Opportunity for M.Pharm, M.Sc as Clinical Research Associate: SCRI - freshers

The Sai cr institute is a unique year-long education and mentoring program for hematology fellows and junior faculty at academic medical centers and offers a broad education about clinical research methods, research collaborations, statistical analysis, and managing the demands of family and career.

The goal of Saicrinstitute is to produce a group of researchers armed with ideas for clinical hematology research and the tools and access to resources to make their ideas a reality.

Post: Clinical Research Associate

 

Job Description:- A clinical research associate (CRA) runs clinical trials to test drugs for their effectiveness, risks and benefits to ensure they are safe to allow on to the market. They may work on new as well as existing drugs and are usually employed by either a pharmaceutical company or a contract research organisation (CRO) which works on behalf of pharmaceutical companies.

 

Required Skills : Pharma, biotech,Microbiology

 

Candidate Profile:
M.Pharm, B.Pharm, B.Tech(biotech), M.Tech(biotech), M.Sc(biotech), BDS, MBBS, BNYS, BAMS, BPT
Exp: 0-2 years

 

Additional Information:
Exprience: 0-2 years
Qualification: M.Pharm, B.Pharm, B.Tech(biotech), M.Tech(biotech), M.Sc(biotech), BDS, MBBS, BNYS, BAMS, BPT
Location: Chennai/ Bangalore
Industry Type: Pharma, Biotech, Clinical Data analyst, CRA
Last Date: 15^th January, 2015

 

Contact:
HR-team
91-9003448315
044-43520633
Email: saiclinicalrnd@gmail.com 

By Axis Placement Consulting hiring for Pharmacovigilance Graduates in Delhi/NCR, Faridabad, Noida

Qualification: B. Pharma Graduates with excellent Communication skills & willing to work in 24x7 Environment apply. Candidates should be Registered pharmacist & have good communication skills.
NO Master Degree or Diploma
Experience: 0 to 5 yrs.
Salary: INR 1,50,000 - 3,00,000 P.A
Role: Clinical Research Associate/Scientist

Contact @

Aakanksha:-  9711706614

Vacancy for Clinical Research Associate in Lonza

Lonza is one of the world's leading suppliers to the pharmaceutical, healthcare and life science industries. Products and services span its customers’ needs from research to final product manufacture. It is the global leader in the production and support of chemical and biological active pharmaceutical ingredients. Lonza is also the world leader in microbial control providing innovative, chemistry-based and related solutions to destroy or to selectively inhibit the growth of harmful microorganisms. In addition, Lonza is a leader in cell-based research, endotoxin detection and cell therapy manufacturing. Furthermore, the company is a leading provider of value chemical and biotech ingredients to the nutrition and agro markets.

Post: Clinical Research Associate-000003HP

Primary Role Responsibilities
1.· The CRA is expected to follow the policies, procedures, guidelines, and standards for excellence and professionalism established by LONZA.
· Additionally, this position will assure that all clinical and laboratory research activity adheres to policies, procedures and requirements.
· Preparation of Informed Consent Form (ICF), Case Report Form (CRF)
· Maintain on going communications with sites to provide information, queries resolutions,
· Follow and track clinical research milestones for assigned projects.

2. Assist QA in preparation and review of the Clinical operation SOPs and their associated documents.
3. Performs other study related tasks as assigned by managers.
4. Training of the personal on site for tissue collection.
5. Maintain audit, SOP and training compliance.

Candidate Profile
Maintenance of quality systems and cGMP compliance for the business by ensuring that all team members comply with processes, procedures and instructions for all activities in which the team participates.

Safety Responsibility
· Is knowledgeable and complies with all pertinent safety policies, rules and regulations.
· Ensure that all team members comply with safety rules and regulations.

Skill Requirements
Biological background (Masters) or equivalent 2-3 years experience in clinical research. Demonstrates high level of Customer Relationship Management.

Additional Information:
Location: Hyderabad
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: R&D
End Date: 10^th May, 2014

 Apply Online

 

Urgently Requirement For Clinical Research Associate / Coordinator in Zenith Service Provider

