www.careworldservices.com Care Worldwide Site Management : CRA, CRC, SAS, NURSE, INVESTIGATOR

[Care Worldwide]

Company Name : Care Worldwide Site Management Organization
Email ID : sven@careworldservices.com
Job Country : India
Job Position : Clinical Research Associate, Sub-Investigator, Princiipal Investigator, Clinical Research Coordinato
Job Location : Hyderabad, Ahmedabad, Cochin, Chennai, New Delhi, Bangalore, Mumbai, Pune, Kerala, Hyderabad, Chennai
Vacancy Type : Full Time and Part Time
Gender Preference : Any [ Male / Female ]
Number Of Vacancy : 0-50
Industry Area : BioTech/R&D/Scientist

Job Requirement:
We are looking for a team play, with good problem solving skills, excellent written and communication skills, and excellent organization and time management skills. Job Vacancy open in Chennai, Kerala, Hyderabad, Bangalore, Mumbai, New Delhi, Gujarat, Punjab

Key Skills : CRA,DATA MANAGEMENT,CRC,QA,NURSE,MD,MBBS,MS
Salary (Per Month) : Negotiable
Work Experience : 0 - 0 Years
Qualification : Bachelor Degree, B.Pharma, B.Tech/B.E, MBBS, Master Degree, Post Graduate Diploma, MS, M.Pharma


Company Profile
We are a Site Management Organization with our headquarter in New York, USA and we have sites in various countries around the world. Our Purpose: To support the innovation & development of new drugs & devices through clinical trials in partnership with pioneering pharmaceutical, biotechnology, and medical device industries. Our Goal: To provide quality service, responsiveness, and results to our customers striving to be the finest resource & meeting their specific and unique needs.

PLEASE SEND YOUR CV/RESUME THROUGH EMAIL: sven@careworldservices.com
WRITE SUBJECT: RESUME FOR CARE SMO
WEBSITE: www.careworldservices.com


NOTE: DON'T REPLY ON THIS THREAD

HR - CARE SMO

[mskavi]

Company Name: Care Worldwide Inc. Site Management Organization
Website: www.careworldservices.com
Location: Headquarters - New York, Local Job: INDIA

Designation: CRA, CRC, SAS, NURSE, PRINICIPAL INVESTIGATOR, SUB INVESTIGATOR

Clinical Research Associate

MBBS, PhD, Pharmacist, Biotechnology
Experience 2 yrs or more as Clinical Research Monitor

Clinical Data Manager clinical
Computer Programming experience 2yrs or more

Quality Assurance:
Bachelors, Masters in Science


Job Details:
We are a Site Management Organization with our headquarter in New York, USA and we have sites in various countries around the world. Our Purpose: To support the innovation & development of new drugs & devices through clinical trials in partnership with pioneering pharmaceutical, biotechnology, and medical device industries. Our Goal: To provide quality service, responsiveness, and results to our customers striving to be the finest resource & meeting their specific and unique needs.

Job Requirement:
We are looking for a team play, with good problem solving skills, excellent written and communication skills, and excellent organization and time management skills. Job Vacancy open in Chennai, Kerala, Hyderabad, Bangalore, Mumbai, New Delhi, Gujarat, Punjab

Principal Investigator:

MD/MS Licensed in its country of origin with 3-4yrs experience in the postgraduate therapeutic area with or without experience in clinical trials

Sub-Investigator:

Fresh MD/MS/MBBS graduates with no experience

Project Manager:

Phd/ MBBS / Nurse Practioner with 5 yrs experience in clinical trials

Clinical Coordinator:

Nurses BSN/Gen Nursing with 2yrs experience in nursing field

Lab Technician:

Lab Tech with Phlebotomy and Lab procedures experience to handle testing independently for 10 clinical sites at one time

