Alpha Consulting Corp.

RESEARCH ASSOCIATE: TISSUE / CELL CULTURE CAMBRIDGE, MA Position will be onsite . Required Skills: Bachelor's degree in biology with at least 3 years' relevant work experience or master's degree with at least 1 year of academic/industrial experience in cancer biology/oncology or immune oncology. Manager is looking for non-PhD candidates. Looking for master's or bachelor's degree with 3 to 5 years' experience in Biotech/Pharma or hospital setting. Hands-on experience in isolation, culture, and characterization of primary cells from human or animal tissues is required. Experience executing biochemical assays with a variety of readout technologies, including flow cytometry and ELISA is required. Excellent communication, presentation, collaboration, and organizational skills are required. Ability to execute and operate to a high standard. Attention to detail with excellent organizational and record keeping skills is a requirement. Ability to identify technical problems and potential solutions. Proficiency in utilizing software such as Graph Pad, Microsoft Office, etc. for data analysis and figure generation is required. Tissue culture and Cell culture experience. Technical/biological Duties: Cell culture and cell-based assays. Primary cell isolation from whole blood and tissues. Cytokine detection experiments using multiplex assay technologies. Execute complex biochemical assays, including RNA/DNA isolation, real-time PCR, protein isolation and immunoblotting. Preferred Skills: Flow Cytometry experience is a plus. Research experience in cancer biology and cancer immunotherapy is highly desirable. Project Description: We are currently seeking a highly motivated associate scientist to join our cancer biology group in Cambridge, MA. The successful candidate must demonstrate technical expertise in cellular and/or molecular biology assays to validate therapeutic targets and perform mechanism of action studies to support programs as they enter and move through clinical development. This 12+ month position starts ASAP. Please E-MAIL your resume (attachment to email) with rate and availability to Jim: ALPHA'S REQUIREMENT #21-03861 W2 ONLY MUST BE ELIGIBLE TO WORK IN THE U.S. AS AN HOURLY W2 EMPLOYEE #LI-JP1 - provided by Dice

VENDOR & OUTSOURCING MANAGEMENT WITH PHARMACEUTICAL / CLINICAL LAWRENCE TOWNSHIP, NJ Will start remote, move to onsite 2-3 days a week once restrictions are lifted. (Expected Oct 2021) Project Description: The Clinical Trial Business Partnering (CTBP) department is focused on executing the business' sourcing strategy across all phases of R&D development operations. This group applies a common framework to drive efficient, consistent and compliant processes for vendor relationship and management of the Client's major clinical service providers. Serving as a bridge between the Client's clinical teams and external services providers, the Vendor & Outsourcing Management group within CTBP is responsible for building the appropriate in-house management/oversight structure and mechanisms, while driving the external collaboration with clinical service providers in effort to yield a multitude of innovative ideas to deliver on the Client's goals. This position reports to the Director of Global Outsourcing Management. As an integral member of CTBP, the Outsourcing Manager is the process gatekeeper and expert related to outsourcing processes. Duties/Responsibilities: Provide operational expertise and strategic leadership, support, guidance and training to teams on all aspects of outsourced work. Ensure alignment of teams to the related Client's outsourcing strategies. Drive outsourcing activities by interfacing with operational teams, support groups and service providers for successful selection, contracting and execution of outsourced studies while ensuring compliance with regulatory standards, ethical practices, the Client's outsourcing and procurement policies and procedures. Required Skills: Degree in Legal, Life science, Business Administration or equivalent. Advanced degree a plus. Clinical development experience of 3 to 5 years required, with Scientific, Financial and Project management experience desired. Experience interacting with a wide range of suppliers (e.g., Contract Research Organizations, Cooperative groups, Clinical laboratories, Core laboratories including ECG and Imaging service providers): initiating, negotiating and executing legal and/or financial agreements in the clinical trials environment- biotech or pharmaceutical industry. Proven experience in managing key internal and external stakeholders effectively by frequently soliciting input and gathering and incorporating feedback into processes as appropriate. Effective management of cross-functional, multi-cultural teams and demonstrated ability to work and influence within a matrix structure. Proven time management skills and ability to be flexible to meet job demands and take on new initiatives and improvement efforts. Ability to sustain high levels of performance in a constantly changing environment. This 6+ month position starts ASAP. Please E-MAIL your resume (attachment to email) with rate and availability to Bridget: ALPHA'S REQUIREMENT #21-03010 MUST BE ELIGIBLE TO WORK IN THE U.S. AS AN HOURLY W2 EMPLOYEE #ZR #LI-BB1 - provided by Dice

