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Clinical Research
The clinical research industry features a wide array of great positions for individuals who are interested in clinical research assistant jobs in the life science industry. HireLifeScience.com features a wide array of clinical research associate jobs, including data management, coordinator, and drug safety clinical research associate job options. We have dozens of job opportunities available in these fields, allowing you to find the ideal position or apply for your first life science job out of college. When you come to HireLifeScience.com to search for a clinical research associate job or any of the other positions in the clinical research field, you can feel confident that we give you all the information you need before applying for the position. All you have to do is click on of these clinical research associate jobs, read the description, and then apply. Whether you are interested in clinical research assistant jobs in the US or outside of the country, we have amazing options for you.
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Director, Clinical Safety Physician

CSL Behring - King of Prussia, PA

Education: Physician (MD or equivalent) Experience: Minimum of 2 experience required, preferred 5 years pharmacovigilance and / or clinical research / clinical safety experience in the pharmaceutical environment (industry, CRO). Medical practice of at least 2 years, preferred is a specialization in a relevant medical area including medical practice. Competencies: • Sound clinica...more

From CSL Behring - 4/20/2018 5:53:43 AM

Physician Assistant (NCI)

Leidos Biomedical Research, Inc. - BETHESDA, MD

PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideration: - Bone marrow experience 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 health markets. The company's 33,000 employees support vital missions for gover...more

From Leidos Biomedical Research, Inc. - 4/20/2018 5:52:12 AM

Clinical Project Administrator

Covance, Inc. a division of LabCorp® - Japan, Tokyo-to

Education/Qualifications - Diploma or equivalent - Minimum one (1) year administrative experience or equivalent training - Strong verbal and written skills - Attention to details Experience - Basic knowledge related to clinical development such as Good Clinical Practice - Basic knowledge of pharmaceuticals and medical devices law.

From Covance, Inc. a division of LabCorp® - 4/20/2018 5:50:53 AM

Senior Administrative Assistant, Global Clinical Trial Organization

Merck & Co. - Montreal (Kirkland), CA

Required: • High School Diploma, a DEC in Office Technology or its equivalent would be an asset • More than five years of relevant experience • Advanced knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook) is essential. • Knowledge of SAP/COMET • Language: Bilingual (French and English), written and oral Preferred: • Experience processing Corporate Cred...more

From Merck & Co. - 4/20/2018 5:50:42 AM

Clinical Project Manager/Senior Clinical Project Manager

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Requirements/Qualifications: Education : •University degree, preferably in a biologic/scientific discipline Experience : o   5 + years of biotech and/or pharmaceutical industry experience Special Skills/Abilities : •Thorough understanding of country level regulations, ICH and GCP guidelines •Thorough understanding of cross-functional clinical processes including data management, biosta...more

From AstraZeneca Pharmaceuticals - 4/20/2018 5:50:18 AM

Biometrics Clinical Study Planning Manager – Permanent

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Main Duties and Responsibilities Reporting to the Pipeline & Delivery Lead you will act as the Project Manager for assigned clinical projects, partnering with the B&I teams to ensure they deliver to plan.  This will be done by: •Partnering with Biometrics Team Leaders (BTL's); Programming Team Leaders (PTL's) and alliance directors to develop study level delivery plans •Forecasting resource n...more

From AstraZeneca Pharmaceuticals - 4/20/2018 5:50:18 AM

Clinical Scientist, Clinical Research

Amicus Therapeutics - Cranbury, NJ

Roles and Responsibilities - Build and maintain a good knowledge of the existing data for our products, competitor products, and the literature about the disease. - Support Clinical Research physicians in the development of essential documents such as protocols and protocol amendments, conduct literature reviews, and assist in data evaluation and interpretation. Developing slides for team pres...more

From Amicus Therapeutics - 4/19/2018 12:59:21 PM

Clinical Trials Manager

Amicus Therapeutics - Cranbury, NJ

Roles and Responsibilities - Manages clinical studies, including vendor management and oversight including CROs, IRB, DSMB. - Organize and participate in investigational meetings and site training. - Coach and mentor all staff under him/her; set objectives, solicit 360° feedback from stakeholders and conduct performance reviews to foster growth of staff. - Ensure all necessary training...more

From Amicus Therapeutics - 4/19/2018 12:59:21 PM

Executive Director, Global Head of Safety and Pharmacovigilance

Amicus Therapeutics - Cranbury, NJ

Roles and Responsibilities - Lead the Global Drug Safety and Pharmacovigilance function - Have direct managerial responsibilities pertaining to the function as appropriate - Be responsible for oversight of global drug safety processes and drug safety deliverables - Build on the existing Drug Safety and Pharmacovigilance function at Amicus. - Provide detailed, accurate and timely medical...more

