Clinical Operations Leader / Clinical Trial Manager team members at Parexel average close to 10 years with the company and we are expanding our team. We currently have Home Based Clinical Operations Leader/Clinical Trial Manager positions available in the US. As the Clinical Liaison to the Project Leader, the COL/CTM leads the clinical aspect of the trial and has a direct

Key Accountabilities Start up (from site identification through pre initiation) Act as Parexel's direct point of contact with assigned sites, accountable for quality and delivery during the start up phase. Build relationships with investigators and site staff. Conduct, drive and manage country specific feasibility and/or site pre qualification and qualification activities

At Parexel you'll team up with some of the best minds in the industry to get new treatments to the patients who need them most. Parexelis one of the largest providers of medical writing services worldwide and has managed thousands of writing projects in more than 29 countries in North and South America, Europe, Asia, and Africa. As a result of continued customer satisfact

Currently hiring a Principal Clinical Regulatory Medical Writer to work r emote from any location in the US. ( Full time) The Principal Medical Writer will research, create, and edit all documents associated with clinical research. The Principal Medical Writer may operate as the project lead writer/submission coordinator and primary client contact to manage contributions

Act as senior therapy area/content expert and lead the delivery of assigned programs/projects within account team, interacting directly with client and KOLs Develop high quality scientific content by means of all necessary research, scientific writing, editing, and fact checking, to meet deadlines while working within project scope and objectives. Applies to all formats o

Do you want to make an impact in your next role? Parexel is looking for changemakers who are driven by curiosity, passion, and optimism. Come join us in keeping the Patient at the Heart of Everything We do. Parexel is seeking an experienced Workday HCM Compensation Implementation Specialist to join our HR Systems team. As an HCM Compensation SME, you will be responsible f

Senior Regulatory Affairs Associate Experience Biologic CMC 5+ years of experience Supported the CMC activities related to Vaccine/Biologic manufacturing and control including authoring of submission dossiers related to new application, post approval variations Understanding of EU/CA/WHO/US regulations & guidance allowing appropriate review and compilation of data to appr

Bring your regulatory expertise and passion for combination products to Parexel! Excellent opportunity for a "cradle to crypt" Medical Device Regulatory professional to share their expertise with multiple clients with innovative technologies! Parexel's incredible Regulatory Consulting team is currently seeking a Combination Product Senior Regulatory Affairs Consultant to

If you are passionate about innovative therapies, love leading complex regulatory filings, and live for quality, on time, and within budget project deliverables, Parexel is E X P A N D I N G and we currently have openings for Senior Regulatory Affairs Consultants / Regulatory Affairs Leads. These are incredible opportunities to join a tight knit team of amazingly nice and

We are looking for a Azure Full Stack Developer for our office in Buenos Aires, Argentina. This position will working on the following activities Using Microsoft Azure data PaaS services, will design, build, modify, and support data pipelines leveraging DataBricks and PowerBI in a medallion architecture setting. If necessary, create prototypes to validate proposed ideas a

Parexel has an exciting home based opportunity for a seasoned professional to fill the role of Partnership Lead, Director. The person selected for this role should have extensive experience within the CRO industry, as well as demonstrated client management skills and a strong understand of both sales and delivery. The Partnership Lead, Director is responsible for developi

Parexel Biotech is dedicated to the biotech industry in supporting our customers with more efficient drug discovery strategies and our regulatory expertise and our support to guide them through an NDA and revenue perspective. We leverage our Subject Matter Experts early in the process to consult with customers to guide them on the right pathway. Our goal is to partner wit

We are looking to fill a position for a Laboratory Based Cleaning Verification / Validation Analyst or Engineer working as a full time employee of Parexel FSP on long term assignment onsite at one of our clients located in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. Responsibilities Executes analytical methods, in

Receiving and documenting samples that are submitted for screening assays Tracking the preparation and analysis of high volume of samples submissions per week using automation techniques and current assay guidelines Setup, troubleshooting, and upkeep of automation equipment used for analysis which includes Tecan liquid handling robots and Agilent UPLC's Preparing samples

The Investigator Meeting Planner is responsible for establishing and maintaining relationships with events management vendors who provide services for global Sponsor events. You will oversee the contracting and execution of all Investigator Meetings, ensuring a positive experience for the sites, Sponsor and internal project team. Work with global suppliers to ensure a hig