Beacon Hill Legal is seeking a Clinical Trials Project Manager for a global biotechnology company in the greater Philadelphia region. This long-term temporary position involves managing clinical trial studies in the life sciences industry, including reviewing, drafting, and negotiating clinical trial agreements, consulting agreements, CDAs, and ICFs. The role requires coordination with the budget team, tracking study timelines, and overseeing specialists involved in studies.

Clinical Trial Contracts Manager

Clinical Trials Project Manager

The Clinical Team Leader at Deborah Heart and Lung Center is responsible for the 24-hour operation of assigned patient care unit(s), including patient care and nursing services assessment, planning, provision, and evaluation. This role also involves participation in the department's nursing services assessment, planning, provision, and evaluation, as well as providing on-call shift supervision coverage as assigned.

RN - CLINICAL TEAM LEADER

Clinical Team Leader

Participate in clinical trials to earn additional income, sometimes from the comfort of your home. This role involves getting paid to trial new treatments and medications, contributing to science, and potentially receiving free access to cutting-edge medical treatment.

NO EXPERIENCE: HIGH PAID CLINICAL TRIALS FOR MENTAL OR PHYSICAL CONDITIONS

Clinical Trial Participant

The company is seeking a dedicated MD or DO to join their team as a Principal Investigator for clinical trials in women's health. This role is ideal for a full-time physician looking to diversify their income and provide additional support to their patients through clinical research. The position offers a flexible time commitment, competitive compensation, and the opportunity to enhance patient care through participation in cutting-edge clinical research.

Principal Investigator (MD/DO) for Clinical Trials

Principal Investigator for Clinical Trials

The Clinical Trial Associate (CTA) will work with the Clinical Operations team to support the conduct of clinical trials. This role involves supporting various clinical trials and managing certain aspects of the clinical trials, partnering with Clinical Project Managers and Clinical Trial Managers to ensure studies are completed on time, within budget, and in compliance with SOPs, FDA regulations, and ICH/GCP guidelines. This is a fully remote, contract position with a duration of 6 months.

Clinical Trial Associate 100% Remote

Clinical Trial Associate

Johnson & Johnson is seeking an Associate Director, Clinical Project Scientist for Oncology in Horsham, PA. This role involves implementing Investigator Initiated Studies (IIS), collaborative group studies, and company sponsored studies, including both interventional and registry studies. The candidate will work closely with US Hematology Medical Affairs Oncology teams and Global Development partners to execute, track, manage, and oversee approved protocols. The focus is on ensuring appropriate execution to deliver data that supports evidence generation needs in the US, acting as a point of contact with external Investigators and collaborative groups.

ASSOCIATE DIRECTOR, CLINICAL PROJECT SCIENTIST

Associate Director, Clinical Project Scientist

The Clinical Research Coordinator (CRC) is a specialized research professional under the direction of the clinical Principal Investigator and Site Manager, responsible for supporting, facilitating, and coordinating the daily clinical trial activities. This role is crucial in the conduct of clinical trials, including patient recruitment, enrollment, scheduling, and maintaining GCP and protocol standards. The position offers a pathway for career advancement within the company.

Clinical Research Coordinator

The Lead Research Scientist at the Institute for Health Metrics and Evaluation (IHME) will drive analytic innovation, supervise and mentor junior staff, and participate in leadership responsibilities for the Future Health Scenarios team. This role involves managing research team staff, developing custom scenarios for future health outcomes, and presenting results to various audiences. The position requires a strong command of forecasting models, the ability to supervise and mentor junior staff, and a commitment to improving health outcomes globally.

Lead Research Scientist, Future Health Scenarios

Lead Research Scientist

The Clinical Research Associate at Ascendion is responsible for managing clinical activities at study sites, fostering strong relationships within the organization, and overseeing the performance of appointed study sites. This role involves conducting site visits, monitoring, communication, and delivering on assigned study sites, serving as a liaison between Clinical Operations and study site personnel.

Clinical Research Associate

The Clinical Proposals & Feasibility Lead at Actalent is responsible for managing and creating Proposal & Feasibility strategy for assigned projects, focusing on the North American market. This role involves assisting Operations/Business Development with the generation of proposals, supporting client interactions, and long-term strategic partnerships. The position is remote, part-time, starting with 20 hours per week, and requires a preference for EST time zone.

Clinical Proposals & Feasibility Lead

The Clinical Research Coordinator in Media, PA is responsible for overseeing the execution of study protocols under the guidance of the Principal Investigator. This role involves handling participant-related tasks, including scheduling and conducting visits, documenting study procedures, collecting vitals, and performing phlebotomy/specimen collection. The coordinator will also manage data and communicate with sponsors, requiring travel up to four times a year for new study start-up activities.

Clinical Research Coordinator - 232670

As a Clinical Trial Manager II at ICON Clinical Research, you will be responsible for managing and prioritizing clinical deliverables to ensure they meet quality and regulatory requirements, project timelines, budget, and sponsor expectations. This role involves creating and administering clinical and site training plans, maintaining knowledge of contract details, and overseeing the filing of study and site level essential documents. You will also play a key role in risk management, quality standards compliance, and effective communication with various stakeholders.

Clinical Trial Manager II

The Manager of Clinical Trial Strategy and Submissions at AbbVie is responsible for delivering regulatory strategies and operations for a designated portfolio of development compounds globally. This role involves ensuring compliance with global regulatory strategies, managing study deliverables, interfacing with regulators and global subject matter expert functions, and maintaining regulatory databases. The position can be based remotely within the US.

Manager, Clinical Trial Strategy and Submissions (Remote)

Manager, Clinical Trial Strategy and Submissions

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Clinical Trials Leader Jobs in Collegeville, PA Hiring Now

Clinical Trial Contracts Manager

RN - CLINICAL TEAM LEADER

NO EXPERIENCE: HIGH PAID CLINICAL TRIALS FOR MENTAL OR PHYSICAL CONDITIONS

Principal Investigator (MD/DO) for Clinical Trials

NO EXPERIENCE: HIGH PAID CLINICAL TRIALS FOR MENTAL OR PHYSICAL CONDITIONS

Clinical Trial Associate 100% Remote

ASSOCIATE DIRECTOR, CLINICAL PROJECT SCIENTIST

Clinical Research Coordinator

Lead Research Scientist, Future Health Scenarios

Clinical Research Associate

Clinical Proposals & Feasibility Lead

Clinical Research Coordinator - 232670

Clinical Trial Manager II

NO EXPERIENCE: HIGH PAID CLINICAL TRIALS FOR MENTAL OR PHYSICAL CONDITIONS

Manager, Clinical Trial Strategy and Submissions (Remote)