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<h3>Job Description</h3>
We are looking for a research scientist to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.
In this role you will need to hold an expert understanding of chemistry- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Research and Development Chemist, Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist.
Benefits:
<ul>
<li>This is a full-time or part-time REMOTE position</li>
<li>You’ll be able to choose which projects you want to work on</li>
<li>You can work on your own schedule</li>
<li>Projects are paid hourly starting at $40+ per hour, with bonuses on high-quality and high-volume work</li>
</ul>
Responsibilities:
<ul>
<li>Give AI chatbots diverse and complex chemistry problems and evaluate their outputs</li>
<li>Evaluate the quality produced by AI models for correctness and performance</li>
</ul>
Qualifications:
<ul>
<li>A current, in progress, or completed Masters and/or PhD is preferred but not required</li>
<li>Fluency in English (native or bilingual level)</li>
<li>Detail-oriented</li>
<li>Proficient in chemistry, inductive/deductive reasoning, physical/temporal/ spatial reasoning</li>
</ul>
Note: Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. This job is only available to those in the US, UK, Canada, Australia, or New Zealand. Those located outside of these countries will not see work or assessments available on our site at this time.

Chemical Engineer

Research Chemist

Chemical Technician

Senior Chemist

Quality Control Chemist

<h3>Job Description</h3>
Job Description
Akkodis is seeking a Research Associate for a Contract job with a client in Waltham, MA. Responsibilities include implementing molecular biology techniques and collaborating on in vitro and in vivo screening studies.
Rate Range: $50/hour to $55/hour; The rate may be negotiable based on experience, education, geographic location, and other factors.
Research Associate job responsibilities include:
<ul>
<li>
Support and execute NGS workflows, including amplicon sequencing and RNA-seq for in vitro and in vivo studies.
</li>
<li>
Operate and maintain sequencing instruments, such as Illumina NextSeq, ensuring high-quality data output.
</li>
<li>
Collaborate with cross-functional teams to process samples and implement molecular biology and biochemistry techniques.
</li>
<li>
Maintain accurate experimental records and perform data analysis using NGS platforms.
</li>
<li>
Present findings in internal meetings and contribute to experimental design and troubleshooting.
</li>
<li>
Manage lab automation tools and ensure adherence to quality control procedures and timelines.
</li>
</ul>
Desired Qualifications:
<ul>
<li>
Bachelor’s or master’s degree in biotechnology, Molecular Biology, or a related field.
</li>
<li>
At least 2 years of hands-on experience with next-generation sequencing techniques.
</li>
<li>
Proficiency in RNA-seq and amplicon sequencing, with experience operating Illumina NextSeq instruments.
</li>
<li>
Familiarity with NGS data analysis platforms and laboratory automation tools for sequencing workflows.
</li>
</ul>
If you are interested in this role, then please click APPLY NOW. For other opportunities available at Akkodis, or any questions, feel free to contact me at Prakhar.Gupta@akkodisgroup.com
 Pay Details: $50.00 to $55.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to <a href="https://www.akkodis.com/en/us/candidate-privacy-policy" target="_blank">https://www.akkodis.com/en/us/candidate-privacy-policy</a> The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: 
<ul>
<li>The California Fair Chance Act</li>
<li>Los Angeles City Fair Chance Ordinance</li>
<li>Los Angeles County Fair Chance Ordinance for Employers</li>
<li>San Francisco Fair Chance Ordinance</li>
</ul>
 Company DescriptionGlobal Footprint, Local Impact: As part of the world's second-largest ER&amp;D company, you'll join a network of 50,000 professionals across 30 countries, each contributing to impactful projects worldwide while benefiting from a close-knit community at a local level. Diverse Career Paths: With services ranging from specialist recruitment to cloud infrastructure and sustainability, Akkodis offers a multitude of career paths. Whether you're a software developer, data analyst, or sustainability expert, there's a place for your skill set. Commitment to Innovation: Innovation is our cornerstone. With continuous investments in analytics and market intelligence, we not only predict the future of technology – we create it. Your ideas and innovations will have the space to flourish. Continuous Learning and Development: The Akkodis Academy offers unrivaled opportunities for learning and professional growth, ensuring you remain at the forefront of your field. Our culture values continuous improvement, both for our company and for your career. Inclusive and Collaborative Culture: We believe in the power of diverse perspectives and collaborative work environments. At Akkodis, you'll find a community where inclusivity drives innovation and where every voice is heard. Our Evolution and Your Role in It Akkodis emerged from the strategic merger of AKKA Technologies and Modis in 2023, under the Adecco Group. This fusion created a powerhouse in digital engineering and technology, blending European engineering finesse with global technological capabilities. As we write our next chapter, your skills and vision will be instrumental in driving our continued success. Empowering the Future We're not just creating solutions; we're empowering industries to be more efficient, sustainable, and forward-thinking. Our work in industrial automation, product development, and custom software solutions is setting new standards in technology and engineering. Join the Akkodis Community At Akkodis, you're more than just an employee – you're a vital part of a community shaping the future. We're excited to see where your expertise can take us. Discover where you fit in our diverse range of opportunities and start engineering a smarter future with us today. 
<h3>Company Description</h3>
Global Footprint, Local Impact: As part of the world's second-largest ER&amp;D company, you'll join a network of 50,000 professionals across 30 countries, each contributing to impactful projects worldwide while benefiting from a close-knit community at a local level.\r\n\r\nDiverse Career Paths: With services ranging from specialist recruitment to cloud infrastructure and sustainability, Akkodis offers a multitude of career paths. Whether you're a software developer, data analyst, or sustainability expert, there's a place for your skill set.\r\n\r\nCommitment to Innovation: Innovation is our cornerstone. With continuous investments in analytics and market intelligence, we not only predict the future of technology – we create it. Your ideas and innovations will have the space to flourish.\r\n\r\nContinuous Learning and Development: The Akkodis Academy offers unrivaled opportunities for learning and professional growth, ensuring you remain at the forefront of your field. Our culture values continuous improvement, both for our company and for your career.\r\n\r\nInclusive and Collaborative Culture: We believe in the power of diverse perspectives and collaborative work environments. At Akkodis, you'll find a community where inclusivity drives innovation and where every voice is heard.\r\n\r\nOur Evolution and Your Role in It\r\n\r\nAkkodis emerged from the strategic merger of AKKA Technologies and Modis in 2023, under the Adecco Group. This fusion created a powerhouse in digital engineering and technology, blending European engineering finesse with global technological capabilities. As we write our next chapter, your skills and vision will be instrumental in driving our continued success.\r\n\r\nEmpowering the Future\r\n\r\nWe're not just creating solutions; we're empowering industries to be more efficient, sustainable, and forward-thinking. Our work in industrial automation, product development, and custom software solutions is setting new standards in technology and engineering.\r\n\r\nJoin the Akkodis Community\r\n\r\nAt Akkodis, you're more than just an employee – you're a vital part of a community shaping the future. We're excited to see where your expertise can take us. Discover where you fit in our diverse range of opportunities and start engineering a smarter future with us today.

