| |
|
|
 |
|
|
|
|
| Jobs in biotechnology,
pharmaceutical, medical devices and life sciences
industries. |
|
|
|
|
|
|
|
|
 |
| |
|
|
|
|
|
management |
|
|
|
|
|
Education: |
|
Position type: |
Full Time Employee |
Experience: |
|
|
|
Area(s) of expertise desired: |
Administration
|
|
|
Description: |
|
kidjirourirhujfririeioeikjfufiriiodjkdjfdidikdjkifjfjfjfjfjfncnvbvnvmkdksowowowieuryrjfjfjhfhjdmxnxbcbcbvnmxkwkwiwi
|
|
|
Requirements: |
|
iwiuejhhfgfhjdksowowieiruryuyhfhfjdfncnvnbvncmckxkswowiuruyruyrudjdjfhfghfjdkdkwowowowieuiruruhfjfjfdjdjd
|
|
|
|
|
| |
|
|
Clinical Project Manager |
|
|
|
Category: |
Clinical Research- Pharma-Biotech
|
|
|
Education: |
Bachelors |
Position type: |
Full Time Manager |
Experience: |
3 years |
|
|
Area(s) of expertise desired: |
Business Development, Clinical Research, Project Management
|
|
|
Description: |
To manage clinical studies
To ensure that studies are performed and completed in accordance with the pre-defined budget, timelines and quality specifications
To ensure that a safety reporting system is in place and that safety reports are provided to the Safety Department in a time manner
To ensure that studies are conducted in accordance with GCP requirements and relevant company SOPs
Main contact with Local Regualtory Authorities.
|
|
|
Requirements: |
Bachelor's degree in a health care or other scientific equivalent;
Experience working on clinical trials for at least 3 years;
In depth knowledge of applicable clinical research requirements;
Strong written and verbal communication skills including good command of English language;
Computer skills including Microsoft Word, Excel and PowerPoint;
Excellent communication, organizational and problem-solving skills;
Effective mentoring, communication and training skills.
|
|
|
|
|
| |
|
|
CLINICAL TEAM LEAD |
|
|
|
Category: |
Clinical Research
|
|
|
Education: |
|
Position type: |
Full Time Employee |
Experience: |
3 years |
|
|
Area(s) of expertise desired: |
Clinical Research
|
|
|
Description: |
An excellent opportunity has arisen to join this global Contract Research Organisation as a Clinical Team Lead.
The purpose of the role is to manage the execution of the clinical component of study protocols in accordance with the scope of work and contracted timelines.
May act as a CTL for large scale projects under the supervision of a more senior CU, or Line Manager. May also serve as a Sr Clinical Research Associate (Sr CRA) within the project or other projects as needed.
ALL APPLICATIONS TO BE MADE IN ENGLISH PLEASE.
|
|
|
Requirements: |
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines
In depth therapeutic and protocol knowledge as provided in company training
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer
Strong written and verbal communication skills including good command of English language
Excellent organizational and problem-solving skills
Effective time management skills
Strong presentation skills
Effective mentoring and training skills
Ability to lead and motivate a culturally-mixed clinical team
Ability to manage competing priorities
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Bachelor’s degree in a health care or other scientific discipline or educational equivalent; 3 years clinical monitoring and one year in a project leadership role or equivalent combination of education, training and experience
|
|
|
|
|
| |
|
|
CLINICAL RESEARCH ASSOCIATES (all levels) |
|
|
|
Category: |
Clinical Research
|
|
|
Education: |
|
Position type: |
Full Time Employee |
Experience: |
1 year |
|
|
Area(s) of expertise desired: |
|
|
|
Description: |
Our client, a highly reputable leading global Contract Research Organisation, is looking for Clinical Research Associates to join the team. The purpose of the role is to identify, select, initiate and close-out appropriate investigational sites for clinical studies and to monitor these sites ensuring that the studies are performed in accordance with the SOPs, applicable regulations and ICH-GCP guidelines.
ALL APPLICATIONS TO BE MADE IN ENGLISH PLEASE.
|
|
|
Requirements: |
Education and qualifications
Medical/science background and 1 year previous clinical research experience;
Ability and willingness to travel at least 50% of the time;
Ability to review and evaluate clinical data;
Computer literacy desirable;
Good use of English;
Good oral and written communication skills.
|
|
|
|
|
| |
|
|
Biotechnology and Public Health |
|
|
|
|
|
Education: |
Doctorate |
Position type: |
Full Time Manager |
Experience: |
3 years |
|
|
Area(s) of expertise desired: |
Biochemistry, Clinical Research, Microbiology, Professional Services, Quality Control
|
|
|
Description: |
A three-year fellowship position will be available at the Center for Drug Evaluation and Research, FDA after January 2008. This position is ideal for recent graduates with a background in Chemical Engineering, Microbiology, Virology, Biochemical Engineering, Molecular Biology, or a related field and a strong interest in the intersection of the public health and the biotechnology industry. The primary responsibilities of the position are 1) conduct a survey of current practices (bench marking) for biotechnology manufacturing unit operations to identify the key benefits and gaps in their viral clearance capacity and 2) design and conduct lab-based projects that address the most urgent gaps in viral clearance by the identified unit operations. The individual will work as part a collaborative project between CDER and Eli Lilly, Inc. The project represents an excellent opportunity for individuals to impact the direction of their research career and gain experience in an area of high industry relevance. Considerable organizational skills and the ability to work in a team are required.
