39 Clinical Research job postings in the Philadelphia, Pennsylvania area

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Job listings, help wanted ads and employment postings (last updated on Friday, January 30)

Clinical Research Associate (CRA) Level II - Home Based East Coast

Monster.com

PA-Philadelphia, This is a home-based position in AL, AR, CI, DE, DC, FL, GA, KY, LA, ME, MD, MA, MS, NH, NJ, NY, NC, OH, PA, RI, SC, TN, VT, VA and WV. PPD - Local Community. Global Reach. Our global team of experienced CRA Managers work to ensure that our CRAs have an appropriate work load, the tools they need to be successful and that there is a plan for their continued career advancement. PPD CRAs also enjoy b … MORE INFO

Biostatistician II

Monster.com

PA-Horsham, PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed sig … MORE INFO

Senior Clinical Data Programmer

Monster.com

PA-Warrington, If you have a background in clinical data management combined with experience of extracting clinical data from electronic Case Report Forms (eCRF), learn more about how you can be a part of growing Clinical Research Organization that offers continued growth in the field of Data Management. About the Senior Clinical Data Programmer role within ICON: The Senior Clinical Data Programmer will be respo … MORE INFO

Director, Business Development - East Coast

Monster.com

PA-Philadelphia, If you’re interested in working for a Leading, Mid-Size Contract Research Organization (CRO) that has a massive global reach, then look no further, because Pharm-Olam International offers all of that and more! We are a company that strives to deliver cost-effective, quick-to-market clinical services in today’s emerging marketplace. Pharm-Olam International has one of the largest global footprints … MORE INFO

Operations Manager

Monster.com

PA-North Wales, Are you interested to drive client relationships and business processes within DOCS — ICON’s leading provider of Resourcing Solutions to the Clinical Trials Industry? Operations Manager role within DOC’s: Founded in 1997, DOCS has grown to become the premier staffing provider to the clinical development industry. The company was acquired by ICON plc. in 2007 and was merged with ICON’s existing res … MORE INFO

Senior Business Analyst

Monster.com

PA-North Wales, “At ICON, it's our People that set us Apart” The Senior Business Analyst a critical clinical role providing support and metrics analysis across projects delivered to our Sponsors within the Firecrest organization! Senior Business Analyst role within ICON: ICON has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clin … MORE INFO

Senior Manager Sponsor Solutions

Monster.com

PA-North Wales, “At ICON, it's our People that set us Apart” Are you interested cultivating sponsor solutions and building strong relationships with ICON business development and client teams? Senior Manager, Sponsor Solutions role within ICON: ICON has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing serv … MORE INFO

eClinical Specialist (ePRO)

Monster.com

PA-King of Prussia, Job Title: eClinical Specialist (ePRO) Position Description The e-Clinical Specialist is an integral role within the Clinical R&D Business Technology team Timely availability of clinical data is a key requirement for the global CRD organization, which allows informed decisions to be made as early as possible The e-Clinical Specialist will report into the e-Clinical Manager who is responsible for t … MORE INFO

Project Publications Lead

Monster.com

PA-Wayne, Job Title: Project Publications Lead Position Responsibilities Track and Report Global Publications Performance. Define publication strategy with Global Medical Affairs stakeholders for one or more publication projects. Develop and implement strategic and in-year tactical publication plans for one or more publication projects. Support the definition, development and implementation of an integrated … MORE INFO

Clinical Documentation Specialist

Monster.com

PA-Wayne, Job Title: Clinical Documentation Specialist Position Description Reporting to the Clinical Documentation Team Lead, the Clinical Document Specialist is responsible for the management of clinical study records (e. g. clinical Trial Master File) from set up through to final archival, ensuring compliance with company SOPs and process. With a focus on inspection readiness, monitors clinical Trial Mast … MORE INFO

Clinical Documentation Specialist

Monster.com

PA-Wayne, Job Title: Clinical Documentation Specialist Position Description Reporting to the Clinical Documentation Team Lead, the Clinical Document Specialist is responsible for the management of clinical study records (e. g. clinical Trial Master File) from set up through to final archival, ensuring compliance with company SOPs and process. With a focus on inspection readiness, monitors clinical Trial Mast … MORE INFO

Pharmacovigilance Specialist

Monster.com

PA-Wayne, Job Title: Pharmacovigilance Specialist Position Responsibilities Conducting pharmacovigilance case reconciliation with business partner, patient support programs and market research. Request/create reconciliation monthly data, send monthly data and/or request monthly data from other parties and manage responses. Interact with PV personnel to resolve any outstanding cases that cannot be reconciled … MORE INFO

