Careers in Clinical Research

July 7, 2008

Job : Clinical Research Co-ordinatoor CRC ,Excel Life Sciences Pvt. Ltd.

Filed under: Jobs — clinnovo @ 12:12 pm

Job Description
PI/site identificationAssess manpower need & infrastructure capabilitiesTimely enrollmentInteract with Sites : Interact with PIs and other study members on a regular basisDiscuss potential issues and suggest corrective action.

Desired Candidate Profile
Experience:0 – 2 Years
self starter Excellent communication Able to mannage & interact with Investigator Some medical knowledge.

Contact Details
Company Name:Excel Life Sciences Pvt. Ltd.
Website:http://www.excellifesciences.com
Executive Name:Prachi
Email Address:prachi@excellifesciences.com

July 4, 2008

Job- SAS Administrators

Filed under: Jobs — clinnovo @ 10:51 am

Positions : SAS Administrators
Requirement:- Experience : 3 – 10 Yrs
Location : Pune
Contact
DEV 022-67135191
dev@ssn.co.in

Job-DOC-Medical Writer (0-3yrs)-Novartis,Hyderabad

Filed under: Jobs — clinnovo @ 10:47 am

Job Description
To support and/or lead activities related to reconciling, writing, editing and/or managing the production of high quality clinical documentation (e.g. Clinical Study Reports and Summary Documents) for submission to regulatory authorities in support of marketing applications.

Desired Profile
PhD in Life Sciences/Applied BiologyMD in Internal Medicine/ PharmacologyMBBS, MPharm, MSc by Research
Experience: 0 – 3 Years
Contact
Suresh Kolaham
Novartis Healthcare Pvt Ltd
Telephone 040-665676596

Job :Clinical Trial Analyst (0-3 yrs exp)Indegene LifeSystems Pvt Ltd

Filed under: Jobs — clinnovo @ 6:01 am

Job Description
1.Review of various clinical trial protocols and source documents.2.Clinical trial data analysis, tagging and updating the database.3.Advise data management staff on trial parameters, database designs, and validation of critical data.4.Reports progress and changes in clinical trials.5.Statistical analysis and competitive analysis of trial results.

Qualifications 1.Should have a qualified MBBS, BDS, M Pharm, B Pharm Degree. 2.A strong educational background in clinical research.3.Computer skills including use of Microsoft word, excel and power point.4.In depth therapeutic and clinical research expertise as well as knowledge of GCP/ICH and applicable regulatory guidelines.

Contact
Website:http://www.indegene.com
Executive Name:Srihari.S
Indegene LifeSystems Pvt Ltd
Email Address:careers@indegene.com
Telephone:91-080-40787557,40787556
Fax:41267704
Reference ID:CTIP

July 3, 2008

Job – Clinical Data Manager (CDM) II-Client of Kenexa

Filed under: Jobs — clinnovo @ 6:10 am

Experience – External:Minimum Relevant Work Experience – 2+ Years
Education‘Bachelor’s degree and / or other medical qualification or relevant DM experience

Key Accountabilities’Assume the ability to meet the requirements of a CDM I with a high degree of proficiency and autonomy’Maintain a positive, results orientated work environment, building partnerships and modeling teamwork, communicating to others in an open, balanced and objective manner’Take responsibility for specific tasks on projects, or acts as a Primary CDM on individual projects’Review key project documentation e.g. contract, protocol, project plan’Create, maintain and utilize study documentation including Annotated CRF, Data Validation Specifications, etc.’Perform clinical coding if appropriate to role within the project team’Develop project specific guidelines e.g. SAE handling, data validation’Perform QC of data processing activities’Facilitate and present topics at internal meetings’Train team members on select tasks’Obtain internal or external sign-offs when necessary’Utilize appropriate TIME codes as they relate to a particular task’Accurately estimate time needed to complete tasks within project timelines’Co-ordinate work among team members and liaise with internal and external contacts’Keep manager(s) informed about work progress and any issues to avoid surprises. Requires some interaction / supervision by Manager.

