Study Manager Salary at Kerlo Research Inc BETA

Title: Biomarker Operations Manager or (Sr) Organization: Biomarker & Diagnostic Operations, Oncology Diagnostics Position Description: Kelly FSP is seeking a highly motivated individual to join the Biomarker & Diagnostic Operations team with our pharmaceutical client. As a key contributor to the clinical biomarker and diagnostic strategy, he/she will be accountable for implementation and execution of clinical sample collection, testing and data delivery activities for both early and later phase clinical programs in oncology. The successful candidate will have experience bridging both science and operations though cross functional partnerships, strategic project planning and facilitating key biomarker and diagnostic execution discussions. Key Responsibilities: Drives the implementation and execution of the clinical biomarker and diagnostic strategy for clinical programs in early and late-stage oncology Creates and manages biomarker and diagnostic plan, timelines, budget, risk assessmen

Kelly Science and Clinical FSP is currently seeking a Biomarker Operations Manager for a long-term engagement with one of our Global Pharmaceutical/Medical Device clients. The candidate will need to be near Spring House, PA and be able to go into the office possibly 1 day a week. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time. Title: Biomarker Operations Manager or (Sr) Organization: Biomarker & Diagnostic Operations, Oncology Diagnostics Position Description: Janssen is seeking a highly motivated individual to join the Biomarker & Diagnostic Operations team. As a key contributor to the clinical biomarker and d

KMK is a global data analytics and technology consulting company empowering leaders across the Life Sciences industries to make better data-driven decisions. Our data analytics and software platforms support data science, commercial operations, real world evidence, and cloud information management. We help to optimize business strategy and operations by delivering cutting edge analytics from the broadest set of data sources, combined with deep technical and domain expertise. We enable commercial excellence delivering analytical guidance to the field through SalesOps™, our cloud-based sales planning and operations platform. We are leaders in managing data using the latest cloud information management and big data technologies. We have more than 180 employees worldwide, are growing rapidly, and are proud to count a number of the top 10 global Life Sciences companies as our customers. We serve clients with a high-touch on-site and onshore presence, leveraged by a global delivery platform.

About Mirimus: Mirimus specializes in harnessing the power of RNA interference (RNAi) and CRISPR/Cas9 genome editing for cell and animal model creation for pre-clinical therapeutic development. Mirimus generates unique comparative gene-edited models for large pharma drug discovery groups and CROs. Mirimus is partnered with Charles River Laboratories and performs all of their custom mouse model creation for their North America GEMS division. Mirimus is also partnered with Biogen to develop novel RNAi therapeutics. Our mission is to provide superior preclinical models for target discovery and validation to accelerate therapeutic development for human health issues. About the Role: Mirimus is seeking a highly motivated, innovative and experienced full-time technician to contribute to their Genetically Engineering Service (GES) in the production of Animal Models and completion of research studies. Successful candidates will be part of an innovative and creative team with the opportunity to

Job Title: Sr Associate Clinical Contracts & Budgets Job Description Manage the end-to-end process for clinical site contracts and clinical trial-related consulting agreements, including contract amendments and termination letters. Prepare, negotiate, escalate, translate, distribute, obtain signatures, and archive contracts. Support site-related questions regarding invoice preparation and submission. Resolve contract and budget issues, manage contracting with local vendors, and maintain contract tracking in appropriate systems. Ensure payments are made in accordance with contracts and maintain payment data tracking. Provide information for entry into systems. Responsibilities + Negotiate site contracts using contract templates and collect necessary signatures for execution. + Negotiate site budgets and complete final budgets for inclusion in contracts. + Escalate contract and budget issues to Legal or Clinical Pricing Payments Group as needed to ensure Fair Market Value compliance. + S

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description AbbVie Data Science is the best-in-class team within its cross-industry peer group and is responsible for bringing people, process, and technology together to generate business value from clinical trials data. Our operational model is exemplified through execution and innovation. This role is a key to ensuring successful delivery against the program- and study-level accountabilities assigned to Data and Statistical Sciences. Responsibilities List u

PalletTrader is the leading digital marketplace and pallet management console, combining technology, industry expertise, and tailored managed services to revolutionize how businesses handle pallet needs. We offer both an online marketplace and fully managed solutions that streamline operations, enhance visibility, and reduce total cost of ownership. We are scaling fast and looking for a high-impact marketer who can own and optimize demand generation strategies that drive pipeline growth and revenue while aligning with our Go-To-Market (GTM) efforts. Role Overview: We’re looking for a data-driven, results-oriented Demand Generation/Marketing Manager to take ownership of multi-channel marketing programs that attract, engage, and convert valuable customers. This is a hands-on role focused on pipeline generation, lead nurturing, and campaign execution; while also contributing to strategy with the leadership team (you have a seat the table in this role). You won’t be alone in setting strate

Client: A leading Pharmaceutical Manufacturing (Product) Brand Work Location: Jersey City, NJ KEY ROLES AND RESPONSIBILITIES: Manage contracts and study budget Development of RFPs, selection of CROs/vendors Manage and lead cross-functional study teams in CRO, including vendors Development of study documents such as protocol, CSR, and publication materials Review of CRF and other operational materials, if required Provide accurate and up-to-date study information and study progression to manager or leadership and other stakeholders Communicate with investigators and investigative site staff WORK EXPERIENCE: Minimum 3-5 years of experience in late phase trials, IIT/Registry or Phase 4 study or similar role managing clinical trials, particularly in an IIT setting. Full cycle experience is a plus Strong clinical study management skills (including project and financial management) CRO/vendor management experience, including experience in audits and inspections Excellent communication skills