CLINICAL PROJECT COORDINATOR LAWRENCEVILLE, NJ Position may start remoted then be onsite 2-3 days a week (expected Oct 2021) Project Description: The candidate will be responsible for assisting in processes related to the Client's TSE (Transmissible Spongiform Encephalopathies) program. Develop an in-depth knowledge of global TSE requirements and be able to apply these requirements to the job. Maintain TSE information repositories within the Client. Effectively network within key business partners to achieve assigned objectives. Evaluate documentation for compliance to current requirements and help with securing documentation for the preparation of the Client's TSE Regulatory Compliance product statements. Required Skills: Top 5 must have skills: cGMP Knowledge 3+ years with MS Office 365 TSE/BSE Knowledge . Biologics experience is preferred. Bachelor's Degree Job Requirements/Education: Excellent oral and written communication skills. Proficient navigation of electronic systems, (e.g., MS Excel, and Adobe Acrobat) including formatting and electronic management of data and information. The candidate must have demonstrated ability to be a strong team member with the ability to drive projects to completion on time. Knowledge of global BSE/TSE regulations and guidances a plus. Knowledge of product formulation and manufacturing processes desirable. Ability to handle multiple projects and prioritize work independently. Basic understanding of the drug development process plus an integrated view of the technical, manufacturing and commercial aspects of the pharmaceutical business. Minimum of 2-5 years of experience in the pharmaceutical industry with a BS degree in a scientific discipline, chemistry or pharmacy preferred. Experience in GMP auditing and/or CMC regulatory a plus. This 6+ month position starts ASAP. Please E-MAIL your resume (attachment to email) with rate and availability to Bridget: ALPHA'S REQUIREMENT #21-03014 MUST BE ELIGIBLE TO WORK IN THE U.S. AS AN HOURLY W2 EMPLOYEE #ZR #LI-BB1 - provided by Dice

DIGITAL PROJECT MANAGER CLINICAL INFORMATICS (REMOTE) BOSTON, MA 100% remote with some travel to the Boston office Project Description: As a Digital Clinical Project Manager, you will be spearheading the execution of critical digital projects in support of our ambitious clinical digital roadmap. In this role, you will connect and lead various stakeholders and contributors to collaborate on digital clinical projects. Define and Lead Digital Clinical Projects. Coordinate and participate in requirement gathering and definition (Business Analysis). Establish and manage project timelines. Ensure project goals and means meet business objectives and deliver value in a timely fashion. Work collaboratively across the organization to gain alignment on project objectives and deliverables. Engage with Computer Systems Validation lead to support appropriate validation activities. Report on project progress and status. Required Skills: 7+ years' experience in digital project management in a GxP environment . Proven experience with numerous Clinical, Data Management, Regulatory and Pharmacovigilance systems. Veeva experience preferred. Working knowledge of CSV concepts for SaaS GxP applications . Tangible track record in using Agile approaches in a regulated environment . As a technologist, you know your craft and, you are fluent in the digital world. You have first-hand knowledge of SaaS technology in a GxP environment and practical understanding of data integrity requirements for systems used in the conduct of clinical trials. You have a working knowledge of clinical operations, clinical data management, regulatory and safety business processes in a drug development context. You work independently yet engage proactively with team members, colleagues and stakeholders to get alignment and drive projects forward. You don't hesitate to dive in and work alongside your team. You can effectively manage conflicting priorities in a fast pace environment, and you can navigate ambiguity and lead a team effectively . You put team before tasks by collaborating actively with all team members and supporting them. Bachelor's degree in Computer Science, Biotechnology or equivalent required. Master's preferred. This 6+ month position starts ASAP. Please E-MAIL your resume (attachment to email) with rate and availability to Bridget: ALPHA'S REQUIREMENT #20-00945 MUST BE ELIGIBLE TO WORK IN THE U.S. AS AN HOURLY W2 EMPLOYEE #ZR - provided by Dice