CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "SAE"

Sr. Clinical research Associate/ Director of clinical research

Can undertake most of the tasks and works independently. Very much focussed on the timelines and quite goal tending. Willing to help others in their prioritized tasks. Excellent planning, design and implementation. Highly experienced in writing reports and data analyses.

Ideal Companies: Pharmaceutical industries, Biotech companies, Research institutes, hospitals and for profit mid to large companies.

Tags for this Online Resume: Director of clinical research, Manager of drug safety, Senior clinical research associate, Regional clinical research associate

CTA

Seeking for a challenging career in a progressive organization offering the opportunity for contributing my skills services to the organization and personal growth and to work sincerely with maximum effort using best talents and with a challenge to achieve required goals and targets, abiding to the decisions of seniors and to earn a good reputation what ever required.

Tags for this Online Resume:  Develop, maintain and manage appropriate study documentation,  Developing, writing and presenting the clinical trial protocols,  Initiate, maintain and reconcile Trial Master File.,  Monitoring the trial throughout its duration which will involve visiting the Study centers on a regular basis to check the patient data in the case report forms (CRFs) and to sort out any problems which may arise.,  Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other Data collection tools by careful source document review Monitor data for missing of implausible data.,  Complete Serious Adverse Event (SAE) reporting, process production of Reports, narratives and follow up of SAEs and managing the clinical data intermilitently as per 21CFR USFDA guidelines,  Monitor study sites independently according to protocol monitoring guidelines, S.O.P.s, GCP and ICH Guidelines.,  Independently perform CRF review; query generation and resolution against established data review guidelines on client data management systems as assigned Perform other duties as assigned by management., , maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned

Drug Safety, Home based - 4 years exp - Argus - SAE processing - SUSAR reporrting - Narrative writing - coding using MedDRA & WHO Drug - Workflow management.

Looking for a full time permanent home based/regional position in Drug Safety.

Tags for this Online Resume: Drug Safety, Clinical Safety, Pharmacovigilance

Lead Project Manager- Clinical Trials

Proven expertise in managing teams, streamline project paths encompassing an understanding of scientific data, analysis and interpretation of results, clinical developability and commercial viability of projects.

Ideal Companies: Vertex Pharmaceuticals, Amgen Inc., Takeda Pharmaceuticals

Dynamic Department Manager

Organized,focused, and supportive departmental leader with excellent written and verbal commnuciation skills.

Ideal Companies: ALCOA, Honeywell, II-V, SAE, Berry Metal Products

Tags for this Online Resume: Engineering Quality Manager

Developer

I want to be the best in my field. My aim is to reach at the top of the ladder with my skills and expertise. Developing Web Based Software is my strength and wants to be known for my contribution to this industry. My ambition is sky high and every day it gets higher and higher.

Ideal Companies: gulfoilandgas.com

Tags for this Online Resume: C#

Senior/ Lead Clinical Reseach Associate - over 15 years experience monitoring, site management, medical record review, training/mentoring junior CRAs. database locks. regional clinical team leader

My goal is to secure a regional, home-based position in which I can use my knowledge of all phases of clinical research to develop tools to collect data (CRFs/edit checks; to verify the data (site management/monitoring), clean data (database locks)and to insure patient safety by assuring all AE/SAEs are reported, protcols and infomed consent are IRBs approved and adherence to all ICH guidelines and regulations.

Tags for this Online Resume: Lead CRA, Data Manager, Sr. CRA, Regional CRA

Project Engineer

I desire to utilize my skills and experience, which include but are not limited to organizing projects using a variety of software such as DCP for B.O.M. and Unigraphics for design concepts, as an asset to an expanding and upward mobile corporation. Having worked as a manufacturing engineer, I enjoy the challenge and responsibility of undertaking many projects. S.A.E. Member

Versatile Director Able to bridge the gap between operations and sales

Highly energetic director with exceptional leadership communication,sales,and problem solving skills.

Ideal Companies: I would be a great fit for privatley held corporations that wouldn't be afraid to utilize my diverse skills in a change management enviroment. A company not afraid to utilize both my saes and operations management skills.

Tags for this Online Resume: Director, Vice President, General Manager, Sales, Operations

Experienced Project / Safety Coordinator

To secure a challenging position in which my abilities and experience will be of value to an organization offering the opportunity for increased responsibility and knowledge.

Ideal Companies: Duke Univeristy, Merck & Co, Pfizer

Tags for this Online Resume: drug safety, clinical, research, coordinator

Sales Representative

any jobs related to sales and management.

Ideal Companies: Feed Company, San Miguel, Coke

Tags for this Online Resume: sales, sales rep

Post-sales Implementation

Tags for this Online Resume: Account Manager, Saes, Customer Service