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Phase II
Your career working on phase 2 clinical trials begins when you apply for jobs at HireLifeScience.com. We provide you with amazing opportunities, including clinical research assistant jobs, marketing positions, director jobs, and other great positions. By applying for a clinical research associate job through us, you’ll be able to work in a unique position, giving you the chance to build your resume and discover new life science positions. We work hard to make sure you can apply to jobs offered by some of the top life science and medical companies in the world!

When you click on a clinical research associate job, you’ll be taken to a page when you can learn more about the job description, the requirements, the company, and how you can apply. We have worked hard to make it easy for you to apply for positions as part of phase 2 clinical trials. Check out our great phase 2 clinical research assistant jobs we have featured today.

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QC Analyst - Microbiology (NCI)

Leidos Biomedical Research, Inc. - FREDERICK, MD

PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideration: - General knowledge of cGMP operations and BL2 - Analytical equipment qualification - Use of electronic systems - Demonstrated ability to interface with Manufacturing, Quality Assurance, Materials Management EXPECTED COMPETENCIES - Entry professional role, contributing i...more

From Leidos Biomedical Research, Inc. - 2/15/2018 5:47:06 AM

Clinical Trials Manager (NCI)

Leidos Biomedical Research, Inc. - FREDERICK, MD

PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideration: - Infectious disease and vaccine research experience - Knowledge of Quality Assurance/Quality Control processes - Knowledge of site selection activities and tracking site capabilities - Ability to read, speak, and write - Latin American Spanish and/or Brazilian Portuguese E...more

From Leidos Biomedical Research, Inc. - 2/15/2018 5:47:05 AM

Executive Medical Director, Cardiovascular

Novartis Pharmaceuticals - East Hanover, NJ

Minimum requirements Education: • An undergraduate degree with demonstrated clinical experience in the cardiovascular field, M.D. is a plus. • 8-10 years of pharmaceutical industry experience in medical affairs is required. • Strong academic background and Board Certification/Eligibility in Internal Medicine, or Cardiology is a plus. Experience/Professional Requirement: • Experience in mana...more

From Novartis Pharmaceuticals - 2/15/2018 5:46:31 AM

Statistical Research Associate (NCI)

Leidos Biomedical Research, Inc. - BETHESDA, MD

PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideration: - Experience working with high dimensional biomedical data (e.g., microarray, genomic, or immune assay data) - Knowledge of computing applications such as SAS/STAT and Python Leidos Overview: Leidos is a global science and technology solutions leader working to solve the world's t...more

From Leidos Biomedical Research, Inc. - 2/14/2018 5:43:08 AM

Clinical Research Associate (NCI)

Leidos Biomedical Research, Inc. - FREDERICK, MD

PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideration: - ACRP Certified CRA or SOCRA Certified Clinical Research Professional - Infectious diseases experience - Knowledge of an electronic Clinical Trials Management Systems - Knowledge of Department of Health and Human Service (DHHS) regulations - Experience developing Case Repo...more

From Leidos Biomedical Research, Inc. - 2/12/2018 5:45:51 AM

Clinical Research - Global Clinical Therapeutic Area Head, Cardiovascular & Metabolism

CSL Behring - King of Prussia, PA

Education & Experience: •Advanced degree (MD, PhD or PharmD) in life science/healthcare required. Board Certified (or non-USA equivalent) in Internal medicine or relevant sub-specialty highly preferred •Clinical development experience leading a therapeutic area or complex clinical program with a working knowledge of pharmaceutical and regulatory development processes is essential. •A min...more

From CSL Behring - 2/9/2018 5:54:16 AM

Senior Scientist, Downstream Biologics Process Development and Commercialization

Merck & Co. - West Point, PA

Education Minimum Requirement: • BS or MS in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry with 6 years (for BS) or 4 years (for MS) relevant experience. PhD candidates with 0+ year(s) of relevant experience will also be considered. Required: • Proven strong scientific, project, and people management skills • Strong communicator and ability to build bridges betw...more

From Merck & Co. - 2/9/2018 5:52:37 AM

Clinical Research Associate I

Covance, Inc. a division of LabCorp® - China, Shanghai Shi

Education/Qualifications - University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology). Experience In lieu of the above requirement, candidates with three or more years of relevant clinical research experience in pharmaceutical or CRO ...more

From Covance, Inc. a division of LabCorp® - 2/8/2018 5:46:09 AM

Associate / Medical Director / Lead Medical Director, Respiratory

Novartis Pharmaceuticals - East Hanover, NJ

Minimum requirements This position will be filled at a level commensurate with experience. Education: • MD or DO with 2-5+ years of pharmaceutical industry experience in Medical Affairs and/or Clinical Development. Board Certification/Eligibility in Internal Medicine, Allergy/Immunology, and/or Pulmonology is preferred. • PharmD or PhD with 2-5+ years of pharmaceutical industry experience in ...more

From Novartis Pharmaceuticals - 2/7/2018 5:45:38 AM

Protocol Coordinator (NCI)

