Life Science Recruiter Salary at Precision Life Sciences Llc BETA

Proclinical is seeking a Global Labelling Development Lead to guide the labelling development for a key asset and oversee the Target Product Label initiative across our portfolio. Your expertise will also contribute to the labelling strategy of other assets as needed. This position can be based either in East Coast USA, Belgium or Switzerland. Responsibilities: Lead the labelling development strategy in cross-functional teams, considering target product profiles, competitor reviews, regulations, and development data. Create and maintain the target product profile for one asset from phase 2 to registration and for new indications of registered assets. Develop and manage the Core Company Data Sheet and collaborate with the Labelling Operation Manager on global labelling implementation plans. Support the US affiliate in creating and maintaining the USPI. Coordinate global labelling impact assessments for health authority or internal queries related to local label updates in post-marketing

Senior Manager - Contract - Remote, US Are you a dedicated professional eager to leverage your expertise in a fully flexible, remote position? Proclinical is seeking a Senior Manager, Feasibility to lead and manage study-level feasibility processes. In this role, you will focus on generating high-quality data to inform study design and operational planning within the oncology and biotechnology sectors. Primary Responsibilities: The successful candidate will collaborate with various teams to validate enrolment rates and timelines, support global trial optimization, and develop patient recruitment strategies. Skills & Requirements: Strong understanding of global clinical development programs. Effective communicator with diverse audiences. Ability to build strong team relationships. Experience using data to inform clinical strategies. Problem-solving skills for complex business questions. Experience in process development and change management. Creative and adaptable in dynamic environmen

Location: This role is based in the Lexington, MA area with a hybrid schedule of four days on-site and one day remote. We are looking for an experienced Senior Director of Quality Assurance to join a dynamic team. Reporting directly to the VP and Head of Quality, this role will be instrumental in developing, overseeing, and maintaining compliance standards across key third-party partnerships and within the organization’s internal Quality systems. This position holds primary responsibility for ensuring adherence to GMP protocols supporting product manufacturing and distribution, while also overseeing batch disposition processes for both clinical and commercial products. Key Responsibilities: Oversee the GMP Quality Assurance team to maintain quality and compliance standards. Develop and implement Quality objectives, managing risk and ensuring cross-functional compliance. Ensure quality control for manufacturing and distribution across clinical and commercial products. Manage compliance

PMO Lead - Contract - Framingham MA Ready to lead with impact? Proclinical are recruiting for a powerhouse PMO Lead to turn big ideas into flawless execution and results. Primary Responsibilities: This role will be required to lead and enhance project management office standards and processes. This role focuses on strategic alignment, risk management, and continuous improvement initiatives. Skills & Requirements: Bachelor's degree in engineering or a related field. Strong knowledge of project management methodologies such as Agile and Waterfall. Proven experience in managing projects and PMOs. The PMO Lead's responsibilities will be: Establish and maintain PMO standards, processes, tools, and training. Collaborate with project managers, stakeholders, and senior leadership for strategic alignment. Monitor project performance, identify risks, and implement corrective actions. Lead change initiatives to drive continuous improvement across the organization. Develop and implement PMO polici

HR Operations Manager – Biotech Location: Lexington, MA (Hybrid – 3 days onsite) Contract: 40 hours/week | 3–6 months We're hiring an Manager of HR Operations to lead critical people functions at the heart of our growing life sciences company. Reporting to the Chief People Officer, this is a strategic and hands-on role focused on building and scaling core HR operations that attract, retain, and support top talent. You’ll oversee compensation strategy, benefits administration, HRIS management, and HR compliance, while collaborating across teams to align programs with business goals. We’re looking for a technically strong, solutions-driven HR leader with a deep understanding of best-in-class practices, workforce analytics, and employee experience. What You’ll Do Lead compensation and benefits strategy, ensuring internal equity and market competitiveness Own and manage HRIS platforms and data integrity across systems Partner cross-functionally to support budgeting, financial planning, and

Manager, Site Start Up - Contract - Boston, MA We are on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world. Proclinical is seeking a motivated individual for the role of Manager, Site Start Up. Primary Responsibilities: The successful candidate will oversee the creation and management of site information within the CTMS system, focusing on institution details, personnel, and tasks related to site activation. You will be the primary contact for managing the Investigator and Institution Global Directory and play a key role in distributing Site Administrative Binders during site initiation. Skills & Requirements: Bachelor's degree in a relevant field. Experience in clinical operations, particularly in site start-up processes. Strong organizational and communication skills. Familiarity with CTMS systems and industry regulations. The Manager, Site Start Up's responsibilities will be: Capture and manage inv

Commercial SC Director - Permanent - Massachusetts Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that's shaping the future of healthcare and science. Proclinical is seeking a Commercial Supply Chain Director to lead strategic supply chain initiatives within the oncology and biotechnology sectors. Primary Responsibilities: The successful candidate will focus on developing and executing commercial planning processes to ensure successful product launches. The position requires collaboration with various teams to manage business relationships and optimize supply chain operations. Skills & Requirements: Bachelor's degree in life sciences or business. Experience in supply chain management within the biopharmaceutical industry. Proven ability to lead and develop teams and manage SRM and S&OP processes. Strong knowledge of supply chain systems and processes. Ability to influence and resolve conflicts across diverse teams. Skilled in strateg

Executive Director - Permanent - Philadelphia, PA We are on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world. Proclinical is seeking an Executive Director for Quality Control Operations in the gene therapy and pharmaceuticals sector. Primary Responsibilities: The successful candidate will focus on leading a team responsible for the testing and release of drug products and iPBMCs. You will oversee environmental monitoring, in-process, final release, and stability testing, ensuring all activities are efficient and compliant with regulations. This position requires strategic thinking and collaboration within a fast-paced environment. Skills & Requirements: Extensive leadership experience in commercial QC roles within the Pharmaceutical/Biotechnology industry. Strong preference for cell therapy experience. Proactive, results-oriented, and confident self-starter. Experience overseeing US and EU commercial