Research Associate

<h3>Job Description</h3>
Job Description
This is a full-time 40 hour a week position. (Schedule is 4 days, 10 hour shifts) 
THE POSITION:
The Senior Microbiology Medical Technologist (MT) works in collaboration with the veterinary staff and the Pathology team to provide Angell clientele with high quality clinical and anatomical laboratory services. The Senior Microbiology MT will assist in the opening of the new, state of the art Microbiology laboratory. The Senior Microbiology MT will help set up the laboratory space and workflow, train on all new Microbiology analyzers, train laboratory employees on microbiology procedures, develop and modify existing and new procedures and protocols, establish and monitor QC programs and help oversee the microbiology laboratory when required by Management. The Senior Microbiology MT uses a variety of technical and analytical skills to perform and evaluate various laboratory test procedures to aid the doctors in the diagnosis, treatment and monitoring of patients to provide accurate and timely results. The Senior Microbiology MT will be cross trained into the Clinical Pathology laboratory as a generalist after becoming proficient in the microbiology laboratory. This position also requires collaboration and daily interaction with the clinical pathology laboratory. Working knowledge of current Microbiology practices, use of Maldi-Tof technology and the most updated CLSI and ASM guidelines is a preferred. Experience reading and evaluating all microbiology benches both human and veterinary is optimal.
Some of the duties include:
<ul>
<li>
<ul>
<li>Possesses and demonstrates technical and theoretical knowledge of clinical and veterinary Microbiology.</li>
<li>Responsible for reading all microbiology culture plates and processing all appropriate testing for those cultures.</li>
<li>Responsible for the training of new and current employees in the microbiology laboratory. Updates training protocols and procedures as needed. Accurately records, discusses and troubleshoots trainee’s progress with the supervisor and lab management. Provides timely feedback for all trainees to lab management as needed.</li>
<li>Performs clinical testing and complex analysis of biological materials. Testing includes analysis of not only patient specimens but also proficiency samples, quality control (QC) material and calibration of methods, equipment and instruments.</li>
<li>Evaluates patient test results to verify validity of results and identify and resolve any inconsistencies in patient results. Provides clinical expertise to the patient care staff with the interpretation of results and/or complex laboratory problems.</li>
<li>Operates, maintains, troubleshoots and resolves issues with laboratory instrumentation, equipment and test assays. Documents minor repairs and maintenance procedures. Consistently uses available resources to maintain and repair instruments or problem solves assay issues.</li>
</ul>
</li>
</ul>
WHO WE ARE:
The Boston MSPCA-Angell is one of the oldest and most venerable humane organizations in the world, and working in an environment that clearly delivers on its mission of advancing the health and welfare of animals adds an important dimension to our work.
APPLICANT REQUIREMENTS: 
Education: Graduate of NAACLs accredited Clinical Laboratory Science program with certification as a Medical Technologist (MT), Medical Laboratory Scientist (MLS), Clinical Laboratory Scientist (CLS) or Microbiology Specialist (M ASCP) by ASCP or other nationally recognized credentialing agency is required. Bachelor of Science in a medical discipline with 5+ years of veterinary or human microbiology bench reading experience will be considered.
Experience: 5+ years of current Microbiology bench reading experience is preferred. Both veterinary and human microbiology experience will be considered.
OUR BENEFITS:
Our compensation package includes health, dental and life insurance, 403(b) retirement plan, tuition reimbursement, paid holidays, sick, and vacation time, employee discounts for pet health care, and free on-site parking.
If you are interested in working for an organization where your work is an important part of a respected and caring non-profit, this may be the career change you are looking for.

