41 Clinical Research job openings in the Philadelphia, Pennsylvania area

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Job listings, help wanted ads and employment postings (last updated on Monday, August 3)

Clinical Program Manager

Monster.com

PA-Plymouth Meeting, Clinical Program Manager Job Description: The Clinical Program Manager is responsible for management of clinical studies to support department objectives. Qualifications & Requirements: Required education: Bachelor/Master’s degree. At least 8 years of clinical trial management, clinical operations or clinical research and development experience including site monitoring. Experience in global proto … MORE INFO

Associate Manager/Manager, Site Relationships (G31/G32)(Philadelphia)

Monster.com

PA-Philadelphia, Associate Manager/Manager, Site Relationships Quintiles pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways … MORE INFO

Clinical Risk Management Associate

Monster.com

PA-Montgomery Township, Clinical Risk Management Associate Must have: -Both clinical and Pharmacovigilance experience. -Graduate (Masters) degree in nursing, health sciences, pharmacology, epidemiology, public health, or other relevant health-related field. - At least five years of experience in clinical, pharmacological, or related field of expertise. - Must have worked with patients in a medical or clinical setting as … MORE INFO

Clinical Research Associate / Project Coordinator

Monster.com

PA-Middle City West, Clinical Research Associate / Project Coordinator Clinical Research Associate / Project Coordinator Clinical Research Associate / Project Coordinator Clinical Research Associate / Project Coordinator Clinical Research - Center City Nonprofit! A Center City nonprofit is looking for a Clinical Research Associate! The research associate will oversee completion of trials from start to finish. Responsi … MORE INFO

UBC - Sr Pricing & Proposals Specialist - Pharma Commercial Services

Monster.com

PA-Blue Bell, SUMMARY OF POSITION The Pricing Analyst, Commercial Pharma Services position is responsible for developing pricing and proposals for client RFPs and any associated revisions for the following UBC services: Risk Management, Reimbursement and Nursing Support, and Patient Assistance Programs. The Senior Analyst will lead and coordinate the associated RFP response activities with sales, Senior Managem … MORE INFO

Clinical Data Coordinator

Monster.com

PA-Conshohocken, Requirements: Bachelor's degree 2-5 years of data review experience (reviewing listings, opened and closed queries) Rave EDC Data reviewing expertise Data query/resolution expertise Responsibilities: Clinical data review, query generation/resolution and reconciliation activities to support the delivery of clinical data to clients Review clinical trial data in accordance with Data Management Plans … MORE INFO

Statistician/SAS/Outcome Research,Pharmacovigilance,Hadoop,Drug Safety,CRA,Data Manager

Monster.com

NJ-Ewing, TechData is looking for Outcome research statistician(Econometrician, Economic Modeler), Biostatistician, Pharmacovigilance Physician Physician, Pharmacovigilance Scientist, SAS Programmer/Statistical Programmer (Some can be telecommuting), Hadoop Administrator, Sr. Clinical Data Manager, Drug Safety Specialist, Clinical Research Assoc IIIfor our pharmaceutical clients in Central NJ. Please see be … MORE INFO

Senior Contract Analyst (Clinical Trials)

Monster.com

PA-King of Prussia, Job Description The Senior Contract Analyst's primary role entails ensuring that data is extracted from Clinical Trial Agreements and uploaded accurately into the software to allow for payment to the intended parties that is reflective of the terms that were negotiated in the Clinical Trial Agreement. Responsibilities Review and interpret global clinical contract agreements, budgets and amendments … MORE INFO

DRUG SAFETY SPECIALIST

Monster.com

NJ-Princeton, Theradex ® is an international contract research organization providing complete professional services for the clinical research and development of pharmaceutical compounds, medical devices and diagnostic test in the areas of oncology and life-threatening diseases for over 30 years. Theradex ® conducts studies which lead to marketing approval of significant advances; and has built a reputation on as … MORE INFO

Scientist

Monster.com

NJ-Princeton, Scientist and Senior Scientist Seek Lc/ms/ms Scientists — NJ and Utah Seek Scientist with ELISA method development — MD, NJ Seek Project Manager Large Molecule / ELISA — MD, NJ Seek Project Manager Lc/ms/ms — NJ, NC, Utah Ask us for other job descriptions — Melissa@sageinc. net Research Scientist / Senior Research Scientist / Large Molecule — MD and NJ The major duties and responsibilities of a Res … MORE INFO

Laboratory Director - GLP

Monster.com

NJ-Princeton, Lab Director The Laboratory Director is responsible for the day to day operations of the biotechnology services laboratory located in NJ. This includes compliance, insuring that the clients are receiving scientifically sound results that meet or exceed GLP and CLIA requirement. The position is responsible for staffing the lab with the appropriate number of staff, including sample management, lab s … MORE INFO

