When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
We are looking to fill a Bioanalytical Scientist position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in Springhouse, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship.
Responsibilities
Develop and qualify ligand-binding or cell-based based bioanalytical assays to support high priority biological and vaccine programs.
Analyze clinical samples using multiple platforms such as MSD, Luminex, or neutralization assays
Assess analytical result data on acceptability using LIMS or other computer software
Work according to established Standard Operating Procedures (SOPs) and regulatory guidance
Maintain accurate records of ongoing projects in adherence with ALCOA+ principles
Assist in generation and review of regulated documents and contribute to assay trouble shooting efforts
Collaborate and communicate within and across the work group
Work in a structured environment under direct to moderate supervision
Adhere to GxP regulations and safety requirements in BSL-2
Qualifications :
Degree in Molecular Biology, Immunology, Cell Biology, Biology, Biochemistry, Biology, or related biological science discipline
Scientist 2: B.S./B.A. 1-2 years of experience
Scientist 3: B.S./B.A. 3-5 years of experience or MS 1-2 years of experience
Required Skills and Experience
Experience with immunogenicity assays such as ELISA, Luminex, or MSD
Well versed in serology with excellent pipetting skills
Working experience in a regulated environment (GxP, preferably GLP or GCLP)
Strong experience with Laboratory Information Management System (LIMS)
Strong computer, scientific, and organizational skills
Excellent communication (oral and written) and attention to detail
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Desired Skills and Experience
Experience in cell culture and cell-based assays
Experience with Benchling LIMS
Ability to manage multiple projects under tight timeline and problem-solving skills
High sense of responsibility, accountability, and professional integrity
Experience with liquid handlers such as Biomek or end-to-end robotic platforms using Momentum
About Parexel
Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies.
For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement.
Come join us!
#LI-DK1
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.
Community Guidelines
Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are:
• Abusive, harassing or threatening to others.
• Defamatory, offensive, obscene, vulgar or depicting violence.
• Hateful targeting by race/ethnicity, age, color, creed, religion, gender,
sexual preference or orientation, nationality or political beliefs.
• Sexually explicit or pornographic.
• Fraudulent, deceptive, libelous, misleading or unlawful.
• Referencing criminal or illegal activity.
• Spamming.
We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.
