </li><li> Strong skills in prioritization, problem-solving, organization, decision-making, time management, negotiation, mentoring and planning </li><li> Self-motivated, proactive and detail-oriented </li><li> Demonstrated ability to manage multiple tasks, while working independently </li><li> Ability to effectively communicate technical concepts, both written and oral </li></ul> CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - The Emmes Company, LLC The Emmes Company, LLC is an equal opportunity affirmative action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.

Biostatistician Jobs