From Amicus Therapeutics - 4/19/2018 12:59:21 PM

Sr. Director, Biostatistics and Data Management

Amicus Therapeutics - Cranbury, NJ

Roles and Responsibilities - Contributing to the development of study protocols, in particular, the statistically-related sections (e.g. sample size calculations, statistical methodology, and statistical analyses). - Identifying the most appropriate analytical models/methods for clinical studies, and conducting research on statistical methodology, as needed, to accomplish this. - Developing ...more

From Amicus Therapeutics - 4/19/2018 12:59:21 PM

Associate Director, Clinical Research

Amicus Therapeutics - Cranbury, NJ

Roles and Responsibilities - Develop, author and execute on study protocols and amendments by investigating the literature, searching databases and other existing/investigational products, working with key opinion leaders, clinical trial investigators, and internal scientific, pharmacology and regulatory teams. - Review the data generated during the execution of a study to gather a medical und...more

From Amicus Therapeutics - 4/19/2018 12:59:20 PM

Quality Control Specialist (NCI)

Leidos Biomedical Research, Inc. - BETHESDA, MD

PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideration: - Analytical assay experience - Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211) Leidos Overview: Leidos is a global science and technology solutions leader working to solve the world's toughest challenges in the defense, intelligence, home...more

From Leidos Biomedical Research, Inc. - 4/19/2018 5:44:48 AM

Manufacturing/Cell Therapy Specialist (NCI)

Leidos Biomedical Research, Inc. - BETHESDA, MD

PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideration: - Vector production and/or cell therapy products experience - Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211) Leidos Overview: Leidos is a global science and technology solutions leader working to solve the world's toughest challenges in t...more

From Leidos Biomedical Research, Inc. - 4/19/2018 5:44:48 AM

External Lab Mgr

Covance, Inc. a division of LabCorp® - Indianapolis, IN

Education/Qualifications Bachelors degree or equivalent education. Prefer a Masters degree in MT/MLT. Experience Minimum Required: - Experience in change management and influencing without authority. - Demonstrated expertise in leading change. - 2 years of clinical trial management, vendor management, or client relationship management experience. - Experience as a genomics t...more

From Covance, Inc. a division of LabCorp® - 4/19/2018 5:44:31 AM

Associate Director/Director Clinical Development-Nephrology

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Requirements/Qualifications: Education : •MD required with a current medical license preferred. •Medical specialty and sub-specialty training and certification (or eligibility) are highly desirable in Nephrology. Experience :  •Clinical or research experience (in an academic, pharmaceutical or CRO environment) related to the design and/or conduct of clinical studies in Nephrology...more

From AstraZeneca Pharmaceuticals - 4/19/2018 5:44:04 AM

Principal Scientist, Clinical Research and Process Development

Novartis Pharmaceuticals - East Hanover, NJ

Education:BS/Masters/PhD in Immunology, Cell Biology, Immunotherapy, Cell/Gene Therapy or equivalent. Languages: Good knowledge of English (oral and written). Experience/Professional requirement: Bachelor degree with 8+ years of industry experience OR Master degree with 5+ years of industry experience OR a PhD with 3+ years relevant experience in Immunology/Cell Therapy • Scientific background an...more

From Novartis Pharmaceuticals - 4/19/2018 5:43:44 AM

Study Dir II Tox

Covance, Inc. a division of LabCorp® - Madison, WI

Education/Qualifications - PhD in toxicology or related subject, DVM or equivalent degree. Experience may be substituted for education. Experience - Zero to two years of related experience. Skilled in performing scientific presentations and preparing scientific publications

From Covance, Inc. a division of LabCorp® - 4/18/2018 5:47:57 AM

Associate Project Manager, Oncology

Covance, Inc. a division of LabCorp® - Princeton, NJ

Education/Qualifications Required: - University/college degree (life science preferred), or certification in a related allied health profession(i.e. nursing, medical or laboratory technology) from an appropriately accredited institution. - In lieu of the above requirement, candidates with five (5) or more years of relevant clinical research experience in pharmaceutical, CRO industries or ...more

From Covance, Inc. a division of LabCorp® - 4/18/2018 5:47:57 AM

Diabetes Care Specialist Brookhaven Mississippi Job

Novo Nordisk Inc. - Brookhaven, MS

Business Manager, Clinical Research, Diabetes, Healthcare, Management, Medical, Medical Research, Special Medicine

From Novo Nordisk Inc. - 4/18/2018 1:27:23 AM

Diabetes Care Specialist San Diego South California Job

Novo Nordisk Inc. - San Diego, CA

Business Manager, Clinical Research, Diabetes, Healthcare, Management, Medical, Medical Research, Special Medicine

From Novo Nordisk Inc. - 4/18/2018 1:27:23 AM
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