Bioanalytical Project manager / Principal Investigator

Monster.com

NJ-Princeton, Project Manager / Principal Investigator Openings in NJ and Utah Requirements: The major duties and responsibilities include the following: 1. Managing bioanalytical projects which includes: 1. 1. Maintaining project schedule information (sample receipt, analyses required, data and report timelines, etc. ) 1. 2. Ensuring client contract and technical specifications are met. 1. 3. Performing duties of … MORE INFO

Sr. Scientist with PK and ADA

Monster.com

NJ-Princeton, Senior Research Scientist Seek Ph. D level Scientist with experience in method development with PK and anti-drug antibody ( ADA ) assays under GLP. Method development, method validation and sample analysis. for preclinical and biomarker characterization. Review data and documentation for SOP acceptance. Requirements: 3 years plus of method development and validation. Ph. D. ADA, PK development. Also … MORE INFO

Medical Director, Oncology Market Insights (Remote Position) Full-Time or Part-Time

Monster.com

NJ-princeton, What is Xcenda? Xcenda, a business unit of AmerisourceBergen Corporation, is an integrated, world-class health care consulting organization focused on value, reimbursement and patient access. For more than 2 decades, Xcenda has helped global biopharmaceutical companies as well as emerging early-phase firms successfully commercialize innovative medical treatments and technologies in complex and cos … MORE INFO

Clinical Research Associate

Monster.com

NJ-princeton, Clinical Research Associate (CRA) The compensation for this position is negotiable, we are not looking for entry level candidates this is a great FULL TIME opportunity within a growing organization. Offering full benefits and great pay! Please see below for the job description. EDUCATION AND/OR EXPERIENCE: A Bachelors' degree required (science-related discipline strongly preferred). A minimum of 3 … MORE INFO

CLINICAL DATA MANAGER

Monster.com

NJ-Princeton, Theradex ® is an international contract research organization with over 30 years of experience providing complete professional services for the clinical research and development of pharmaceutical compounds, medical devices and diagnostic tests in the areas of oncology and life-threatening diseases. Theradex ® conducts clinical trials towards the goal of marketing approval for new agents with the pot … MORE INFO

Clinical Documentation Reviewer

Monster.com

NJ-Princeton Township, Please reach out to the Recruiter, Corey Bond at cbond@apexsystemsinc. com Minimum Required: ¨Minimum 4 years' experience working in a clinical research environment. ¨Understanding of GCP and ICH guidelines. ¨Knowledge of Regulatory/Clinical document requirements. ¨Extensive experience working in clinical electronic systems. ¨Extensive knowledge of Microsoft Office products, web based applications, … MORE INFO

Registered Nurse (RN)

Monster.com

NJ-Plainsboro, Designation: ON- Site Reviewer Specialist Scope of work: Responsible for performing study activities regarding the management and verification of medical consistency checks (MCC), management of the requirements for reporting events for adjudication (EA), and surveillance of titration of patients within clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP … MORE INFO

Manager/Sr. Manager Clinical Pharmacology Global Regulatory Medical Writing

Monster.com

PA-West Chester, Overview The incumbent will be an experienced medical writer with specialization in clinical pharmacology. He/she will manage and oversee the preparation of clinical study protocols, clinical study reports, Investigator's Brochures, clinical pharmacology sections of US and EU clinical trial applications and marketing applications, and other high-level summary, briefing, and response documents in a … MORE INFO

Biostatistical Programmer

Monster.com

DE-Wilmington, Job Number: 430633 Biostatistical Programmer OVERVIEW Minimum Requirements: BA/BS degree Data Management experience and knowledge of CDISC standard are highly desirable Good SAS programming skills and attention to detail are essential Demonstrated knowledge of regulatory biostatistics, SOPs, and guidelines. Highly motivated and able to work well independently as well as being a good team player St … MORE INFO

Lead Biostatistical Programmer I/II/III

Monster.com

DE-Wilmington, Job Number: 430635 Lead Biostatistical Programmer I/II/III OVERVIEW Minimum Requirements: BA/BS degree MS degree is preferred for Levels II and III Data Management experience and knowledge of CDISC standard are highly desirable Good SAS programming skills and attention to detail are essential Demonstrated knowledge of regulatory biostatistics, SOPs, and guidelines. Highly motivated and able to wor … MORE INFO

Associate Director, Project Management

Monster.com

MultiLocation, Role: Provides leadership, mentoring, and support to the project management team to help meet overall business goals and objectives, while maintaining management responsibility for all personnel, revenue, profit, and contracts. Job Functions/Responsibilities: Manages a team of Senior Project Manager(s), Project Manager(s) and may be assigned additional supportive staff within the project managemen … MORE INFO

