Work Schedule

Environmental Conditions

Job Description

This is a fully onsite role based at our BioAnalytical in Richmond, VA. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.  

Must be legally authorized to work in the United States without sponsorship. 

Must be able to pass a comprehensive background check, which includes a drug screening. 

The working schedule for this role is 1st shift - Monday - Friday from 8AM-5PM.

Join Us as an Associate Research Scientist – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotech companies, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As an Associate Research Scientist, you will oversee complex laboratory analysis of pharmaceutical products, calculate and analyze data and record data in adherence with PPD SOP's and the industry. You will routinely act as the project leader on multiple projects, interact with clients, review and evaluate data, write reports and protocols. You will be responsible for the scientific conduct of the project and communication of regulatory issues with senior level team members.

What You'll Do:
•Understands and conforms to methods and protocols applicable to assigned tasks. Designs and drives experiments with minimal supervision.
•Prepares study protocols, project status reports, final study reports and other project-related technical documents.
•Communicates data and technical issues to the client and responds to client needs and questions.
•Mentors, trains and coordinates laboratory activities of other team members and assists in troubleshooting instrument and analytical problems.
•Assists with quality systems and new equipment.
•Assists in establishing project timelines.
•Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP). Performs peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.

Knowledge, Skills, Abilities:
•Full understanding of laboratory requirements, PPD & client SOPs, ICH guidelines, USP requirements and FDA guidance
•Ability to apply Microsoft Excel and Word to perform tasks
•Proficiency on technical operating systems
•Proven problem solving and troubleshooting abilities
•Effective oral and written communication skills
•Proven ability in technical writing skills
•Time management and project management skills
•Ability to work in a collaborative work environment with a team
•Proven problem solving and troubleshooting abilities
•Ability to train junior staff

Education

• Bachelor's degree in lab sciences such as biology, biochemistry, immunology, chemistry, molecular biology or similar Experience

• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable 6+ year) or equivalent combination of education, training, & experience.

• OR Masters degree and previous experience that provides the knowledge, skills, and abilities to perform the job (comparable 4+ year)

• OR PhD (preferred) and previous experience that provides the knowledge, skills, and abilities to perform the job (comparable 2+ year)

• In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Work Environment:
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
•Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
•Able to work upright and stationary and/or standing for typical working hours.
•Able to lift and move objects up to 25 pounds.
•Able to work in non-traditional work environments.
•Able to use and learn standard office equipment and technology with proficiency.
•May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
•Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.

Compensation and Benefits

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

• A choice of national medical and dental plans, and a national vision plan, including health incentive programs

• Employee assistance and family support programs, including commuter benefits and tuition reimbursement

• At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

• Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

• Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards