32 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, August 28)

Associate Director, Regulatory Affairs - Steriles

Monster.com

PA-Horsham, Overview This position is responsible for the supervision/preparation and critical review of high quality regulatory submissions to the FDA including ANDAs, NDAs, amendments, supplements and annual reports. The Associate Director evaluates complex regulatory issues and provides accurate and timely recommendations and alternatives, as needed, to the Director. The Associate Director will establish r … MORE INFO

Clinical Research Protocol Analyst

Monster.com

PA-Horsham, Role: The primary role of the Clinical Research Protocol Analyst will be to review RFP material (protocol and related documents), appraise new and current business opportunities to include proposal planning, recruitment strategy development and operational implementation. Individuals must demonstrate a comprehensive understanding of clinical research patient recruitment across multiple therapeutic … MORE INFO

CRA / Senior CRA - Nationwide Home Based Positions

Monster.com

PA-Philadelphia, Worldwide Clinical Trials is a therapeutically focused global CRO that provides full-service drug development services to the pharmaceutical and biotechnology industries. As one of the most innovative and scientifically-driven contract research organizations, we offer exceptionally strong clinical trial methodology integrated with an effective global operations network. We are currently seeking hi … MORE INFO

Senior Manager, Site Activation

Monster.com

PA-North Wales, Sr. Manager Site Activation The site activation manger is responsible for ensuring the successful and timely activation and maintenance of investigative sites to ensure that sites are activated in line with the study timelines and client expectation. This role can be filled anywhere in the U. S. or E. U. Overview of the Role Recognize, exemplify and adhere to ICON's values which center around our co … 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 Data Coordinator

Monster.com

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

Senior Medical Writer - Office or Home Based

Monster.com

PA-King of Prussia, Worldwide Clinical Trials (WCT) is a leading therapeutically focused Contract Research Organization (CRO) that applies deep therapeutic expertise to help customers achieve their drug development goals. WCT’s global footprint, full complement of development service offerings, and innovative use of proprietary and cutting edge technology, bring about an environment which allows us to focus on identi … 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

Clinical Data Coordinator

Monster.com

NJ-Princeton, Requirements: Bachelor's degree preferred 2-5 years of data review experience (reviewing listings, opened and closed queries) EDC experience in Rave or Inform only Data reviewing expertise Data query/resolution expertise. Responsibilities: Clinical data review, query generation/resolutions and reconciliation activities to support the delivery of clinical data to clients Review clinical trial data … MORE INFO

Clinical Supply Project Assistant

Monster.com

NJ-Montgomery, Title : Clinical Supply Project Assistant Required skills : BS in science or engineer 3-5 years exp working in Clinical Supplies or 10 years of commensurate exp Knowledge of GMPs Clinical Supplies preparations and procedures Excellent written , verbal, organization and planning skills Responsibilities : Plan for, coordinate, and oversee preparation of labeling and secondary packaging of supplies f … MORE INFO

Post-Doc Research Associate-Large Molecules-BAS

Monster.com

NJ-Plainsboro, Xenobiotic Laboratories (XBL), a subsidiary of the Lab Testing Division of WuXi AppTec, Inc. , is a leading contract research laboratory specializing in small & large molecule Bioanalytical, drug metabolism, and pharmacokinetic services to the pharmaceutical, animal health and agrochemical industries. XBL is seeking a Post Doc Research Associate (Large Molecules for our Bioanalytical Department). E … MORE INFO

Senior Medical Writer

Monster.com

PA-Exton, Our client is a reputable pharmaceutical company seeking a Senior Medical Writer with Oncology experience who is able to be ON-SITE in Exton, PA (with ability to work from home 1 day per week). This is a 6 month contract position with potential to go permanent! If interested, please apply ASAP to speak to a recruiter for more information! Requirements: BS degree; Advanced degree in a relevant scie … MORE INFO

Director Medical Affairs - Oncology Compendia Information

Monster.com

NJ-New Brunswick, Oversee team that provides patients, healthcare providers and payers with practical and clinically relevant information related to oncology therapeutics.
· Implement publication plans.
· Support Key Opinion Leader engagement activities.
· Plan and participate in advisory board activities.
· Maintaining relationships with key scientific organizations and support the planning of clinical trials.
· S … MORE INFO