Senior Clinical Data Manager

Monster.com

PA-Media, Sr. Clinical Data Manager Requirements: - BS or Nursing Degree - Must have strong CRO experience. - 3-5 years of data management experience in clinical research environment (ideally a smaller, hands on CRO, pharmaceutical, biologics, or medical device company) with at least one year of data manager experience - Experience acting as a project manager/team lead managing studies from preparation thro … MORE INFO

Automation Specialist - Pharmaceutical

Monster.com

NJ-Princeton, Automation Specialist Automation Specialist with Hamilton Star and Starlet, Tecan or other automation robotics. Program and be able to modify the automation programs Perform maintenance and calibration Set up assays on the Hamilton Good instrument validation skills under GLP Contact Melissa at Melissa@sageinc. net 732 337 0864 … MORE INFO

Sr. Bioanalytical Lc/ms/ms Project Manager / Principal Investigator

Monster.com

NJ-Princeton, Senior Project Manager Lc/ms/ms - NJ Project Manager Lc/ms/ms — NJ, NC, Utah Also seek Lc/ms/ms Scientist — NJ Minimum of a Bachelor’s degree in the Natural Sciences or Associates degree with equivalent experience. Good understanding of Lc/ms/ms , GC, mass spectrometry and bioanalytical methods and a thorough understanding of GLP guidelines and Bioanalytical Division SOPs and practices. Ability to … MORE INFO

Research Scientist or Bench Scientist with ELISA

Monster.com

NJ-Princeton, Research Scientist or Bench Scientist The major duties and responsibilities of a Research Scientist include the following: 1. Follows all standard operating procedures, safety and security polices and prescribedGLP and Biomarker and Immunoanalytical Division practices, policies and guidelines; use SOP manual as reference to support work performed. Completes all necessary paperwork related to job d … MORE INFO

Clinical Research Quality Assurance Specialist

Monster.com

NJ-Berlin, Works with Regulatory affairs to identify and interpret regulations, guidelines, and other pertinent information issued by applicable regulatory agencies and other regulatory organizations. Review protocols, consent forms, source documentation, and CRFs as appropriate for various clinical research projects to ensure study team compliance with sponsor protocols and site SOPs. Identifies needed proc … MORE INFO

Study Start-Up Specialist II

Monster.com

NJ-Princeton Township, inVentiv Health — Transforming Promising Ideas into Commercial Reality Job Title: Study Start-Up Specialist II Location: Princeton, NJ Job Description:
· Research local requirements for documentation of IRB / EC submission approvals, and subsequent follow-up documentation
· Liaise with study sites regarding essential document collection and, as required by country, site contract/ budget negotiatio … MORE INFO

Regulatory Associate Therapeutic

Monster.com

NJ-Plainsboro, Job Role: • Advise stakeholders of submission completion. • Find information and potential answers to challenging areas related to assigned projects in the interest of keeping the project streamlined and moving forward. • Assist in the preparation of regulatory documents. • Compile applications and prepare for sign-off (INDs/NDAs/BLAs/510Ks, IND amendments and Annual Progress Reports, NDA annual R … MORE INFO

Principal Biostatistician

Monster.com

NJ-East Windsor, PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed sig … MORE INFO

QA Compliance Specialist

Monster.com

PA-Frazer, Position Summary: This is a position requiring use and application of basic principles and concepts to suggest solutions to daily problems and perform routine work in conjunction with a supervisor. Substantial independence needs to be demonstrated, as do good record keeping, attention to detail, scheduling, and inventory skills. The incumbent will ensure compliance with GMP for Phase I-III interme … MORE INFO

Controlled Substance Specialist

Monster.com

NJ-Cranbury, JOB OVERVIEW: Experis Engineering currently has an immediate need for a Controlled Substance Specialist for one of our great pharma clients for a contract opportunity in NJ. Local candidates are strongly preferred. This person is taking an active role in all controlled substance transactions in Access and will play a major role in end of year DEA controlled substance destruction activities and the … MORE INFO

Pharmaceutical Formulations - Dry Powder - Aerosols

Monster.com

NJ-Dayton, We have an opening for a formulations chemist, Pharmaceutical Formulations - Dry Powder - Aerosols in the Dayton, NJ Area. Responsibilities for Formulations Scientist - Dry Powder - Aerosols • Blend dry powder formulations, operation / assembly / cleaning of mixing equipment, transferring of formulations from one type of container to another, conditioning experiments / working with analytical supp … MORE INFO