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

Clinical Research Associate- Philadelphia, PA Job

MSD – Philadelphia, PA – Indeed.com

Clinical Research Monitor(CRA). Clinical Research Associate- Philadelphia, PA-CLI004095. Clinical Research Associate, Oncology, Philadelphia, PA. . . . … MORE INFO

CLINICAL RESEARCH MONITOR

Fox Chase Cancer Centre – Philadelphia, PA – Indeed.com

5 Years experience as a Clinical Research Associate or Clinical Research Coordinator (Required). Ensures protocol compliance at the clinical research sites. . . . … MORE INFO

Clinical Research Coord II

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

Clinical Research Coordinator training. 2-3 years relevant research experience is required. Thomas Jefferson University and Hospitals provide excellent clinical. . . … MORE INFO

Clinical Research Assistant-Nutrition

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

Experience in pediatric clinical nutrition or clinical research is preferable. Ability to function with minimal supervision in a clinical research setting. . . . … MORE INFO

Research Program Specialist

Department of Veterans Affairs – Philadelphia, PA – Indeed.com

Performs professionally responsible research for a substantial portion of time, leads activities of the research team, or participates in the activities of the. . . … MORE INFO

REGULATORY COORDINATOR

Fox Chase Cancer Centre – Philadelphia, PA – Indeed.com

Two years experience in healthcare-related office environment, preferably in clinical research along with working knowledge of protocol development process and. . . … MORE INFO

Clinical Assistant

University of Pennsylvania Health System – Philadelphia, PA – Indeed.com

Clinical Assistant - Neurology. Penn Medicine employees are actively engaged and committed to our mission. The Clinical Assistant will demonstrate flexibility. . . … MORE INFO

Clinical Documentation Improve Specialist

Global Interworks Solution – Philadelphia, PA – Indeed.com

Required • Strong knowledge base of the conventions, rules and guidelines for multiple classification and reimbursement systems (i. e. . . . … MORE INFO

MANAGER, CLINICAL RESOURCE CTR

Temple University Health System – Philadelphia, PA – Indeed.com

Combination of relevant education and experience may be considered in lieu of degree. From nationally recognized physicians, sophisticated services and the most. . . … MORE INFO

CLINICAL RESEARCH ASSISTANT A

University of Pennsylvania – Philadelphia, PA – Indeed.com

A High School Diploma or GED and 1 year to 2 years of experience or equivalent combination of education and experience is required. . . . … MORE INFO

Experienced Clinical Research Associate

NewLink Genetics – Philadelphia, PA – Indeed.com

NewLink Genetics is looking for experienced Clinical Research Associates (CRA) to work on exciting oncology clinical trials. . . . … MORE INFO

CLINICAL RESEARCH COORD A

University of Pennsylvania – Philadelphia, PA – Indeed.com

The Clinical Research Coordinator A ( CRC A) will work closely with faculty and staff, particularly the Senior Research Coordinator, on clinical research. . . … MORE INFO

Clinical Data Analyst (Philadelphia, PA)

Cancer Treatment Centers of America – Philadelphia, PA – Indeed.com

Clinical Data Analyst. Three or more years of experience working with clinical departments (may include, R. N. , RPh, or other clinical exposure) in a hospital. . . … MORE INFO

Clinical Documentation Improvement Specialist - 6 Month Contract

SERJ Solutions – Philadelphia, PA – Indeed.com

RHIA, RHIT, CCS, CCS-P, CCD or CDIPRequired • Strong knowledge base of the conventions, rules and guidelines for multiple classification and reimbursement. . . … MORE INFO

Medical Writer|| J&J ||SPRING HOUSE ,PA

Radient Systems – Spring House, PA – Indeed.com

Identify and resolve, with the help of other functional areas, clinical and statistical issues in the interpretation of clinical data. Associate’s Degree -. . . … MORE INFO

Research Assistant

Temple University – Philadelphia, PA – Indeed.com

Under general supervision, the Research Assistant provides professional level research support requiring the application of standard research practices and. . . … MORE INFO

Associate Sr, Clinical Research

Intersect ENT – Philadelphia, PA – Indeed.com

Maintain the Clinical Trial Documentation system per clinical procedures and in compliance with GCP guidelines, FDA regulations and IRB requirements. . . . … MORE INFO

Pharmaceutical Drug Safety Associate

DOCS – Philadelphia, PA – Indeed.com

The successful candidate will have relevant clinical research/pharmaceutical industry experience, preferably in pharmacovigilance/drug safety, with knowledge of. . . … MORE INFO

Project Specialist

Bracket – Wayne, PA – Indeed.com

College degree (B. S. , B. A. )/University Degree for EU candidates or equivalent years of experience. Set up master systems, additional study hardware, study site. . . … 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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