Key Skills : CRA,DATA MANAGEMENT,CRC,QA,NURSE,MD,MBBS,MS
Salary (Per Month) : Negotiable
Work Experience : 0 - 0 Years
Qualification : Bachelor Degree, B.Pharma, B.Tech/B.E, MBBS, Master Degree, Post Graduate Diploma, MS, M.Pharma

SEND CV THROUGH EMAIL: sven@careworldservices.com

http://careworldservices.com/

India
4th Floor Rectangle No.1,
Behind Marriot Hotel Saket
Commercial Complex D4, Saket
New Delhi 110017 India

Branch Office:
15th Floor, Eros Corporate Tower Nehru Place New Delhi 110 019 India

Bombay Maharashtra
India: Nandkumar Ghadge:Clinical Research Associate
Metropolitan Business Center
Ground & First level Trade Center
Opposite MTNL Building
Bandra Kurla Complex Bandra Mumbai 400051

Bangalore
India:Chinmaya Mahapatra: Clinical Research Associate
Level 14 & 15,Concorde Towers,UB City, Vittal Mallya Road, Bangalore 560001

[Opera Srl]

Clinical Research Area Coordinator Profile
A Clinical Trial is a scientific study on the effects, risks, efficacy and benefits of a medicinal product (as drug, biotech or medical device). Trials need to be carried out before a product is registered by Local Regulatory Authority and arrive on the market. They are performed at various phases, and include: trials on healthy humans; trials on patients with a disease; and studies conducted after the launch of a new product with the aim of monitoring safety and side effects during large-scale use.
Usually clinical trials are conducted by pharmaceutical companies, Scientific Institutions or Contract Research Organizations (CROs) which act on behalf of them.
Opera Srl, a CRO located in Genoa, Rome and Bucharest, is currently recruiting for a Clinical Research Area Coordinator reporting to the Head of Clinical Operations for our team located in Genoa, 5 days work week.
Clinical Trial Manager, Clinical Research Associates, Data Managers will report to this position.
Opera Srl is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace.

Job Scope:
- Partner with the Sponsor Project Manager, the Head of Clinical Operation and the Statistician to elucidate study design and protocol development.
- Collaborate with Opera team members (Clinical Research Associates (CRAs), Clinical Trial Manager and Data Managers) for monitoring the trial throughout its duration, which involves visiting the study Centers on a regular basis.
- Maintain timely and effective communication among Opera team members and Site staff.
- Liaising with the Investigators and with the Sponsor Project Manager on conducting the trial.
- Assure the Investigator integrity and safeguard the rights, safety and wellbeing of all trial subjects.
- Assist in the preparation of study documents (i.e. Investigator Brochure, Investigational Medicinal Product Dossier) and tools (Case Report Forms) as requested.
- Manage Regulatory Authority and Ethics Committee applications and approvals that oversee the research. In addition liaise with the Authorities as appropriate on amendments and questions relating study activities.
- Interact closely with the Investigator Site to manage the trial level logistics ensuring compliance with protocol, Sponsor SOPs and completion according to study timelines.
- Coach the Investigator Site in GCP compliance/process improvement as necessary.
- Assure recruitment plan is in place.
- Assure and verify timely reporting of AEs/ SAEs and Protocol Violations.
- Assure and verify accurate completion of Data Clarification Forms.
- Document and tracks the resolution of all outstanding site-specific protocol-related issues from visit to visit.
- Attend Clinical Meetings according to the Project Monitoring and / or Training Plans.
- Provide Project Management of Final Report writing, including personal contributions to appropriate sections and management of scientific peer and administrative review / approval process.
- Take ownership or contribute to manuscripts.

Required Qualifications and Experience:
- Life Science degree with postgraduate training (PhD preferred), with interest in Clinical Research.
- Master in Clinical Research is appreciate.