Senior Microbiology Medical Technologist

<h3>Job Description</h3>
Job title: Global Scientific Communications Lead – Rare Disease
Location: Cambridge, MA
About the job
We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&amp;D to sales, our talented teams work together, revolutionizing treatment, continually improving products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.​
Associate Director, Global Rare Diseases Scientific Communications &amp; Publications, oversees the development and execution of the strategic publication and scientific communication plan for multiple indications including launched products and development indications in the Rare Franchise.
We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&amp;D to sales, our talented teams work together, revolutionizing treatment, continually improving products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.
Main Responsibilities:
The Scientific Communications Lead will closely collaborate with external thought leaders and internal stakeholders in the medical, scientific affairs, biostats and clinical development teams by leading:
<ul>
<li>
Strategic publication planning and execution: Overseeing the development of abstracts for medical and scientific congresses, posters, platform presentations, manuscripts, and journal publication enhancements.
</li>
<li>
Scientific communications strategic planning and resource development: Creating scientific platforms, lexicons, FAQs, and backgrounders, as well as supporting content development for advisory boards.
</li>
<li>
Medical education planning and execution: Developing content for live education programs, congress symposia, online and multichannel HCP education, field medical tools, slide decks, medical booth resources, and omnichannel engagement assets.
</li>
<li>
This role reports to the Director Global Scientific Communications for launch indications within Rare Diseases in Global Medical Affairs at Sanofi.
</li>
<li>
Collaboration with external authors and academic experts is essential to drive execution of high quality and relevant publications and medical education materials to address educational and data gaps and inform strategic decision making.
</li>
<li>
In addition to investigators/authors, a key element of this role involves managing scientific agencies and requires working closely with cross-functional teams and internal stakeholders, particularly from the Registry, Research and Clinical Development, to drive the data generation strategy and integration of scientific, clinical, and business priorities.
</li>
<li>
The Scientific Communications Lead will have experience and a proven track record of success in the biotechnology or pharmaceutical industry, with a strong background in scientific research, publication planning, medical communications, and medical affairs activities
</li>
</ul>
About You
Qualifications and Skills:
<ul>
<li>
Advance degree in life sciences or pharmaceutical sciences (PhD, PharmD, MD or MS) with 2+ years of relevant medical affairs experience.
</li>
<li>
A minimum of 2+ years pharma/biotech industry in a global role
</li>
<li>
Experience working in a matrix organization and across team is preferred.
</li>
<li>
Ability to interpret and critique scientific and medical data with respect to scientific and business implications are essential.
</li>
<li>
Experience and demonstrated skill in the analysis, communication, and presentation of complex scientific and medical data.
</li>
<li>
Track record of successfully developing peer-reviewed publications is required.
</li>
<li>
Exemplary customer facing skills, and ability to collaborate with external Key Opinion Leaders on data dissemination strategies in a credible, responsive and customer focused manner is a necessity.
</li>
<li>
Excellent interpersonal and communication skills, written and verbal; comfortable and experienced in making presentations.
</li>
<li>
Demonstrated ability to work effectively in a matrix environment.
</li>
<li>
Experience collaborating with and supporting international medical scientific teams.
</li>
<li>
Knowledge of industry guidelines pertaining to data dissemination (e.g., CONSORT, ICMJE, GPPs) and interactions with health care providers (e.g., PhRMA Code, AdvaMed guidelines)
</li>
</ul>
Why Choose Us?
<ul>
<li>
Bring the miracles of science to life alongside a supportive, future-focused team.
</li>
<li>
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
</li>
<li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
</li>
<li>
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
</li>
</ul>
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law
#GD-SG &nbsp;​ &nbsp;#LI-GZ
#LI-Onsite
#vhd
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

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