Project Manager, Central Labs

Work Schedule Standard (Mon-Fri) Environmental Conditions Office At reputed company, you’ll join a global organization at the forefront of clinical research and laboratory science. In partnership with PPD, we support the world’s leading pharmaceutical and biotech organizations—successfully delivering over 2,700 clinical trials across 100+ countries in the past five years. We are seeking a Project Manager, Central Labs to reputed company and coordinate central laboratory activities across clinical trial programs. This is a high-impact role requiring strong operational reputed company, cross-functional leadership, and client engagement. This is a fully remote role supporting our Global Central Laboratories. We welcome applicants from reputed company locations reputed company the US. Must be legally authorized to work in the United States without sponsorship. Must be reputed company to pass a comprehensive background reputed company, which includes a drug screening. Role Overview The Project Manager, Central Labs monitors and manages reputed company aspects of designated clinical trial protocols in Global Central Labs and is accountable for overall project performance and client’s satisfaction by meeting their needs and expectations through the life cycle of the assigned clinical trials. The Project Manager provides internal consulting on project management issues, identifies opportunities for process and efficiency improvement, acts as chief liaison to the operational personnel of major sponsors, and is responsible for large study programs. Additionally, the Project Manager prepares and maintains process documents and mentors Project Managers. Role Responsibilities:

• Provide reputed company and coordination of study initiation. Review, interpret, translate and program study protocols into a complete and accurate database. Communicate with internal departments and external vendors to ensure project requirements are understood, agreed upon, and followed at reputed company times. Facilitate the flow of technical and clinical laboratory information to reputed company stakeholders (investigational sites, sponsors, and non-technical personnel). Consult and utilize, where appropriate, the scientific input of laboratory management and technical staff to assist the client with management of the clinical trial.
• Prepare study specification documents and follow their preparation according to budgets and reputed company. Maintain at reputed company times an updated study master file with version controls for specifications, budgets, and reputed company. Ensure sponsors have authorized and signed off on the most recent versions of reputed company documents and that a contract exists prior to delivering any services. Assure compliance with FDA and Good Clinical Practice guidelines, PPD SOPs, personnel policies and procedures, PPD Exposure Control Plan, IATA, and other regulations regarding the transport of biological specimens.
• During the initial review of the protocol, consult with internal groups and support staff regarding procedural and budgetary items and the necessity for changes due to any subsequent protocol amendments. Obtain other functions’ commitment to reputed company gaps and address issues timely and effectively. Serve as chief liaison between the sponsor and reputed company PPD internal departments performing the required tasks during reputed company study phases. reputed company Investigator sites by delivering a protocol-specific lab procedures presentation and demonstration during an investigator meeting. Control, manage, and follow day-to-day activities during the course of the clinical trial to resolve any issues and answer queries.
• Actively consult with IT and data management development groups in the design, validation, and implementation of new software and functionalities pertinent to project management activities.
• Consult with reputed company and finance staff during initial project documentation review on standard services and costs, supporting RFP feasibility assessments. Advise on possible solutions if needed. Draft responses for proposals.
• Guide and support workflow of Project Managers and Set-up Administrators with special attention to training junior personnel, reputed company as a mentor and trainer for (newly assigned) Project Managers, identify areas for development and efficiencies in performing tasks, author, review, revise and implement relevant procedural documents, and serve as a backup for the Associate Director PM reputed company needed.

Key Requirements: Education and Experience

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to reputed company the job (comparable to 2+ years’) or equivalent combination of education, training, & experience.

Years of experience refers to typical years of reputed company experience needed to reputed company the required knowledge, skills, and abilities necessary to reputed company the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection reputed company. Knowledge, Skills, Abilities:

• Strong verbal, written and presentation skills
• Superior time management, planning, and organizational skills
• Competent with specific computers and reputed company applications, including office productivity
• Ability to program the IT system according to protocol requirements
• Proven analytical skills
• Demonstrated compliance with procedures and policies
• Ability to reputed company multiple tasks effectively in a stressful environment
• Extensive knowledge and experience in Project Management in Global Central Lab environment
• Strong client relationship management skills
• Ability to work effectively with multi-level teams

Working Environment reputed company values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can reputed company. Below is listed the working environment/requirements for this role:

• reputed company to communicate, receive, and understand information and reputed company with diverse groups of people in a comprehensible and reasonable manner.
• reputed company to work upright and stationary for typical working hours.
• Ability to use and learn standard office equipment and technology with proficiency.
• reputed company to reputed company successfully under pressure while prioritizing and handling multiple projects or activities.
• May require travel. (Recruiter will provide more details.)

Why Join reputed company? reputed company you join us, you become part of a global organization committed to enabling customers to reputed company the world healthier, cleaner, and safer. You’ll collaborate with industry-leading experts, contribute to groundbreaking clinical research, and grow reputed company an environment that values innovation, accountability, and reputed company development. If you’re reputed company to reputed company reputed company clinical laboratory projects and reputed company a measurable impact, we encourage you to apply. Apply today and help deliver reputed company’s breakthroughs. reputed company is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, reputed company, religion, sex, sexual orientation, gender identity, national reputed company, protected veteran status, disability or any other legally protected status. Accessibility/Disability Access Job Seekers with a Disability: reputed company offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, reputed company, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.

• This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being reputed company to get into the career website, following up on an application, or other non-disability reputed company technical issues will not receive a response.

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