9,797 Senior Research Associate jobs in the United States

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
**Job Description**
At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
We empower our leaders to step up, share ideas, listen, learn, and lead. We're welcoming bright, diverse, and imaginative minds; we're nurturing them to foster an environment of inclusion and growth where innovation is encouraged. We expect our people leaders to model that environment, and to focus on creating inclusion, developing talent, and enabling teams.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact. Join Gilead and help create possible, together.
**Job Description**
Research Associate in the Biologics Pivotal & Commercial Cell Culture Process Development function will execute cell culture process development laboratory experiments for Gilead biologics entities during pivotal development (phases II/III, commercial). They will also support cell culture process technology development, platform process initiatives, and implementation of cell culture processes in pilot plant and GMP facilities.
**At a future date this position will relocate to the corporate HQ in Foster City, CA**
**Key Responsibilities:**
+ Plan and execute experiments to support cell culture process optimization and characterization during pivotal development phases.
+ Support cell culture platform development and pilot plant operations, as needed.
+ Maintain a state-of-the-art cell culture process development laboratory, including equipment upkeep and consumables management.
+ Participates in the equipment maintenance and continued improvement of lab and data handling best practices.
+ Ensure high-quality and timely documentation of data in electronic laboratory notebooks.
+ Collect, analyze, and visualize data from laboratory experiments.
+ Present results of work, interprets data, and draws conclusions regarding presented material and nature of work.
+ Author experimental protocols and reports.
+ Travel as required to support technology transfers and provide oversight at both internal and external manufacturing facilities.
+ Adhere to department budget and all trainings, regulatory compliance, and safety requirements.
**Basic Qualifications:**
+ Bachelor's OR
+ Associate and 2+ years of relevant experience OR
+ High School Diploma/GED and 3+ years of relevant experience
**Preferred Qualifications:**
+ A relevant scientific discipline (e.g., bioengineering, chemical engineering, biochemical engineering).
+ Hands-on laboratory operations experience including shake flasks, high-throughput bioreactors, bench scale bioreactors, and pilot scale bioreactors.
+ Experience in pivotal stage cell culture process development and implementation in GMP facilities is a plus.
+ Excellent communication, technical writing, presentation skills and aptitude for creative problem solving.
+ Demonstrated ability to collaborate, work in a team setting, and influence cross-functionally.
The salary range for this position is: $74,715.00 - $96,690.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.
For additional benefits information, visit:
Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
**For jobs in the United States:**
Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact for assistance.
For more information about equal employment opportunity protections, please view the 'Know Your Rights' ( poster.
NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT ( RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT
PAY TRANSPARENCY NONDISCRIMINATION PROVISION ( environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.
Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.
**For Current Gilead Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.

**Research Associate - Cell Therapy Process Development**
**Location:** Winston-Salem, NC (Onsite 5 Days/Week)
**Schedule:** Monday-Friday, 9:00 AM-5:00 PM
**Salary:** $70,000 annually
*This role does not offer relocation assistance or visa sponsorship.
**Position Summary:**
An innovative biotechnology company is seeking a **Research Associate - Cell Therapy Process Development** to support lab-based efforts to develop and optimize cutting-edge cell therapy manufacturing processes. This is a fully onsite role, ideal for candidates with a strong scientific background in biology or related fields, and hands-on experience with cell culture techniques in an academic or industry setting. The individual in this position will contribute to key R&D activities, support technology transfer efforts, and receive structured training while working closely with cross-functional teams.
**Key Responsibilities:**
+ Execute laboratory experiments to support the development and optimization of manufacturing processes for cell-based therapies, including media prep, cell expansion, harvesting, and formulation.
+ Perform hands-on cell culture work in a cleanroom or lab environment, following strict aseptic techniques.
+ Analyze experimental data and communicate results clearly to internal teams; participate in regular project meetings and updates.
+ Assist in troubleshooting experiments and improving existing protocols in collaboration with team members.
+ Support process validation and technology transfer activities as new methods and systems move toward GMP clinical and commercial use.
+ Draft and revise technical documents including batch records, SOPs, protocols, and reports.
+ Participate in maintaining documentation in accordance with GMP and regulatory standards.
+ Collaborate with Quality Assurance, Manufacturing, and Regulatory teams to ensure compliance and effective process development support.
+ Maintain lab equipment and materials, and follow safety protocols consistently.
+ Work onsite in the lab five days a week; occasional weekend work may be required depending on project timelines.
**Qualifications:**
+ Bachelor's or Master's degree in Cell Biology, Biotechnology, Biochemical Engineering, or a related scientific field.
+ 1-3 years of hands-on experience in a research, academic, or industry lab environment-cell culture experience required.
+ Experience working with cell therapy products is a plus, but not required.
+ Comfortable working in a fast-paced, fully onsite laboratory setting.
+ Strong scientific foundation and an eagerness to continue learning and developing new technical skills.
+ Excellent written and verbal communication skills; ability to document results and follow protocols accurately.
+ Basic understanding of GMP, GLP, or other regulatory frameworks is a plus.
+ Proficiency with Microsoft Office; experience using electronic lab notebooks or data analysis software (e.g., JMP) is helpful.
+ Must be comfortable handling human tissue samples and following safety protocols.
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly ® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.
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Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

