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Clinical Data Management
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Principal Statistical Programmer

Covance, Inc. a division of LabCorp® - Nationwide, 

Education/Qualifications Minimum Required: - BSc in a computing, life science, mathematical or Statistical subject. - A high computing content is considered beneficial; however proven computing skills are most important. - Alternative academic qualifications or experience are assessed to ensure equivalent background. Experience Minimum Required: - 8 years experience in provision...more

From Covance, Inc. a division of LabCorp® - 6/15/2018 5:48:18 AM

Sr Specialist MRL QA Technology

Merck & Co. - Rahway, NJ

Position Qualifications : Education Minimum Requirement: • B.A./B.S. in Computer Science, Information Systems or Science Required Experience and Skills: • Minimum of 3 years pharmaceutical or related industry experience, including work in IT/IS systems validation and/or GxP business quality Preferred Experience and Skills: • Knowledge of Good Clinical Practice and 21 CFR Part 11...more

From Merck & Co. - 6/14/2018 5:48:01 AM

Sr Assoc Drug Safety

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

Education/Qualifications - Non-degree + 5-6 yrs safety experience* - Associate degree + 4-5 yrs safety experience* - Associate degree RN + 4-5 yrs safety experience* - BS/BA + 3-4 yrs safety experience* - MS/MA + 2-3 yrs relevant experience** (1-2 yrs safety experience) - PharmD + 1-2 yrs relevant experience** (1 yr safety experience) - For PharmD, a one year resid...more

From Covance, Inc. a division of LabCorp® - 6/12/2018 5:44:32 AM

Sr Technical Project Manager

Merck & Co. - West Point, PA

Education: •B.A. or B.S. degree, preferably in life sciences, computer science, or related discipline. Required: •At least 6 years' experience in Clinical Data Management (or related discipline) for technology acquisition and implementation. At least 3 years' experience working with formal project management tools and processes. •In-depth knowledge of the clinical development process, p...more

From Merck & Co. - 6/12/2018 5:44:20 AM

Senior Specialist, IRT COA

Merck & Co. - Rahway, NJ

Education Minimum Requirement: • B.A. or B.S. degree, preferably in Life Sciences, Computer Science, Engineering or related discipline. Required Experience and Skills: • 6 years' experience in Clinical Data Management with at least 4 years' of IRT and/or COA working experience Preferred Experience and Skills: • Demonstrate knowledge of IRT & COA systems development processes • Knowled...more

From Merck & Co. - 6/7/2018 5:44:57 AM

Data Management Trial Manager

Merck & Co. - Rahway, NJ

Education Minimum Requirement: B.A. or B.S. degree, preferably in life sciences, computer science, or related discipline. Required Experience and Skills: • At least 3 years' of Clinical Data Management Experience; • Full life-cycle experience in clinical data management (data collection system development through database lock and close-out and submissions; • At least 1 year experience w...more

From Merck & Co. - 6/6/2018 5:48:50 AM

Data Scientist, Chemical Biology & Therapeutics

Novartis Pharmaceuticals - Cambridge, MA

Ph.D. or M.Sc. in a biology or computer science field, or related discipline, supported by a strong publication record • Demonstrated, strong communication skills, written and oral, and a successful track record of collaborating with cross-functional scientific teams • Fluency in SQL and R or Python is a prerequisite, and/or demonstrated Linux/Unix competency • Demonstrated working knowledge of...more

From Novartis Pharmaceuticals - 6/5/2018 5:42:06 AM

CDMA Project Lead (Ophthalmic/Vision Science and/or Contact Lens Exp)

Novartis Pharmaceuticals - Duluth, GA

• Bachelor's degree with 5 years of relevant experience OR HS Diploma w/13 years of relevant experience, Associate's degree w/ 9yrs years of relevant experience Master's degree w/2yrs years of relevant experience and PhD w/0 years of relevant experience. •Proficiency in the English required. •Minimum 5 years technical and operational experience in planning, executing, reporting and publishing...more

From Novartis Pharmaceuticals - 5/29/2018 5:46:41 AM

Electron Microscopy-Data Analysis Specialist (NCI)

Leidos Biomedical Research, Inc. - FREDERICK, MD

Qualifications: BASIC QUALIFICATIONS To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below: - Possession of a PhD degree from an accredited college or university according to the Council for Higher Education Accreditation in Biological Sciences, Structural Biology, or related discipline. (Additional qualifying experience may be substi...more

From Leidos Biomedical Research, Inc. - 5/23/2018 5:51:12 AM

The HireLifeScience.com Career Fair 2018

HireLifeScience.com - Edison, NJ

Required qualifications to attend: Attendance is free. Candidates must possess a 4 year life science related degree and 2 years professional experience working for a Life Science related company. An invitation to attend will be sent if the minimum qualifications are met. A general overview of job categories companies will be hiring for: -Research & Development -Clinical Research -Laboratory...more

From HireLifeScience.com - 5/22/2018 11:49:02 AM

Data Management Quality Leader

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Qualifications Essential •Education: Minimum of a BS in life sciences or computer science degree •Strong Data Management experience in the Biotech/Pharma/CRO industry (at least 5 years) •Strong Oncology Therapeutic Expertise (at least 3 years) •Demonstrated current understanding of GCP and regulatory requirements as they relate to data management systems and activities •Demonstrated curren...more

From AstraZeneca Pharmaceuticals - 5/22/2018 5:44:42 AM

CDMA Project Lead (Surgical, IOL Diagnostics Experience)

Novartis Pharmaceuticals - Fort Worth, TX

• Bachelors Degree plus 5 years technical and operational experience in planning, executing, reporting and publishing clinical studies (or equivalent combination of education and directly related work experience). • Ability to write, read and speak fluently in English. •. Experience in managing global multi-center clinical trials across multiple geographic regions. • Demonstrated ability to e...more

From Novartis Pharmaceuticals - 5/11/2018 5:31:45 AM

Senior Project Lead - CDMA (Surgical, IOL Diagnostics Experience)

Novartis Pharmaceuticals - Fort Worth, TX

• Bachelors Degree plus 7 years technical and operational experience in planning, executing, reporting and publishing clinical studies (or equivalent combination of education and directly related work experience). • Ability to write, read and speak fluently in English. •. Experience in managing global multi-center clinical trials across multiple geographic regions. • Demonstrated ability to ...more

From Novartis Pharmaceuticals - 5/11/2018 5:31:45 AM

Clinical Data Management Manager (NCI)

Leidos Biomedical Research, Inc. - ROCKVILLE, MD

Qualifications: BASIC QUALIFICATIONS To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below: - Possession of a Bachelor's degree in a related field from an accredited college/university according to the Council for Higher Education Accreditation (CHEA) (Additional qualifying experience may be substituted for the required education) For...more

From Leidos Biomedical Research, Inc. - 5/3/2018 5:51:07 AM

CDMA Project Lead

Novartis Pharmaceuticals - Duluth, GA

•Bachelors degree with 5 years relevant experience English •Minimum 5 years technical and operational experience in planning, executing, reporting and publishing clinical studies. •Well respected in eye care / research community •Demonstrated ability to establish strong scientific partnership with key external collaborators. •Proficient in MS Word, Excel, and PowerPoint •Thorough knowled...more

From Novartis Pharmaceuticals - 4/26/2018 5:47:19 AM

Principal Data Scientist

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

Education/Qualifications - PhD in computational, physical or life sciences with a strong quantitative focus, or BS/MS with equivalent experience. Experience - 8+ years of hands-on experience in the analysis, modeling, and visualization of large, complex, and heterogeneous data sets post BS (may include academic training). - Deep understanding and hands-on experience with statist...more

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

Clinical Data Manager Lead

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

Education/Qualifications - University/college degree (life science, pharmacy or related subject preferred), or certification - in a related allied health profession from an appropriately accredited institution (e.g., nursing ce11ification, medical or laboratory technology). - Additional relevant work experience will be considered in lieu of formal qualifications. - Broad knowledg...more

From Covance, Inc. a division of LabCorp® - 4/4/2018 5:55:42 AM

Sr. Medical Information Manager

AstraZeneca Pharmaceuticals - Wilmington, DE

Major Responsibilities General •Demonstrate scientific and business expertise relevant to therapeutic areas, including products, disease state management, emerging therapies, and the competitive landscape •Collaborate with key stakeholders to identify scientific information to meet customer needs •Monitor the medical environment (including medical inquiries) and apply scientific expert...more

From AstraZeneca Pharmaceuticals - 4/3/2018 5:47:14 AM

Protocol Coordinator (NCI)

Leidos Biomedical Research, Inc. - FREDERICK, 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, ...more

From Leidos Biomedical Research, Inc. - 3/30/2018 6:57:20 AM

Senior Statistical Programmer

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Major Responsibilities:  •Review a clinical study protocol with regard to statistical programming responsibilities •Review and provide input to a Statistical Analysis Plan (SAP) and Statistical Programming Plan (SPP) •Review and provide input to Case Report Forms (CRFs) and external data transfer agreements •Work cooperatively with study team members including but not limited to the bi...more

From AstraZeneca Pharmaceuticals - 3/22/2018 6:46:48 AM
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