25 Clinical Research job postings in the Philadelphia, Pennsylvania area

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Job listings, help wanted ads and employment postings (last updated on Sunday, August 31)

Pharmacovigilance Safety Medical Writer

Monster.com

PA-Horsham, RESPONSIBILITIES: Ensure timely, quality deliverables for assigned tasks related to core deliverables with oversight as appropriate.
· Collaborate with PVER team members to perform assigned tasks, Interact with other stakeholders (eg, PVP, MSO) on relevant deliverables
· Initiate/conduct searches of internal and external databases
· Perform aggregate safety analysis and case level review
· Author/ … MORE INFO

Regulatory Affairs Associate

Monster.com

PA-Horsham, Requirements: - BS Life Sciences or Healthcare (or equivalent experience) - 1-2 Years of experience in Regulatory Affairs for a pharmaceutical company (may consider candidates coming from quality background too) - Experience with eCTD preferred - Experience working for a CMC group within Regulatory Affairs , preferably in the generic pharmaceutical industry, working with parenteral drug applicatio … MORE INFO

Regulatory CMC Associate

Monster.com

PA-Horsham, MUST HAVE: 2+ years Regulatory CMC experience in the pharmaceutical industry Experience evaluating/reviewing change controls from a regulatory perspective Experience compiling (not publishing) Annual Reports Responsibilities: Timely and thorough review of change controls in accordance to Guidance. Maintain compliance with regulatory requirements for pharmaceutical markets Focus is primarily on pos … MORE INFO

Project Assistant

Monster.com

PA-Warrington, This is an exciting opportunity for anyone that’s eager to start a career within the Clinical Research Industry. You will be introduced to how a clinical study is conducted and what’s required to support a clinical trial in an effort to bring a drug in development to market. Learn more about how you can be a part of Project Team that offers complete solutions for clinical trials. About the Project … MORE INFO

Medical Director

Monster.com

PA-Philadelphia, inVentiv Health — Transforming Promising Ideas into Commercial Reality Job Title: Medical Director Primary Function: The Medical Director supports the development and implementation of US Medical strategies, including US launch and lifecycle management. The focus of the role will be 50-60 percent internally facing and 40-50 percent external outreach, and will report to the product U. S. Medical Lea … MORE INFO

Director, Outcomes Research

Monster.com

PA-Gwynedd, The Director, USOR has the primary responsibility for planning and managing outcomes research (OR) activities for in-line and developmental drugs that are prioritized by the US Market Leadership Team. This includes all phases of outcomes research including design and implementation of retrospective database studies, assessment of patient reported outcomes, epidemiological studies and economic mode … MORE INFO

Clinical Development Lead, Neuroscience - MD

Monster.com

PA-Philadelphia, Primary Role: Under the direction and supervision of the Sr. Clinical Medicine Director, the Clinical Medicine Associate Director/Director is responsible for: • Participating on the Development Team as the Global Clinical Development Lead. • Providing medical and scientific support for products within the CNS therapeutic area. • Providing primary medical leadership and support to the clinical oper … MORE INFO

Global Clinical Development Lead - M.D.

Monster.com

PA-Philadelphia, Primary Role: Under the direction of the Sr. Clinical Medicine Director, the Clinical Medicine Director is responsible, with the project team, for Clinical development support including: • Providing input into the Clinical strategy (CDP) for assigned products • Drug Safety Assessments in Clinical Programs including medical monitoring, data review and or supervision of CRO medical monitors • Provid … MORE INFO

CLINICAL RESEARCH ASSOC, 1.0 FTE

Monster.com

PA-Philadelphia, Description Job Summary: The Clinical Research Associate is a professional person with a working knowledge of data management activities, communication skills, leadership ability, a willingness to cooperate as a team member who is responsible for the coordination of all activities relating to the Childrens Oncology Group. The Clinical Research Associate is also responsible for registration compila … MORE INFO

Director, Study Start Up

Monster.com

PA-North Wales, Study Start Up Director - Functional Excellence ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development — from compound selection to Phase I - IV clinical studies. We are currently recruiting for a Study Start up … MORE INFO

Clinical Data Lead II

Monster.com

PA-North Wales, If you have a background as a Clinical Data Leader combined with the know-how of managing large clinical trials, learn more about how you can be a part of a Data Management team that offers complete exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. A … MORE INFO

Assistant Director, Applied Data Analytics of HEOR (Remote Position)

Monster.com

PA-Philadelphia, Xcenda is a premier, full-service consultancy and leading managed markets agency. For more than 2 decades, global biopharmaceutical companies as well as emerging pre-commercialization phase firms have turned to Xcenda for strategic insights, health economics and outcomes research expertise, and reimbursement support. We help manufacturers successfully commercialize innovative medical treatments an … MORE INFO

Clinical Trial Specialist Lead

Monster.com

PA-North Wales, If you have extensive experience interpreting clinical trial protocols for the purpose of establishing and designing documentation requirements for a Trial Master File system, learn more about how you can be a part of ICON’s Document Management group that’s responsible for verifying clinical trial documentation is consistent with the TMF specifications, applicable SOPs, ICH/GCP guidelines and othe … MORE INFO