Our client, a organization in the scientific research industry, is seeking a Research Associate Scientific III to join their team. As a Research Associate Scientific III, you will be part of the analytical chemistry department supporting critical research initiatives. The ideal candidate will have strong analytical problem-solving skills, excellent communication abilities, and a collaborative spirit which will align successfully in the organization.
**Job Title:** Research Associate Scientific III
**Location:** Round Lake, IL (Onsite)
**What's the Job?**
+ Conduct nitrosamines and impurities evaluations through chemical analysis utilizing LC/MS/MS and associated wet chemistry techniques.
+ Perform solid-phase extraction (SPE) and liquid-liquid extraction (LLE) in support of nitrosamines studies.
+ Independently plan and execute method development activities utilizing LC/MS/MS.
+ Document and review laboratory work using an electronic laboratory notebook following good documentation practices.
+ Communicate project status and hurdles clearly with management and cross-functional teams.
**What's Needed?**
+ Extensive hands-on experience with mass spectrometry analysis, specifically MS/MS via HPLC or UHPLC.
+ Demonstrated knowledge of analytical chemistry with relevant laboratory skills.
+ Strong written and verbal communication skills in English.
+ Ability to objectively assess, organize, and communicate information effectively.
+ Proficiency in Microsoft Office applications (Excel, Word, Outlook).
**What's in it for me?**
+ Opportunity to work in a dynamic and innovative research environment.
+ Engagement in meaningful projects that contribute to scientific advancements.
+ Collaboration with experienced subject matter experts in the field.
+ Professional growth and development opportunities.
+ Access to a supportive and inclusive workplace culture.
**Upon completion of waiting period consultants are eligible for:**
+ Medical and Prescription Drug Plans
+ Dental Plan
+ Vision Plan
+ Health Savings Account
+ Health Flexible Spending Account
+ Dependent Care Flexible Spending Account
+ Supplemental Life Insurance
+ Short Term and Long Term Disability Insurance
+ Business Travel Insurance
+ 401(k), Plus Match
+ Weekly Pay
If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!
**About ManpowerGroup, Parent Company of: Manpower, Experis, Talent Solutions, and Jefferson Wells**
_ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands -_ **_Manpower, Experis, Talent Solutions, and Jefferson Wells_** _-_ creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent.
ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
**Job Description**
**Key Responsibilities:**
+ Plan and execute experiments to support cell culture process development.
+ Establish and maintain a state-of-the-art cell culture process development laboratory.
+ Execute studies for cell culture process technology development and platform process evolution projects for increased productivity, high quality product, and speed to clinic.
+ Contribute to design of and conduct laboratory scale experiments; hands-on laboratory execution is expected, including weekends.
+ Maintain cell culture laboratory equipment and supplies.
+ Author experimental protocols and reports.
+ Ensure high-quality, timely documentation in electronic laboratory notebooks and reports.
+ Collect and analyze data from laboratory experiments.
+ Travel as required to support technology transfers and provide oversight at external manufacturing facilities.
+ Support cell culture platform development and pilot plant operations as needed.
+ Adhere to department budget and all training, compliance and safety requirements.
**Basic Qualifications:**
**Bachelor's Degree and Two Years' Experience**
**OR**
**Masters' Degree**
**Preferred Qualifications/Skills/Experience:**
+ M.S. **OR** B.S. with 2+ years in a relevant scientific discipline (biology, bioengineering, chemical engineering, biochemical engineering).
+ Hands-on laboratory operations experience including shake flask, high-throughput bioreactor, bench scale bioreactor, and pilot scale cultures.
+ Experience in pre-pivotal stage cell culture process development and implementation in GMP facilities.
+ Excellent communication, technical writing, and presentation skills and aptitude for creative problem solving.
+ Working knowledge of lab automation, data management, data science, knowledge management and data protection.
+ Demonstrated ability to creatively solve problems and adapt to changes
+ Demonstrated ability to collaborate, work in a team setting, and influence cross-functionally.
+ Passion for inclusion: knowing the business value of diverse teams, modelling inclusion, and embedding the value of diversity in the way he/she works. 
**People Leader Accountabilities**
+ Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams.
+ Develop Talent - understand the skills, experience, aspirations, and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop, and realize their purpose.
+ Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.
The salary range for this position is: $94,945.00 - $122,870.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.
For additional benefits information, visit:
Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
**For jobs in the United States:**
Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact for assistance.
For more information about equal employment opportunity protections, please view the 'Know Your Rights' ( poster.
NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT ( RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT
PAY TRANSPARENCY NONDISCRIMINATION PROVISION ( environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.
Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.
**For Current Gilead Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.

