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Health And Life Sciences ( H&LS ) - Study programmers required for Bangalore

Job Description
Graduates/ Postgraduates in with 1 to 3 years of working experience in building and reviewing study based on specifications may apply. Experience in creating paper or eCRF using Framework, Adobe Acrobat or Microsoft Word or EDC/RDC tools (OC, RAVE) and working knowledge in study database building and validations in EDC/ RDC/ CDM tools is mandatory.

Required Qualifications:
Graduates/ Postgraduates in Life Sciences/ engineering/ computer applications

Required Experience:
1+ YEARS
experience in Clinical SAS
candidates from Clinical data management who are Oracle programmers and PLSQL.

Our client, a global clinical research organization offering cost-effective and time-sensitive solutions for conducting clinical studies have the following requirements

Our clients are a leading independent provider of Continuing Medical Education (CME), Medical Information and
Pharma Marketing Strategy services. They serve Medical institutions, Pharmaceutical companies and CME /
Pharma Marketing Services providers in India and USA. They have immediate openings for the following skills :

The project manager will head a team of medical content researchers and medical writers. The team will be assigned
CME and Content projects that have been entrusted to the company. He/ She will co ordinate and contribute to the team
activities in maintaining quality of project and adhering to time lines. He/ She will also be co ordinating with senior specialist
in all specialties, Medical associations and pharmaceutical companies on various CME and Content projects.

The prospective candidate will be below 30 years and will be a MD Pharmacology preferably or a MD in any other discipline.
The candidate should be academically inclined. He/ She will be reporting to content head.

The prospective candidate will be currently General Manager and above in a pharmaceutical company. He would have had good exposure to Marketing and Sales.

He should demonstrate innovative thinking in using science as a cutting edge tool to promote ethical brands in the marketplace. He should have a track record of having successfully done things differently.

He should be a self-motivated individual with energy and drive to provide the inspiration to a young team to spur them to success.

The position calls for a very dynamic candidate below 45 years, with post graduate qualifications in Medical Sciences and Business management,. Who is currently heading medical services functions of a leading pharmaceutical company as GM/VP.Exposure to Cme products and pharma marketing services will be an advantage.

Our Clients are a reputed full service Clinical Research Organization and Reputed companies in Pharmaceutical Industry. They are providing a comprehensive range of clinical services, clinical trials and clinical research services to healthcare and pharma companies and inhouse Reserch and development. They require the following personnel to meet their ambitious growth plans.Click the Links below to View Job requirement, qualifications and Job descriptions:

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J2EE - Developers / Senior Developers with HL 7 Experience

3-4 years of experience in J2EE, Websphere with minimum 1 year in Health Care domain.
1 Year experience in HL 7 Health Level 7 (HL 7) standards and Knowledge in XML is essential. Email Resume: kbschennai@kbsconsultants.com

Clinical Trials Project Manager

Responsible for management of clinical trials / programmes throughout Asia. The candidate should possess the following:

· A Master Degree in Medical, Scientific or Nursing discipline
· With 6 years and above experience in managing clinical projects across Asia would be required
· A thorough knowledge of GCP and the relevant Asian Regulations
· Availability to travel frequently throughout Asia
· Ability to successfully manage projects teams
· Possess excellent organizational and communication skills with a strong customer focus

Email Resume: kbschennai@kbsconsultants.com

Senior Clinical Research Associate

Responsible for planning, initiation and monitoring of clinical trials to international GCP standards throughout Asia. The successful candidate must have the following:

· A Master Degree or equivalent in Medical, Scientific or Nursing discipline
· 4 to 6 years of clinical trial experience is required
· Availability to travel frequently throughout Asia
· Excellent attention to detail
· Strong communication skills and computer literacy

Email Resume: kbschennai@kbsconsultants.com

Biotech and Pharmaceutical News & Jobs
Pre Clinical Research Activities
Description
The incumbent candidate plans, Oversees, designs, develops, and monitors clinical research and evaluation projects.
Will be responsible to Monitor and/or supervise the monitoring activities of clinical trials for new products, product enhancements, and product process changes to ensure adherence to any and all applicable regulations, policies, and any other applicable procedures.
He will be responsible for maintaining the integrity of clinical data, and for ensuring that project timelines are met.