For a recent basic science graduate interested in breaking into the biotechnology arena, this is a rare opportunity to work with emerging technology in the leading biotechnology regulatory agency in collaboration with a leading biotechnology firm. The position ranges from GS-9 (~$40,000/yr) to GS-11 (~$48,000/yr) equivalent depending on qualifications. A doctoral degree in Chemical Engineering, Microbiology, Virology, Biochemical Engineering, Molecular Biology, or a related field is preferred. This position requires U.S. citizenship or permanent resident status. For consideration, candidates should submit their resumes prior to Feb 15, 2008.
|
|
|
Requirements: |
|
A doctoral degree in Chemical Engineering, Microbiology, Virology, Biochemical Engineering, Molecular Biology, or a related field is preferred. This position requires U.S. citizenship or permanent resident status.
|
|
|
|
|
| |
|
|
nurse |
|
|
|
|
|
Education: |
|
Position type: |
Full Time |
Experience: |
|
|
|
Area(s) of expertise desired: |
|
|
|
Description: |
|
|
|
Requirements: |
|
|
|
|
|
| |
|
|
Process Engineering Associate on a Contract basis. |
|
|
|
Category: |
Biotechnology, Pharmaceiuticals
|
|
|
Education: |
|
Position type: |
Full Time Employee |
Experience: |
9 years |
|
|
Area(s) of expertise desired: |
Chemical Engineering
|
|
|
Description: |
|
The position requires representing clients in bio and pharmaceutical industry in their capital projects. This translates into preparation and review of typical project deliverables, coordination between major project disciplines, operations, process development, QA, EHS, vendors/suppliers. Firm knowledge of Pharmaceutical and Biotech processes from design and operability perspective is a must.
|
|
|
Requirements: |
|
Degreed Process Engineer with 8 to 10 years of experience in pharmaceutical, biotech process design. Established knowlegde of biopharm project execution. Proven ability to generate and review process, mechanical, instrument and control deliverables. Good technical writing capability.
|
|
|
|
|
| |
|
|
Clinical Research Associate/Senior Clinical research associate- office/home based |
|
|
|
Category: |
QA - Quality Control, Biotechnology, Engineering, Chemistry, Life Sciences, Clinical Research, Clerical/Administrative, Management/Executive, Medical Management, Pharmacy/Pharmacology, Medical Equipment, Regulatory Affairs, Healthcare, Sales/Marketing, IT/Hardware/Software
|
|
|
Education: |
|
Position type: |
Full Time Employee |
Experience: |
2 years |
|
|
Area(s) of expertise desired: |
Clinical Research
|
|
|
Description: |
JOB FUNCTIONS/RESPONSIBILITIES:
Recruitment of investigators.
Co-ordinate all the necessary activities required to set up and monitor a study, including the following:
Identify investigators
Help, when requested, in preparation of regulatory submissions
Design patient information sheets and consent forms.
Ensure timely submission of protocol/consent documents for ethics/IRB approval.
Placement and initiation visits.
Conduct regular monitoring visits in accordance with site monitoring SOP / Sponsor site monitoring SOP, as appropriate
Maintain all files and documentation pertaining to studies.
Motivate investigators in order to achieve recruitment targets.
Complete accurate study status reports.
Ensure the correct storage of drugs and the diligent account of all drugs in accordance with SOPs.
Keep the project manager informed.
Process case record forms to the required quality standards and timelines.
Deal with Sponsor generated queries in a timely manner.
Ensure the satisfactory close-out of investigator sites.
Participate, if requested, in the preparation of and review of study documentation, e.g. draft protocols, draft CRFs, monitoring guidelines and elements of final report.
Ensure correct archiving of files on completion of a study.
Co-operate with sponsor and/or QA personnel in the conduct of QA audits.
Maintain patient and sponsor confidentiality.
|
|
|
Requirements: |
Cost effectiveness.
To participate in training new staff as appropriate.
Assist with marketing the company if and when appropriate.
QUALIFICATIONS/EXPERIENCE REQUIRED:
Medical/science background and relevant experience.
Ability and willingness to travel at least 50% of the time.(lnternational and domestic: fly and drive).
Ability to review and evaluate clinical data.
Computer literacy desirable.
Foreign language skills desirable.
Current full driving licence essential.
Good oral and written communication skills.
|
|
|
|
|
| |
|
|
Process Engineering Associate on a Contract basis. |
|
|
|
Category: |
Biotechnology, Pharmaceiuticals
|
|
|
Education: |
|
Position type: |
Full Time Employee |
Experience: |
9 years |
|
|
Area(s) of expertise desired: |
Chemical Engineering
|
|
|
Description: |
|
The position requires representing clients in bio and pharmaceutical industry in their capital projects. This translates into preparation and review of typical project deliverables, coordination between major project disciplines, operations, process development, QA, EHS, vendors/suppliers. Firm knowledge of Pharmaceutical and Biotech processes from design and operability perspective is a must.
|
|
|
Requirements: |
|
Degreed Process Engineer with 8 to 10 years of experience in pharmaceutical, biotech process design. Established knowlegde of biopharm project execution. Proven ability to generate and review process, mechanical, instrument and control deliverables. Good technical writing capability.
|
|
|
|
|
| |
|
|
Work in Singapore |
|
|
|
|
|
Education: |
|
Position type: |
Full Time |
Experience: |
|
|
|
Area(s) of expertise desired: |
Cardiology, Career Planning/Placement, Genetics, Oncology, Pharmacology
|
|
|
Description: |
|
All the expertise areas listed below.
|
|
|
Requirements: |
|
Able to work in Singapore
|
|
|
|
|
| |
|
|
|
| |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
מטפלת מאגר מטפלות לילדים , אופרייות
לוח
דרושים הגדול בישראל כולל אלפי הצעות עבודה | |
|
|
|
|
|
 |
|