Leidos Biomedical Research, Inc. - ROCKVILLE, MD

PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideratio n: - Knowledge of clinical data report preparation - Proficiency with Microsoft® software applications Leidos Overview: Leidos is a global science and technology solutions leader working to solve the world's toughest challenges in the defense, intelligence, homeland security, civil, and ...more

From Leidos Biomedical Research, Inc. - 2/6/2018 9:16:24 AM

Clinical Project Manager (NCI)

Leidos Biomedical Research, Inc. - FREDERICK, MD

PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideration : - Familiarity with Federal Acquisition Regulations (FAR) - Ability to speak, write, and understand Latin American Spanish and/or Brazilian Portuguese Expected Competencies: - Extensive knowledge of Food and Drug Administration (FDA) regulations and Good Clinical Practices (GCPs) -...more

From Leidos Biomedical Research, Inc. - 2/6/2018 9:16:24 AM

Protocol Coordinator (NCI)

Leidos Biomedical Research, Inc. - ROCKVILLE, MD

PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideration: - Knowledge of clinical data report preparation - Proficiency with Microsoft® software applications Leidos Overview: Leidos is a global science and technology solutions leader working to solve the world's toughest challenges in the defense, intelligence, homeland security, civil, and h...more

From Leidos Biomedical Research, Inc. - 2/6/2018 9:16:23 AM

Protocol Coordinator (NCI)

Leidos Biomedical Research, Inc. - ROCKVILLE, MD

PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideration: - Knowledge of clinical data report preparation - Proficiency with Microsoft® software applications Leidos Overview: Leidos is a global science and technology solutions leader working to solve the world's toughest challenges in the defense, intelligence, homeland security, civil, and h...more

From Leidos Biomedical Research, Inc. - 2/6/2018 9:16:23 AM

Global Program Regulatory Manager

Novartis Pharmaceuticals - East Hanover, NJ

Minimum requirements Science based BS or MS with requisite experience and demonstrated capability. Advanced degree (MD, Ph D, PharmD) preferred. Fluency in English as a business language. Additional language is an asset. Experience: Experience with regulatory submission and approval processes in 1 or more major regions. Experience in a global/matrix environment or cross-functional teams in the pha...more

From Novartis Pharmaceuticals - 2/6/2018 5:51:17 AM

Research Physician

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Qualifications •Medical Degree, with 5+ years of clinical experience •Board certification in a relevant clinical specialty, such as for instance nephrology, cardiology, endocrinology, internal medicine or other specialty Preferred Qualifications •Experience from clinical research, preferably with a PhD degree or equivalent, or a track record of scientific publications •Experience from ...more

From AstraZeneca Pharmaceuticals - 2/6/2018 5:51:01 AM

Assoc. Dir, Regulatory Affairs

Merck & Co. - Upper Gwynedd, PA

Education Requirement: Education Minimum Requirement: B.A. or B.S. degree Required Experience and Skills **: • Minimum 7 years' experience in pharmaceutical/biologics regulatory, legal, scientific, medical, or marketing disciplines • Direct experience with FDA regulations relating to advertising and promotion for prescription products AND / OR product development process, including labelin...more

From Merck & Co. - 2/2/2018 5:37:51 AM

Quality Engineer

Catalent Pharma Solutions - Madison, WI

The Role •Responsible for the execution of improvement projects as assigned by management •Serve as a lead for technical advice and perform multiple complex projects at a time •Maintain effective communication and positive working relationships with company management, internal departments and other sites to effectively implement and maintain Quality Operations •Should be able to propose de...more

From Catalent Pharma Solutions - 2/1/2018 5:46:57 AM

Clinical Scientist

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Major Responsibilities In collaboration with Study Team Physician(s) and Global Clinical Leader: •Organize and contribute to Program/Study clinical documents including (not inclusive) Investigator Brochures (IBs), Clinical Development Plans (CDPs), briefing documents, Protocol concept sheets and protocols (including amendments), Clinical Study Reports (CSRs), Pediatric Plans (ie PIPs/PSPs), ph...more

From AstraZeneca Pharmaceuticals - 1/31/2018 5:46:12 AM

Medical Affairs Leader/Senior Medical Affairs Leader

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Main Duties and Responsibilities: •As the Medical Affairs Leader/Senior Medical Affairs Leader, (INA) you will lead the development and execution of the Medical Strategy for SLE and other IFN disease.  The patient-centric approach is reinforced by science-led life cycle management programs and technologies. In this role, you will have global reach with a focus on Phase III through launch phase,...more

From AstraZeneca Pharmaceuticals - 1/29/2018 5:43:01 AM

Medical Affairs Leader/Senior Medical Affairs Leader – Gaithersburg, MD or Cambridge, UK

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Main Duties and Responsibilities: •As the Medical Affairs Leader/Senior Medical Affairs Leader, CVMD you will lead the development and execution of the Brand Integrated Medical Affairs Plan(s) so that relevant assets for the treatment of Chronic Kidney Disease (CKD) (1 or 2 brands within a defined remit) are developed in alignment with the Therapeutic Area (TA) Medical Strategy and executed to ...more

From AstraZeneca Pharmaceuticals - 1/29/2018 5:43:00 AM
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