JOB RESPONSIBILITIES:

Responsible for compliance with all applicable regulations, policies, and any other applicable procedures.
1. Will Recruit, mentor, coach and develop a team with required talent.
2. Provide general guidelines and direction to managers.
3. Build strategic partnerships to further the business interests of the organisation.
4. Make informed operational decisions and execute them with a strategic perspective.
Requirements
POSITION ACCOUNTABILITY/SCOPE:
This is a senior position which requires out of box thinking and analytical abilities.
Leadership skills and man management
Fully conversant with Clinical research and Clinical Trial activities

Clinical Research Associate

Responsible for planning, initiation and monitoring of clinical trials to international GCP standards throughout Asia. The successful candidate must have the following:

· A Master Degree or equivalent in Medical, Scientific or Nursing discipline
· 2 to 4 years of clinical trial experience is required
· Availability to travel frequently throughout Asia
· Excellent attention to detail
· Strong communication skills and computer literacy

Email Resume: kbschennai@kbsconsultants.com

Clinical Trial Assistant

Responsible for assisting Senior Clinical Research Associate/Clinical Research Associate for planning, initiation and monitoring of clinical trials to international GCP standards throughout Asia. The successful candidate must have the following:
· A Master Degree or equivalent in Medical, Scientific or Nursing discipline
· 1 to 2 years of clinical trial experience is required
· Excellent attention to detail
· Strong communication skills and computer literacy

Email Resume: kbschennai@kbsconsultants.com

Our clients based in Australia require Seebeyond Consultants with experience in HL7
Seebeyond Experience in ICAN 5.0
Experience of working in healthcare Sector with HL 7 Standard
Apart from that good J2EE experience and background, atleast 4-5 years experience.
Good communication Skills Email Resume: kbschennai@kbsconsultants.com

Project Manager Clinical Research
Qualifications & Experience
Phd/MSc in Life sciences or pharmacy with 5-7 years of clinical researchexperience

Job Description and Responsiblities
Handling complete Project Management for assigned projects, tracking project budget, Ensuring compliance to SOPs/Protocols/ICH GCP/local and International Regulations, Training of CRAs and Investigators, ensuring quality and speed for assigned projects, preparing for inspections and audits. Any other duties assigned from time to time Email Resume: kbschennai@kbsconsultants.com

CRA - Clinical research Associate (Experienced)

Qualifications & Experience
Msc/BSc in Life science or pharmacy with 1-3 years of clinical research experience

Job Description and Responsiblities
Handling all clinical trial related acctivities, right from Identification of sites, organising Investigators' Meetings to study start,monitoring and study close-out activities. Ensuring appropriate storage and Inventory Management of trial supplies. Comply with SOPs/Protocols/ICH GCP/local and International Regulations, Training of Investigators and Team, ensuring quality and speed for assigned projects, preparing for inspections and audits. Any other duties assigned from time to time. Email Resume: kbschennai@kbsconsultants.com

Medical Writer
Qualifications & Experience
Msc in Life Sciences/MBBS 1-3 years of clinical research experience and exposure too Medical Writing.

Job Description and Responsiblities
It is important for the medical writer to have a broad understanding of the statistical theory in evidence-based medicine, without necessarily following all the mathematical calculations. Preparation of clinical protocols, investigator brochures, monitoring plans, patient and study site education materials, clinical program newsletters and clinical study reports. Preparation of annotated bibliographies and literature reviews, manuscript preparation from source data; editing and review of physician-prepared manuscripts; editing and quality-assurance of manuscripts, format posters, meeting handouts, presentation compendia. Development of in-house clinical monitor training programs and curricula; therapeutic area monitor training materials, CME educational brochures, slide kits, and training materials with the help of Project Managers Email Resume: kbschennai@kbsconsultants.com