Senior Clinical Data Manager

Monster.com

PA-West Chester, Senior Clinical Data Manager Requirements: - BS Life Sciences or Computer Science - 5-7 years of data management experience in a clinical research setting - Strong working knowledge and prior experience directly managing/overseeing service providers and CRO’s is required - Prior experience managing clinical data for multiple studies at one time - Experience with computerized clinical data manageme … MORE INFO

Drug Patient Safety – Data Analyst

Monster.com

DE-Wilmington, Responsibilities: Excellent employment opportunity for a Drug/Patient Safety — Data Analyst in the Wilmington, DE area. Ensure compliance with global and local procedural documents and local implementation of Patient Safety objectives, policies, processes and procedures Review safety data output for accuracy and completeness prior to submission to internal and external sources Provide support to P … MORE INFO

Shown below: Philadelphia clinical research area jobs provided by Indeed job search

Clinical Research Associate (CRA)-ECD-10K sign on bonus!

Covance – Philadelphia, PA – Indeed.com

The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH. . . … MORE INFO

CLINICAL RESEARCH COORDINATOR C

University of Pennsylvania – Philadelphia, PA – Indeed.com

Proficient knowledge in GCP and human research protections regulations is desired. The ideal candidate would have at minimum 4 years of clinical research. . . … MORE INFO

Research Administrator

Temple University – Philadelphia, PA – Indeed.com

An equivalent combination of education and experience may be considered. Demonstrated knowledge of standard operating procedures and clinical research. . . … MORE INFO

Clinical Research Coordinator II - Dept of Medicine - Cardiology

Thomas Jefferson University and Hospitals – Philadelphia, PA – Indeed.com

Under the leadership team of the Jefferson Coordinating Center for Clinical Research, the Clinical Research Coordinator II work on a portfolio of clinical. . . … MORE INFO

CLINICAL RESEARCH COORD A

University of Pennsylvania – Philadelphia, PA – Indeed.com

Bachelor’s degree and at least 1 year of experience, preferably in clinical research, or an equivalent combination of education and experience is required. . . . … MORE INFO

RESEARCH COORDINATOR

University of Pennsylvania – Philadelphia, PA – Indeed.com

The minimum of a Bachelor’s degree and 1 to 2 years of experience or an equivalent combination of education and experience is required. . . . … MORE INFO

CLINICAL RESEARCH COORD II

Children's Hospital Philadelphia – Philadelphia, PA – Indeed.com

Must be knowledgeable on and have full understanding of good clinical practices (GCP) and regulatory responsibilities and will be held accountable for adherence. . . … MORE INFO

Clinical Research Associate

DOCS – Philadelphia, PA – Indeed.com

DOCS is actively recruiting for CRAs with Field Monitoring experience in the Philadelphia area for new opportunities. Experience with Oncology, Anti … MORE INFO

EndoVenous Clinical Specialist (Philadelphia)

Medtronic – Philadelphia, PA – Indeed.com

Bachelors Degree from accredited University or College, or Degree from an accredited Ultrasounds program, or equivalent experience. . . . … MORE INFO

Clinical Research Assistant I - Occupational Therapy/CRSRP

Thomas Jefferson University and Hospitals – Philadelphia, PA – Indeed.com

Thomas Jefferson University and Hospitals provide excellent clinical and compassionate care for our patients in the Philadelphia region, educate the health. . . … MORE INFO

Clinical Research Specialist - Kimmel Cancer Center - Full Time

Thomas Jefferson University and Hospitals – Philadelphia, PA – Indeed.com

BS/BA with 1-2 years clinical research experience or the equivalent. Should have 1-2 years prior experience in clinical research and/or regulatory work in the. . . … MORE INFO

SR RESEARCH ASSISTANT

Children's Hospital Philadelphia – Philadelphia, PA – Indeed.com

To learn more about the CHOP Research Institute and the research programs visit: . The Children’s Hospital of Philadelphia Research Institute is an. . . … MORE INFO

Clinical Trial Assistant North Wales PA

ICON Clinical Research – North Wales, PA – Indeed.com

Working closely with our global clinical teams the Clinical Trial and Project Managers to ensure the efficient and effective conduct of clinical trial studies. . . . … MORE INFO

Administrative Associate - Emergency Medicine

Thomas Jefferson University and Hospitals – Philadelphia, PA – Indeed.com

Thomas Jefferson University and Hospitals provide excellent clinical and compassionate care for our patients in the Philadelphia region, educate the health. . . … 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
6.2%
Year

Updated to reflect Oct 2014 unemployment rates

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