Company Name:Client of Kenexa

Website:
http://www.kenexa.com

Executive Name:nilamadhab.mahapatra@parexel.com

Email Address:Nilamadhab.Mahapatra@Kenexa.com

Telephone:99086 37066

July 2, 2008

Clinical Data Coordinator or Senior Clinical Data Coordinator-Bangalore

Filed under: Jobs — clinnovo @ 8:53 am

Job description : The Clinical Data Coordinator provides basic and some comprehensive data management expertise to data management team to provide efficient, quality data management products that meet customer needs. • The position is also expected to undertake team leadership activities under the supervision of the Data Operations Coordinator, Data Team Lead, or Functional Manager. • The person may serve as a Data Operations Coordinator (DOC) for one protocol with less then 5 operations staff (excludes DE) or a leadership role in a specific area or process on a large study with guidance. • The person may serve in the role of back-up to a Data Operations Coordinator or Data Team Lead. • The position calls for conduct of data review. • To write and resolve data clarifications. • To lead database audit team • To develop and test databases and edit specifications • To understand and comply with core operating procedures and working instructions. • To perform other duties and directed by the Data Operations Coordinator or Functional Manager. • To meet objectives as assigned. • To develop and maintain good communications and interpersonal relationships with the team.

Qualifications : A graduate degree or Post Graduate degree/diploma (preference in Health Science, Science, or Clinical) with 1 to 3 years of Clinical Data Management experience is preferred.

Contact :
Pallavi pharma@taskstaffing.com
Contact No- 079-40205060 Ext-251

July 1, 2008

Job -Clinical Research Physician @ Stempeutics Research Pvt Ltd

Filed under: Jobs — clinnovo @ 4:02 pm

Requirements :MD Pharmacology and MD Medicine from a reputed inst with 0 to 2 years of experience.
Job Profile:
1. Design and obtain approval of stem cell based treatment protocols from Inst Scientific Committee and implement through principal investigators
2. Devise pre and post therapy tests and manage patient record forms and patient follow ups for study data
3. Plan and Deliver Clinical Research studies in collaboration with medical inst or colleges and obtain funding
4. Identify gaps in current stem cell therapy and devise new treatment options in close association with the research groups.
5. Plan and Deliver pre clinical and phase I and II clinical trials as per ICH GCP norms with CRO as per business needs and budgeting
6. Make clinical presentations to customers/committees as a support to business development

Please apply directly atritu.arora@stempeutics.com subject line as CRP-Mnpl

June 30, 2008

Job: Clinical Operations Manager -PPD Pharmaceutical Development I Pvt. Ltd.

Filed under: Jobs — clinnovo @ 12:02 pm

Desired Profile :
5 years of Global trials monitoring experience. Candidate with line Management experience will be preferred.

Contact:Company Name:
PPD Pharmaceutical Development I Pvt. Ltd.

Website:
http://www.ppdi.com

Executive Name:Vikrant Dongre…
PPDI
801-804, Powai Plaza
Hiranandani Gardens, Powai
Mumbai – Maharashtra ,Singapore 400076

Email Address:hr.asia@europe.ppdi.com
Telephone:0091-022-25712963,25712900
Fax:25712999

June 29, 2008

Consultant – Oracle Clinical @ Oracle Corp,Bangalore

Filed under: Jobs — clinnovo @ 4:32 am

Requirements :IT undergraduate degree plus ideally post-graduate qualification in Life Science-related subject area 3+ years in IT or related discipline, ideally within the Life Science industry3+ years of one or many OLS applications experienceNot essential but an advantage to have experience in the following areasoOracle DatabaseoOracle DBA experience and/or OLS Applications Administration oProgramming background ideally in SQL, PL/SQLoDatabase structure of the OLS applicationsoEBS (eBusiness Suite) infrastructure and platform architecture

Contact
Pushpa Oracle India Pvt Ltd
Telephone 080 – 4029 8235
Email pushpalatha.sreenivasan@oracle.com
Website http://www.oracle.com

Job:Clinical Data Validator – MakroCare

Filed under: Jobs — clinnovo @ 4:15 am

Job Description : 3yrs of Phase I-IV pharmaceutical industry/CRO data management experience with Oracle Clinical & knowledge of GCP is required.Exp of electronic data capture & data validation programming is required.

Contact Details
Company Name:Makro Technologies (P) Ltd.
Website:http://www.makrotech.com
Executive Name:GN Rani/rani.galipall@makrotech.com
Email Address:careers@makrotech.com
Telephone:91-040-44335555

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