Quality Analyst - Clinical Trial Quality

Qualifications & Experience
Phd/MSc in Life sciences or pharmacy with 5-7 years of experience in Clinical Trial Quality Department Email Resume: kbschennai@kbsconsultants.com

Clinical Pharmacologist
Qualifications & Experience
MD Pharmacology Email Resume: kbschennai@kbsconsultants.com

Analyst Bioanalytical Lab
Qualifications & Experience
M Pharm/MSc in Analytical Chemistry with 0-1 years in Bioanalytical Lab

Job Description and Responsiblities
Performing bioanalytical work including method development, validation and sample analysis as per the protocol in compliance with GLP. Maintaining instrument logbooks. Performing equipment troubleshooting (in case of malfunctions), periodic calibration and maintaining relevant records in coordination with maintenance department. Sample tracking (receipt, check, storage, shipment, disposal) and maintaining records theirof. Daily monitoring and recording of temperature, humidity and pressure in laboratory. To ensure cleanliness and neatness in the laboratory with the help of laboratory assistance. Maintenance of records/logbooks for water analysis, periodic checks of safety related aspects like fire extinguisher, first-aid box, eyewash etc. Email Resume: kbschennai@kbsconsultants.com

Bioanalytical Executive

Qualifications & Experience
M Pharm/MSc in Analytical Chemistry with 1-3 years Experience in Bioanalytical Lab

Job Description and Responsiblities
Responsible for all matters related to Bioanalysis in-line with GLP requirements and periodic review of SOPs. Development of protocols, co-ordination with the Scientific Manager/Head-BR for protocol approval. Conducting bioanalytical activities (development, validation and sample analysis) as per approved protocol. Maintenance of bioanalytical records and relevant logbooks. Planning and supervision of study requirements. Supervising day-to-day activities conducted by analyst in the laboratory and guiding/training the analysts. Procurement and maintenance of reference standards, reagents, analytical columns etc. Ensuring calibration and maintenance of equipments (HPLC, LC-MS/ MS etc). Email Resume: kbschennai@kbsconsultants.com

Scientific Manager
Qualifications & Experience
Ph.D./M.Sc. in Analytical Chemistry /M. Pharm. with 3-5 years experience

Job Description and Responsiblities
To supervise day-to-day operation and personnel performing different functions in the laboratory with respect to Bioanalytical projects. Training the personnel in Laboratory. Review of data and reports. Co-ordination with Clinical, Regulatory and Data Management and Administration departments for execution of projects. Liaison with clients whenever necessary. Implementation of systems adhering to GLP requirements in coordination with QA. Review of method development and validation protocols, method validation reports and Bioanalytical reports. To prepare for internal and/or external audits. To review and approve of Standard Testing procedures (STP). Email Resume: kbschennai@kbsconsultants.com

Phlebotomists

Qualifications & Experience
DMLT
Job Description and Responsiblities
Canula insertion & removal, blood collection, monitoring of subjects for AE, dosing, CRF completion, maintining of ICU equipments, Email Resume: kbschennai@kbsconsultants.com

Custodian Pharmacology

Job Description and Responsiblities
Graduate with 1-2 Years of experience in a Human Pharmacology Unit volunteer coordination, physical check, monitoring of volunteers during study, check in process, check out process Email Resume: kbschennai@kbsconsultants.com

Medical Officer & Duty doctor

Qualifications & Experience
MD/MBBS in general medicine

Job Description and Responsiblities
perform physical check, ECG, X-ray, coordinate with central lab for results, dosing of medication, safety analysis and AE monitoring Email Resume: kbschennai@kbsconsultants.com

DMLT Technicians
Qualified DMLT Technicians with relevant skills and experience Email Resume: kbschennai@kbsconsultants.com

Clinical Data entry operators

Job Description and Responsiblities
Data entry operators with Life sciences(Bsc, Msc, B.Pharm etc) back ground and clinical data entry experience
Clinical / medical data entry, query initiation Email Resume: kbschennai@kbsconsultants.com