Our client, a leading pharmaceutical company dedicated to advancing healthcare through innovative drug development, is seeking a highly competent Clinical Research Associate (CRA) to join their esteemed team in Cincinnati, Ohio . This pivotal role will involve managing and overseeing clinical trial sites, ensuring compliance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and study protocols. You will be responsible for site selection, initiation, monitoring, and close-out visits, as well as ensuring the quality and integrity of data collected. The CRA will serve as the primary liaison between the sponsor and clinical trial sites, building strong relationships with investigators and site staff. Key duties include reviewing essential documents, verifying patient safety, and ensuring adherence to protocol. You will also track study progress, manage study supplies, and report on site performance. A thorough understanding of the drug development process and clinical trial phases is crucial. The ideal candidate will possess excellent organizational skills, meticulous attention to detail, and strong communication and interpersonal abilities. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is highly desirable. This is an exciting opportunity to contribute to life-saving research and development in a dynamic pharmaceutical environment.
Responsibilities:

• Conduct site qualification, initiation, interim monitoring, and close-out visits.
• Ensure compliance with study protocols, GCP, and regulatory requirements.
• Verify the accuracy, completeness, and integrity of clinical data.
• Serve as the primary point of contact between the sponsor and study sites.
• Monitor subject safety and report adverse events.
• Manage study supplies and investigational product accountability.
• Facilitate communication and problem-solving at study sites.
• Ensure timely submission of essential documents.
• Train site staff on study-specific procedures.
• Prepare site monitoring reports.

Qualifications:

• Bachelor's degree in a life science, nursing, or related field.
• Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial management role.
• In-depth knowledge of GCP, FDA regulations, and clinical trial processes.
• Experience with EDC systems and CTMS.
• Strong understanding of medical terminology and research methodologies.
• Excellent written and verbal communication skills.
• Highly organized with strong attention to detail.
• Ability to travel to clinical trial sites as required.

Our client, a renowned pharmaceutical company, is actively recruiting a Clinical Research Associate (CRA) to support their groundbreaking drug development programs. This crucial role, based in **Orlando, Florida, US**, involves overseeing and managing clinical trials to ensure compliance with protocols, regulatory requirements, and ethical standards. You will be responsible for site selection and initiation, monitoring patient data, ensuring data integrity, and managing trial documentation. Key responsibilities include conducting pre-study, interim, and close-out visits for clinical trial sites, identifying and resolving study-related issues, and serving as the primary liaison between the sponsor and the investigative sites. The ideal candidate possesses a strong understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements governing clinical trials. Excellent organizational, communication, and interpersonal skills are essential, along with meticulous attention to detail. You must be adept at problem-solving and capable of working independently while managing multiple priorities. We are seeking dedicated professionals committed to advancing patient health through rigorous clinical research. This position offers the opportunity to work on innovative therapies and contribute to bringing life-saving medications to market. You will collaborate closely with investigators, site staff, and internal project teams. A Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field, and a minimum of 3 years of experience as a CRA or in a similar clinical research role are required. Experience with various therapeutic areas is beneficial. Strong knowledge of clinical trial management software and electronic data capture (EDC) systems is essential.

