Clinical Jobs in Upper Darby, PA
Outlier
$25 - $45 HOUR
Philadelphia, PA
Outlier is looking for talented Clinical Medicine Experts to help train generative artificial intelligence models. Currently, pay rates for core project work by Clinical Medicine experts range from $25 to $45 per hour USD.
Outlier
$25 - $45 HOUR
Wilmington, DE
Outlier is looking for talented Clinical Medicine Experts to help train generative artificial intelligence models. Currently, pay rates for core project work by Clinical Medicine experts range from $25 to $45 per hour USD.
EPM Scientific
King Of Prussia, PA
Responsibilities: Spearhead the creation and documentation of business and system requirements at the study level in collaboration with internal stakeholders and technology vendors. Lead the governance and oversight of IxRS, Imaging, ECG, eCOA, and other Clinical Technology suppliers.
Slone Partners
Horsham, PA
Under the direction of the Laboratory Director of Record, this leader is involved in the planning, development, and implementation of new and improved laboratory methods, as well as approving them before implementation. Additionally, the Lab Director may be assigned specific quality-based SOPs to ensure compliance with accrediting bodies and may interact with clients to address issues within their scope.
Trinity Health
Philadelphia, PA
Trinity Health Mid-Atlantic Medical Groups is currently seeking board certified or board eligible Family Medicine, Internal Medicine, or Med-Peds physicians to join our established and new outpatient Primary Care practices located in the greater Philadelphia area, Pennsylvania. Trinity Health Mid-Atlantic Medical Groups has over 75 office locations offering a diverse network of primary care and specialty services including cardiovascular, oncology, maternity, orthopedics, pain management, sports medicine, and neurosurgery.
TalentBurst, Inc.
$80 - $93 HOUR
Philadelphia, PA
Identify research process deviations and raise issues or risks when discovered, providing hands-on support to the Epic Clinical Trials Billing Team and research study teams; assisting with on-going knowledge transfer and training of Clinical Trials Specialists/Billers. The Clinical Trials Building Analyst must complete and maintain the following EPIC coursework to be eligible for this position: pre-reqs: GEN006, GEN606, PRE051 and PRE052.
Planet Pharma
King Of Prussia, PA
ESSENTIAL DUTIES AND RESPONSIBILITIES: • In collaboration with the clinical study teams for a specific product candidate in clinical development, designs, prepares and initiates study protocols and other required documentation in compliance with project plans, federal regulations, GCP and good medical practice. • Collaborates with team members in clinical review and interpretation of study data in support for preparation of reports for health authorities including regulatory filing documentation and study close-out reports.
AMN Healthcare
$210000 - $275000 YEAR
Philadelphia, PA
At AMN Healthcare, we strive to be recognized as the most trusted, innovative, and influential force in helping healthcare organizations provide quality patient care that continually evolves to make healthcare more human, more effective, and more achievable. The Department of Clinical Genetics at Fox Chase Cancer Center Seeks a Medical Oncologist | Access Unparalleled Research Support | Balance Clinical and Research Roles | Live and Work in Highly Desirable Philadelphia.
Kelly Science, Engineering, Technology & Telecom
Horsham, PA
The Business and Contract Operations Coordinator will support the Business Strategy and Contract Operations Leaders in partnering with Medical Affairs and staff to drive the coordination of activities necessary to meet cross-Therapeutic Area research and operational objectives and timelines (e.g., Global concept and protocol reviews, HCC reviews, CPC documentation and support, contracting, budget tracking, etc.), including interacting with associated systems (Totality, Gensight PMT, Sharepoint, MS Teams, ReCAP, ICD, eMarketplace, Icertis, Aravo). This is a key coordinating role to ensure compliance with company and departmental policies and processes, primarily in support of at least one functional areas across Medical Affairs and other JSA departmental teams (i.e. DMI, VESE, CHME,MISE REMS, RW Indirect) contracting/procurement process and support, and health care compliance review.
Eisai
Philadelphia, PA
Independently conduct Clinical Investigator Site Audits, GCP Document Audits (Clinical Study Reports and Trial Master Files), internal Process Audits and support Vendor/System audits. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States.
SQRL
$55000 - $65000 YEAR
Plymouth Meeting, PA
While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical trial process! Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best-in-class experience for patients and sponsors.
Clinical Management Consultants Careers
Cherry Hill, NJ
Your role will involve developing and implementing cutting-edge educational programs, ensuring that our NICU nurses are equipped with the latest knowledge and skills to provide exceptional care. Located near the charming area of Northwest New Jersey, our hospital offers the Night NICU Nursing Clinical Educator not only a top-notch working environment but also a fantastic place to live.
Jobot
$350000 - $400000 YEAR
Philadelphia, PA
This position will play a key role in the biopharma industry, assisting with the development and implementation of clinical strategies and protocols across metabolic diseases. 2. Assist in the design and execution of clinical trials, including the development and review of study protocols, case report forms, and other study-related documents.
Clinical Management Consultants
Cherry Hill, NJ
Your role will involve developing and implementing cutting-edge educational programs, ensuring that our NICU nurses are equipped with the latest knowledge and skills to provide exceptional care. Located near the charming area of Northwest New Jersey, our hospital offers the Night NICU Nursing Clinical Educator not only a top-notch working environment but also a fantastic place to live.
CSL Behring
King of Prussia, PA
Ability to proactively identify, analyze, and effectively explain potential legal risks and complex legal issues to clients and develop creative and business-focused advice and solutions in order to facilitate the business objectives of the company while effectively managing risk. Reporting to the Lead Counsel, Global Clinical Legal, as the Counsel, Clinical Legal, you will collaborate with the Global Clinical Development, provide practical, timely, and high-quality legal support to CSL's Global Clinical Development function on a wide range of legal and regulatory issues.
CSL Behring
King of Prussia, PA
Ability to proactively identify, analyze, and effectively explain potential legal risks and complex legal issues to clients and develop creative and business-focused advice and solutions in order to facilitate the business objectives of the company while effectively managing risk. Reporting to the Lead Counsel, Global Clinical Legal, as the Counsel, Clinical Legal, you will collaborate with the Global Clinical Development, provide practical, timely, and high-quality legal support to CSL's Global Clinical Development function on a wide range of legal and regulatory issues.
Planet Pharma
Philadelphia, PA
Perform site co-monitoring visits at various timepoints in the study (selection, initiation, monitoring and close-out visits) to ensure CRAs working for the CRO on behalf of the sponsor, are monitoring in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. The Sponsor CRA is responsible for monitoring oversight, co-monitoring, and site management work to ensure that the CRAs working under the CRO(s) and the sites conducting the studies on behalf of our client, follow all applicable regulations, guidelines, and sponsor requirements.
Mitchell Martin
$35 HOUR
Philadelphia, PA
Track and ensure timeliness and clinical appropriateness of the documentation and necessary paperwork related to all case activity of his/her supervisees (such as assessments, CBE/CBR documents, initial treatment plans, treatment plan reviews, discharge summaries, aftercare plans, progress notes, concurrent reviews and treatment authorization requests). The Children's Mobile Intervention Services (CMIS) Clinical Supervisor oversees staff, which includes a team of Intervention Specialists, Mental Health Case Managers and a Family Support Partner to ensure that quality services are being delivered by staff in compliance with program timelines and clinical guidelines.