Senior manager clinical project planning jobs in the Biotechnology & Pharmaceuticals industry in Exton, Pennsylvania

ePharmaSolutions is an industry leading clinical trial technology & niche services provider to the life sciences industry. Our award winning eClinical solutions are used by more than 300,000 clinical researchers in 130 countries for the top 20 pharmaceutical companies and CROs in the world. We are again expanding our clinical operations department to include several Senior Clinical Project Manager...
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Principal Objective(s): The Senior Director, Clinical Development Operations is a key role for the strategic planning and implementation of clinical projects conducted by ViroPharma. The Senior Director, Clinical Development Operations will provide effective leadership, oversight and mentoring of the global clinical operations department thereby maximizing the potential of the global clinical oper...
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Principal Objective(s): The Senior Director, Global Clinical Pharmacology will provide scientific, technical and strategic leadership and expertise to the Clinical Pharmacology Department. This individual will have responsibility for the design and execution of all Clinical Pharmacology research and development activities. The individual will bridge activities and relationships stemming from bench...
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Job Description – Clinician, Scientific Affairs and Clinical Assessment LOCATION: Philadelphia Area SUPERVISOR: Director, Scientific Affairs and Clinical Assessment SUMMARY: TheClinicianis responsible for all aspects of assigned projects that include clinical assessment, training development and data review for Worldwide Clinical Trials, Inc. (WCT). The Clinicianworks under the direction of the Di...
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ePharmaSolutions is an industry leading clinical trial technology & niche services provider to the life sciences industry. Our award winning eClinical solutions are used by more than 300,000 clinical researchers in 130 countries for the top 20 pharmaceutical companies and CROs in the world. We are again expanding our clinical operations department to include several Clinical Project Coordinators w...
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Lead UBC project teams to deliver project milestones Specific Job Duties: o Oversee all aspects of trial conduct from Study start-up through close-out o Manage project per the scope of work and within the contracted budget o Ensure project is conducted according to UBC and client SOPs o Develop plans to achieve contracted milestones (i.e. project plan, clinical management plan, monitoring plan, tr...
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Clinical Project Manager We have a direct client in the Philadelphia area that is looking for a Clinical Project Manager a 12+ month project. · B.S. degree in nursing, pharmacy, or related health field, or experienced in healthcare; advanced is degree preferred. · 5+ years of project management experience · Understands and is compliant with Good Clinical Practices (GCPs), SOPs and study protocols....
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ePharmaSolutions is an industry leading eClinical solutions & niche services provider to the pharmaceutical industry. Our award winning Clinical Trial Portal is used by more than 300,000 clinical researchers in 130 countries for the top 20 pharmaceutical companies in the world. Our company is experiencing tremendous growth due to accelerated adoption of our eClinical solutions and niche clinical s...
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Clinical Data Manager Quality Data Services, Inc., a highly respected Clinical Research Organization in King of Prussia, PA, is seeking a Clinical Data Manager to manage the timely and quality completion of databases of clinical studies contracted to Quality Data Services, Inc (QDS), manage internal data management and database development staff, and act as liaison with sponsor and/or third-party ...
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The Senior Clinical Programming Specialist follows established standards and procedures to provide a wide range of clinical programming duties involving designing, developing, evaluating and modifying computer programs to analyze and evaluate clinical data. The position will develop activities within the scope of a project. Major Duties and Responsibilities: Follows established procedures for deve...
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Principal Objective(s): Work within ViroPharma to oversee the management of Phase I through IV clinical research studies conducted in Emerging Market countries to ensure compliance with regulatory requirements (e.g. GCP/ICH), overall quality study conduct and adherence to study timelines. Major Duties and Responsibilities: Identification, selection and oversight of Phase I-IV Clinical Research sit...
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Clinical Data Manager Job summary The Clinical Data Manager will act as a liaison with project managers and Data Managers at pharmaceutical companies and CROs, from protocol development to completion of a clinical drug or device development program. The core responsibility involves working with eCaseLink project managers to develop Case Report Forms, edit specifications, user acceptance testing, e...