Experience required for the Job: 0 - 3 years

Job Location: Delhi/NCR

KINDLY BRING THE HARD COPY OF THIS MAIL, WITH ONE PASSPORT SIZE PHOTOGRAPH , YOUR ACADEMIC , PROFESSIONAL DOCUMENTS WITH ID AND ADDRESS PROOF.
Industry type:- RPO
Salary:- Best in Industry
Qualification:- B.Pharma, B.Sc, M.Pharma, M.Sc, Biotechnology, M.B.B.S., B.P.T., B.D.S. 
Skills:
* To plan, undertake and document study audits of the clinical studies to assess the integrity of the data and to determine whether the studies are planned, conducted and reported in compliance to GCP, SOPs and regulatory requirements
* To undertake systems audits and document specific audits to determine whether procedures and systems within the Clinical Research Department are adequate, relevant to current operational practices and compliant to GCP, SOPs and regulatory requirements.
* To undertake vendor audits.
* Prepare audit report and forward the audit observation to respective divisions.
* To prepare and reviews of SOPs.
* Responsible for induction and training of new employees and on going training of SOPs and GCP/GLP for the existing staff.
* To implement change control and document control procedures.
Interested candidates can directly walk in to change their carrier profile on mentioned address.
ADDRESS: ZENITH SERVICE PROVIDER, PLOT. NO. 2 N - 67 Bungalow Plot Near 2-3 Chowk Near to Apoorva Nursing Home N.I.T. FARIDABAD 
LAND MARK: - Near Vidya Niketan School 
WEBSITE: - www.zenithserviceprovider.com
ROUTE: By Metro approx 30 min. From Badarpur Metro Station 
By Train approx 2 Kms From Old Faridabad Railway Station 
By Bus Approx 2 Kms From Dusshera Ground Bus Station / Metro Chowk N.I.T. Faridabad. 
By Air Approx 40 Kms From Indira Gandhi International Airport

Come Down and attend face to face Interviews other details HRs will give you during Interview.
Please do not come without scheduling the Interview. 
Kindly Schedule your Interview with Jyoti and Amit @ 0129-6410393 / 09560448676

NOTE: WALK-IN with updated resume .Only the mail recipients are allowed to attend the walk in. Do not send your resume; we would like to meet each one of candidate personally. If you have already attended for the personal interview with us then please ignore this mail. Kindly carry all your Xerox copy of Marks Cards. We outsource the opening services to candidates as per their profile. Conditions apply as per performing in the interview and Openings will be provided as available in Delhi/NCR and All Over India Basis, with reg. and need to carry all your documents for interview Candidates are advised to read the note completely and walk in if they are fine.

Walk In for the post of Clinical Research Associate at RMRIMS, Patna, India

Company Profile: The mission of RMRIMS, Patna is to provide technical support to the policy makers and implementers to combat the kala-azar disease at the ground level through conducting high quality research on diagnosis, treatment and control as well as capacity building to the different stakeholders. Besides Kala-azar, the Institute is rolling forward to broaden its research focus on HIV/AIDS, tuberculosis and other tropical diseases and come forward as a centre of excellence on the land of Bihar.   
 
Eligibility: M. Pharma (Clinical Research)

Last Date: 29/10/12

For more detail: http://www.icmr.nic.in/icmrnews/rmrims_posts.pdf

Walk In for the post of Research Associate at IICB, Kolkata, India

Eligibility: PhD in Life Sciences
Date: 23/2/12
For more detail: http://www.career.iicb.res.in/

Opening for the post of Clinical Research Associate at SIRO Clinpharm, India

Company Name: SIRO Clinpharm

Company Website: http://www.siroclinpharm.com

Qualification: The incumbent should be Doctorate/Master's/Bachelors Degree in Science with minimum two years of experience on Phase I/II/III trials is must in the capacity of CRA either in CRO or a bio-pharmaceutical company. Basic understanding of the drug development process and understanding of clinical research process and ICH GCP is must.

The core responsibilities for the position would be Site Monitoring:

• Perform study site qualification visits, participate/conduct investigator's meeting and site initiation visits in coordination with the project manager and/or medical monitor
• To ensure all assigned studies follow SIRO/applicable SOPs, GCP and local regulations. Ensure regulatory documents are available, complete and current and submitted as per timelines.
• To identify, define, coordinate and conduct site study training. Perform regular monitoring visits to site, prepare monitoring reports and maintain audit readiness at the site level.
• Responsible for recruitment and propose alternative solutions if the predefined objectives are not met, either in the terms of patient number or timelines.
• To resolve all data queries or other study related queries from the site within timeframe.
• Conduct site close out and assure appropriate archival of controlled documents.

For more details: Click here

Opening for post of Clinical Research Associate, Clinical Research Manager, Clinical Data Management Lead, Support Specialist, Clinical Quality Specialist at Progressive Life Sciences, New Delhi, India

Company Name: Progressive Life Sciences

Qualifications: MBBS/M.Pharmin/MD health related field

Location: New Delhi, India

For More Details click here: Click here