Quality - Data capture
Qualifications & Experience
Experienced CDM quality supervisors with life sciences background

Job Description and Responsiblities
Assuring 100% quality of captured data, query resolution, initiating and managing the quality system for a CDM unit Email Resume: kbschennai@kbsconsultants.com

Report Executives Reporting clinical statistical
Qualifications & Experience
People with Life sciences(Bsc, Msc, B.Pharm, Medical etc) back ground and clinical report writing experience

Job Description and Responsiblities
Writing reports statistical, medical, proposals, regulatory etc., Email Resume: kbschennai@kbsconsultants.com

Documentation Librarian

Job Description and Responsiblities
Preparing, reviewing, all quality, process, systems related documents. Initiating, maintaining, updating etc of the complete CDM documentation including SOP's and managing related library function (10%) Email Resume: kbschennai@kbsconsultants.com

Clinical Data Manager

Qualifications & Experience
M Pharm/BPharm/Life sciences Graduates with Experience in Clinical Data management

Job Description and Responsiblities
Manage, Co-ordinate, motivate and deliver the CDM objectives of clean data on time including project management Email Resume: kbschennai@kbsconsultants.com

Biostatistician
Qualifications & Experience
PhD/ MSc in Statistics with specialisation in Biostastics with experience in working with drug discovery and development teams

Job Description and Responsiblities
Statistical planning, analysing, review, reporting, quality checking of data received etc., Email Resume: kbschennai@kbsconsultants.com

Biostatistics Manager

Qualifications & Experience
PhD/ MSc in Statistics with specialisation in Biostastics with experience(5-8 yrs) in working with drug discovery and development teams

Job Description and Responsiblities
Manage, Co-ordinate, motivate and deliver the Biostatistics team's objectives of statistical reports on time including project management Email Resume: kbschennai@kbsconsultants.com

Support staff Clinical research data management
Job Description and Responsiblities
Assist in various documentation activities (preparation of report/records, coordination with printer procurement of stationary and office requirements). To call for quotations, compare the quotation for the best available prices and release the purchase order for the items required. Tracking of inventory (logistics). Email Resume: kbschennai@kbsconsultants.com

JOB DESCRIPTION

Position Title: Business Development MANAGER
Department: Business Development – Clinical Research
Reports To: COO - Clinigene

Primary Position Purpose Summary
Oversees the contract development and approval, proposal development, change order management and clinical project feasibility processes within Business Development. Provides sales training to BD staff and provides strategic BD support to sales team as it relates to eServices initiatives. Serves as point person for strategic alliances with technology partners. Supports BD staff with creative solutions, coordination, input and dispute resolution.

Primary Job Responsibilities
1. Manages and trains members of the BD staff
2. Provides oversight for development and quality of all proposals
3. Provides oversight for contract and change order development, negotiation and approval
4. Provides oversight for patient recruiting (e.g., MMG) and technology (e.g., PHT) alliances
5. Facilitates development of clinical feasibility process and associated incorporation into proposals
6. Tracks all proposals, contracts, change orders and other BD documentation
7. Participates in the planning and execution of company sales activities
8. All other projects as assigned

Key Skills (list 3-5 skills required to perform job successfully):
1. Excellent communication skills (interpersonal, written, verbal, formal presentation)
2. Experienced negotiation skills
3. The ability to work with and manage people
4. Ability to perform overnight business travel, up to 50%
5. Excellent persuasive/selling skills

Experience:

1. Minimum of seven years sales experience, at least three of which are in the CRO industry
2. Minimum of three years management experience and at least one year of P/L responsibility
3. Demonstrated understanding of Phase I through Phase IV drug development

Education (degree) or Certifications:

1. Advanced degree in an appropriate scientific or business discipline (doctoral degree or MBA degree preferred)
Email Resume: kbschennai@kbsconsultants.com

KBS consultants
Flat H,Kulothungan Apts,No, 5 Natesan Road
Ashoknagar, Chennai 600 083 India
Phone: +91-44 2489 5341 / 2371 9622
email:kbschennai@kbsconsultants.com

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