Our client, a world leader in diagnostics and life sciences, is looking for a "Cell Line Development Research Associate ” based out of South San Francisco, CA.

Job Duration: Long term Contract (Possibility Of Further Extension)

Pay Rate: $42/hr on W2

Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K

Cell Line Development Research Associate is involved in the creation of stable cell lines for the recombinant adeno-associated viral vector (rAAV) production processes . He/she executes experiments, produces relevant documentation, and works under supervision. 

Responsibilities:

Culturing mammalian cells for viral production in shake flasks, spinner flasks, spin tubes, deep well and automation platforms.Performing experiments in the development, optimization and scale-up of AAV producer cell lines.Preparing process development protocols, data analysis summaries, technical reports, and other relevant process documentation.Optimization of transfection and transduction protocols for newly engineered cell lines.Maintaining an accurate laboratory notebook.Ensuring work conforms to applicable quality and safety standards.

Qualifications:

B.S. with 3-6 years of experience, MSc with 2-5 years of relevant scientific or technical experience in the life sciences industry or equivalentExperience in cell culture including materials, instruments and technologies is essential.Experience with viral vector production is preferred.Hands-on experience in mammalian cell culture production processes is a critical requirement. This includes small scale (shaker flasks, spinner flasks, spin tubes, deep well) and/or bench top bioreactor scale.Experience with creation, analysis and characterization of new engineered cell lines and stability studies (sub cloning, clonal expansion, transient transfection and expression screening) is a strong plus.Experience in molecular biology techniques (plasmid design, molecular cloning, SDSPAGE/western blotting, qPCR, etc) is a strong plus.Automation and ELN experience is a strong plus.Experience in laboratory automation hardware and software is a plus.Due to the inherent nature of cell culture, some weekend work and/or work on holidays may be needed. On occasion, long work hours may be required depending upon the experiment schedule.Handling large volumes of cell culture or related materials, such as tens of liters, may be required. Also, several viral materials, including AAV may be involved in the work.

If interested, please send us your updated resume at

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Job Title: Research Associate
Location: Rockville, MD
Type: Contract
Hours: Monday-Friday 9AM-5PM
Overview:
Biopharmaceutical Company is looking for a Research Associate for their Rockville, MD site!
Responsibilities:
+ Assay and Data Management: Perform various assays, tests, and studies related to animal modeling. Calculate and analyze raw data to complete research test results. Collate data, perform statistical analyses using software tools such as Microsoft Office, GraphPad Prism, and R Studio. Maintain detailed notes and log data in computer databases and laboratory notebooks.
+ Mammalian Cell Culture: Oversee all aspects of mammalian cell culture, including media and buffer preparation, culture initiation, propagation, and cryopreservation. Handle primary human cells from commercial and patient sources. Ensure that all cell culture procedures are conducted according to standard operating procedures.
+ Flow Cytometry: Assess target antigen expression using traditional and spectral flow cytometry techniques on various in-vitro and ex-vivo samples. Prepare and process samples for cytometric analysis.
+ Dosing Formulations and Reporting: Prepare dosing formulations for in-vivo studies. Report experimental results to the supervisor and collaborate with investigators. Ensure timely and accurate documentation of experimental protocols and data.
+ Record Keeping and Compliance: Maintain detailed and accurate records of experimental data and procedures in laboratory notebooks. Adhere to standard operating procedures and ensure compliance with all regulatory requirements.
Requirements:
- Bachelor's Degree in Animal Science, Biology, or related science field.
- Strong computer skills, including proficiency with basic data analysis programs (Microsoft Office, GraphPad Prism, Pristima, etc.) and programming and data analysis (R Studio, Linux, etc.).
- 2+ years of tissue culture
- 2+ years of traditional and spectral flow cytometry.
System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
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Ref: #558-Scientific
System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.