Shown below: jobs by Juju.com

Clinical Research Associate

DOCS – Philadelphia, PA – Climber

…
· Minimum of 3 years of independent monitoring experience
· Must be detail oriented
· Experience with device trials (endovascular preferred but not required) Candidates … MORE INFO

Home-Based Clinical Study Manager

DOCS – Philadelphia, PA – Climber

…of Expert Advisory Panels within programs.
· Responsible for management/oversight of clinical monitoring of research studies, which includes production and approval … MORE INFO

Global Trial Manager

DOCS – Philadelphia, PA – Climber

… trial experience in the pharmaceutical industry or CRO. Requires clinical research operational knowledge, project planning/management and communication skills, … MORE INFO

Site Manager-Northeast

DOCS – Philadelphia, PA – Climber

…contingency planning and implementation in partnership with other functional areas to achieve clinical research target. Ensures site study supplies (such as Non-IP, … MORE INFO

Biostatistician - home-based

DOCS – Philadelphia, PA – Climber

…years of post-graduate statistical experience in the pharmaceutical industry or medical research Or
· Doctoral degree in Statistics/Biostatistics or other subject with … MORE INFO

Clinical Research Scientist

Clinical Solutions Group – King Of Prussia, PA – Climber

Clinical Research Scientist: Responsibilities will include, but are not limited to, the following:
· Assist the Clinical Research Physician to interface with … MORE INFO

Statistical Programmer (Oncology)

Personify – Upper Darby, PA – Climber

…with both programming datasets and QC Analysis. - In-depth knowledge of applicable clinical research regulatory requirements; ie, Good Clinical Practice (GCP) … MORE INFO

Early Candidate Clinical Lead, Hematology

Pfizer Inc. – , PA – beyond.com

…and driver of strategic technical alignment between the Global Medical Development and Research Unit clinical triads.
· Ensures that POC study designs, transition … MORE INFO

Director, Clinician MD Hematology

Pfizer Inc. – , PA – beyond.com

…therapeutic area, Rare Diseases and/or Hematology; three to five years in clinical research with in the pharmaceutical and/or healthcare industry.
· Practical … MORE INFO

Sr. Director Global Medical Affairs Lead, Palbociclib

Pfizer Inc. – , PA – beyond.com

…The Sr. Dir GMAL will take a leadership role in the design and development of Clinical Research Collaborations (CRCs) and Phase IV studies in order to facilitate … MORE INFO

Clinical Study Associate

Clinical Solutions Group – Collegeville, PA – Climber

…knowledge of Good Clinical Practice (GCP) and other regulations governing clinical research . . Demonstrates some drug development experience within the … MORE INFO

Senior Statistical Programmer

Personify – Ridley Park, PA – Climber

…with both programming datasets and QC Analysis. - In-depth knowledge of applicable clinical research regulatory requirements; ie, Good Clinical Practice (GCP) … MORE INFO

AD of Clinical Data Management

Personify – West Chester, PA – Climber

…multiple ongoing tasks, and understand the differing priorities. - Proven experience in clinical research with a strong knowledge of SOPs and accepted practices. … MORE INFO

Corporate Counsel

Pfizer Inc. – , PA – beyond.com

…Governance activities Responsible for support of US marketing, sales, medical and clinical research support, including:
· Advertising and promotion and all product … MORE INFO

Sr. Director, Global Clinical Leader, Rare Diseases, Renal

Pfizer Inc. – , PA – beyond.com

…and mission of making the world a healthier place. Role Description The Global Clinical Lead in the RDRO (Rare Diseases, Renal, Other) Therapeutic Area represents … MORE INFO

Lead Senior Statistical Programmer

Personify – Norristown, PA – Climber

…both programming datasets and QC Analysis. - In-depth knowledge of applicable clinical research regulatory requirements. - Knowledge of statistics, programming … MORE INFO

Medical Director, CNS

Personify – North Wales, PA – Climber

…Certification in Neurology or Psychiatry is required and a minimum two years' Clinical Research experience within Academia or the Pharmaceutical, Biotech or CRO … MORE INFO

Medical Director, Medical Device

Personify – North Wales, PA – Climber

…in Internal Medicine or other therapeutic area is required.
· Minimum two years' Clinical Research experience with medical devices within the Pharmaceutical, Biotech … MORE INFO

Trial Manager Nationwide

DOCS – North Wales, PA – Climber

… Trial Managers. We are seeking candidates with a minimum of 5 years of clinical research experience having worked in either a CRO or Pharma environment. Local … 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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