Pharmacy Specialist

Monster.com

NJ-Ewing, Pharmacy Specialist Prefers a Bachelor's degree from an accredited college or university in Health Care Management, Business or Pharmaceutical Administration. Requires two (2) years experience in third party prescription program claim adjudication. Requires two (2) years experience as a Pharmacy Utilization Management Specialist. Requires prior customer service/service quality initiative experienc … MORE INFO

Director, Outcomes Research - Respiratory

Monster.com

PA-West Point, Under the guidance of an Executive Director, Global Health Outcomes (GHO), the Director, Outcomes Research has the primary responsibility for planning and managing Outcomes Research activities for in-line and developmental Respiratory products and devices. Responsibilities include and are not limited to the following: All phases of outcomes research including design and implementation of retrospec … MORE INFO

Director, Outcomes Research-Osteo

Monster.com

PA-West Point, Under the guidance of an Executive Director, Global Health Outcomes (GHO), the Director, Outcomes Research has the primary responsibility for planning and managing Outcomes Research activities for Osteoporosis. Responsibilities include and are not limited to the following: All phases of outcomes research including design and implementation of retrospective database studies, assessment of patient r … MORE INFO

Laboratory Technician - Sequencing

Monster.com

PA-Philadelphia, Laboratory Technician — Sequencing Services Will work in our Sequencing Services/Molecular Biology offering section Performs Sanger sequencing for customer applications Conducts assays and lab procedures according to and in compliance with GLP, cGMP, CFR and/or PTC guidelines and SOPs. Accurately completes batch records and other required documentation according to and in compliance with GLP, cGMP … MORE INFO

Statistician

Monster.com

PA-King of Prussia, Job Number: 422577 Statistician Strategic Planning • Acquire detailed understanding of study design, execution and analysis of Sponsor Phase 2 and 3 cardiovascular studies with respect to objectives and the statistical implementation of those objectives with respect to: • Development (with data management) of a quality oversight plan • Critical Review of Study, DSMB, and integrated SAPs • Critical … MORE INFO

Clinical Scientist -Alzheimers

Monster.com

PA-Wayne, The Clinical Scientist participates in the development and delivery of clinical products/services related to clinical trials, such as training, surveillance, and cognitive testing. This Clinical Lead interacts with the sponsor to define the deliverables, and may directly participate in their execution through attendance at face-to-face and virtual training events. Clinical Responsibilities Develop … MORE INFO

Clinical Program Leader

Monster.com

PA-Wayne, Position Overview: The Clinical Program Leader is responsible for all aspects of clinical delivery for a portfolio of the client accounts and projects. S/he is responsible for clinical quality, clinical timelines, clinical task oversight, and clinical team performance across his/her assigned portfolio for the full project life cycle. The Clinical Program Leader will proactively build and maintain … MORE INFO

Project Manager with Immunoassay GLP

Monster.com

NJ-Princeton, Project Manager / Principal Investigator — Immunoanalytical in NJ Also seeking: Bioanalytical PM / PI for NC, NJ, Utah Also seeking: Immunoanalytical PM / PI for MD Also seeking: East Coast Business Development Director with Large molecule sales experience. Immunoanalytical Project Manager: Position Purpose: To manage the daily activities of immunoanalytical (pharmaceutical) studies. This position … MORE INFO

Research Investigator

Monster.com

NJ-Princeton, Requirements: -Ph. D. and/or M. D. in medicine, pharmaceutical sciences, engineering, or a related field, with 2-5 years of industry experience in clinical pharmacology/pharmacometrics, and proficiency with S-PLUS/R and NONMEM software. -Strong oral and written communication skills to clearly present scientific data, its interpretation and significance, and the ability to work in a dynamic scientifi … MORE INFO

CRAs –Looking for the best of the best! http://jobsearch.covance.com/47813-jobs.aspx

Monster.com

NJ-Princeton Township, Covance is looking for the “best of the best” CRAs. Oncology experience is needed. Are you looking for a career not just a position? Now is the time to join our growing business where you have supportive management and a cohesive team. At Covance, you are not just a number. We value you and your hard work. we want you to succeed. Covance is looking for CRAs who have oncology experience.
· $5,000 Sig … MORE INFO

Scientist

Monster.com

NJ-Skillman, Responsibilities: Excellent employment opportunity for a Scientist-I in the Skillman, NJ area. Will work with Raw Material Suppliers, Formulation and Manufacturing Process Subject Matter Experts, Toxicology and Regulatory on Governance of new and existing raw materials. The Project Coordinator will be responsible for collecting Raw Material Questionnaires from Chemical suppliers and ensure alignme … MORE INFO

Scientist

Monster.com

PA-Malvern, Responsibilities: Excellent employment opportunity for a Scientist in the Malvern, PA area. The scientist will be part of a team effort to provide cell banking services to PDMS, other R&D customers, company Chain and other clinical and commercial manufacturing sites. The scientist will perform cell culture according to Standard Operating Procedures using Good Manufacturing Practices. Primary respo … MORE INFO

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Employment information for Philadelphia, PA

5 year unemployment rate for
Philadelphia, PA (includes Philadelphia, Camden, NJ, Wilmington, and DE metro areas) - continue for more info

8.8%
Year
8.6%
Year
8.5%
Year
7.8%
Year
6.4%
Year

Updated to reflect Jul 2014 unemployment rates

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