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Job Description – Clinical Manager, Scientific Affairs and Clinical Assessment LOCATION: Philadelphia Area SUPERVISOR: Director, Scientific Affairs and Clinical Assessment SUMMARY: TheClinical Manageris responsible for all aspects of assigned projects that include clinical assessment, training development and certification for Worldwide Clinical Trials, Inc. (WCT). The Clinical Managerworks under ...
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Job Title: Clinical Imaging Associate Position Responsibilities Conduct set-up of clinical trials within the internal imaging system under limited supervision Proactively participates in a partnership with the matrix partners Ensure trials are validated before going live Understand financial drivers and their role in decision making Ensures that the conduct of imaging work meets GCP requirements C...
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BioClinica, Inc. is currently recruiting for an experienced Clinical Data Manager. This position is located in our Audubon, PA office. The Clinical Data Manager is responsible for supporting clinical trials for clients using our proprietary electronic data capture and/or IVR products. The CDM will create and/or authorize the data management plan, define and validate edit checks, and perform clinic...
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Principal Objective(s): The Clinical Data Associate at ViroPharma Incorporated follows established standards and procedures to provide a wide range of clinical data management duties to ensure the accuracy and completeness of clinical trial data. Major Duties and Responsibilities: Follows established GCP procedures and practices for implementing and maintaining processes to assure departmental goa...
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Our client has an immediate opening for a Sr Statistical Programmer to work as a member of their Biometrics Department. You will provide statistical support for Phase 1-3 clinical studies. The candidate will closely collaborate with project teams consisting of clinicians, project managers, statisticians, data management and other functions. Activities include reviewing statistical section of the p...
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The Senior CRA (SCRA), is responsible for management of the day-to-day aspects of Investigator site and Clinical Research Associate activities for the assigned study or studies. The SCRA, in concert with the Project Leader, is accountable for the timely, quality, satisfactory, and cost-effective completion of the client’s study. The SCRA may manage a single service, monitoring only the study or as...
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Clinical Research Associate w/PM Experience Keystone Computer Associates is a Minority-owned Business Enterprise (MBE) and a leading vendor for IT, professional and pharmaceutical staffing and recruiting services. Keystone has been in business since 1965 and is headquarted in Fort Washington, PA. We are currently searching for a high-level, in-house Clinical Research Associate with Project Managem...
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Our client is currently seeking a qualified Infrastructure Manager to join their growing IT group. Job Purpose • Provide enterprise-wide IT Infrastructure support for a global pharmaceutical organization • Lead the enterprise effort in support of the company’s help desk, server/ network/desktop/information security, and application systems and processes • In support of critical business capabiliti...
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Lead UBC Pharmacovigilance project teams to deliver project milestones Specific Job Duties: o Oversee all aspects of the safety project conduct from Start-up through Close-Out o Manage project per the scope of work and within the contracted budget o Review contracts and ensure that change orders are issued, as necessary o Ensure project is conducted in concert with UBC SOPs, project-specific proce...
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Sr. Statistical Programmer Come grow with us! Frontage, a CRO is experience tremendous growth and is seeking a talented Sr. Statistical Programmer to join our team in Exton, PA. Responsibilities: Candidate, as a member of Biometrics Department, will provide statistical support for Phase 1-3 clinical studies. The candidate will closely collaborate with project teams consisting of clinicians, projec...
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Sr. Statistician Come experience the growth. Frontage is a global, integrated contract research organization (CRO) serving clients within pharma and biotech companies. With headquarters in Exton, Pennsylvania, near Philadelphia, and a division in Shanghai, China, we offer drug R&D services that combine unmatched quality, speed, and value. This role is based in our Exton, PA, Headquarters. Responsi...
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Johnson & Johnson companies are equal opportunity employers. Associate Director Market Access-8171130114 Description DePuy Synthes, a member of the Johnson and Johnson Family of Companies, is recruiting for an Associate Director, Market Access, located in Westchester, PA DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic and neurological busi...
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Johnson & Johnson companies are equal opportunity employers. Senior Supervisor - Manufacturing-7814130604 Description Janssen Biotech Inc., a member of Johnson & Johnson&'s family of companies, is recruiting for a, Sr. Supervisor Manufacturing, located in Malvern, PA. For more than 30 years, Janssen Biotech, Inc. has delivered on the promise of new treatments and ways to improve the health of indi...
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