Core Skills:
- Minimum of 3 years of related clinical research experience including 2 years of clinical trials monitoring and 1 year minimum of supervisory experience.
- Competent use of English.
- Well versed in biological sciences and clinical research methods.
- Demonstrated record of scientific writing and expertise to review and evaluate medical data.
- Knowledge of regulatory requirements ( GCP guidelines, ICH) and ethical issues (Helsinki Declaration).
- Previously worked within a team with project management skills: ability to prioritize work and to multi-task, excellent attention to detail, demonstrate a pro-active attitude, work under pressure.
- Excellent interpersonal and presentation skills and ability to interact at all levels in this facing role.
- Proficiency in Microsoft applications (MS Excel, Word, Power Point) and Internet.
- Applicants should be residing in Genoa.
- Any gender and nationality.


What is offered:
- Competitive salary.
- Substantial further performance related bonuses.
- Career prospects.
- Ongoing learning and training.
- Working in a team dedicated to one of the most exciting clinical development in EU.
- Long term job.

[skishore]

Dr. SAUMYA KISHORE

1.CAREER OBJECTIVE:-
My objective in life is to work diligently and honestly to achieve the desired targets.Looking forward to work in drugs R&D or production environment where I can prove myself with best of my knowledge and experience in the field of medicine.


2.EDUCATIONAL QUALIFICATIONS:-
Qualifications Institute/Board/University Year of Passing Percentage
High School K.V.Air Force,Bareilly, 2001 69 %
C.B.S.E
Intermediate K.V.Hebbal,Bangalore 2003 74.2%
C.B.S.E
B.D.S K.C.D.S,Bangalore 2008 61 %
(Bachelor of (Rajiv Gandhi University
Dental Surgery) of Health Sciences)


3.PROJECT UNDERTAKEN (s):-
- Working experience in K.C.D.S, Bangalore for 1 year
- Have worked in a clinic for 6 months .


4. KEY SKILLS :-
- Good working and communication skills.
- Inquisitive,and quick learner.
- Problem solving and Decision making.
- Key Assets - Honesty, Sincerity , Diligency.


5.PERSONAL DETAILS :-
Date of Birth :- 19/09/1985
Interests :- R&D, Reading, Sports.
Languages :- Hindi, English


Dr. Saumya Kishore

[raut1982navneet]

Dear Hiring Manager,

I'm writing in response to the position of Clinical Research Co-ordinator ,advertised as being open with your organisation at this time. I'm highly capable for CRC.
I'm able to manage multiple trials simultaneously,from inception to completion, as well as continue to follow up with patients regarding on going & post trial examinations. My documents skills are well developed & I'm able to prepare informed patient consent forms, IRB submissions, Correspondence, Public relations relcases,& Patient medical records
So,kindly let me know if any vacancy in your Organisation as CRC.

Thanku & Regards,

Mr.Navneet Raut
Cancer Clinic
Nagpur.

[Guest]

ASWATHY. P.A, M.Sc, CPCR (Pursuing)

Email : aswathy.ashok134 AT gmail.com


CAREER OBJECTIVE :

Seeking a position as Clinical Research Coordinator/ Trainee in the clinical operations. I believe I can bring the broad "soft" skills you need in a candidate that would represent the values of the organization.
MY MOTTO : To Excel, Compete and Win, wherever I am.

EDUCATION :

Certificate Program in Clinical Research and Regulatory Affairs(CPCR), Mir- IFCR, Kochi.
M.Sc Industrial Biotechnology, Karpagam Arts and Science College Coimbatore (81%).
B.Sc Biotechnology, G.R.D College of science, Coimbatore (73%).
Higher Secondary, R.V.H.S.S, Thalassery (76%).

Completed Three months Internship in Phase 3 study at Regional Cancer Centre (Head & Neck Department), Trivandrum.


SUBJECTS EXPOSED

1) Regulatory Affairs – ICH-GCP, FDA, Schedule Y.
2) Research Methodology
3) Biostatistics and Computer Applications
4) Clinical Trial Management
5) Pharmacovigilance
6) Familiar with e- CRF entering (Oracle version), Paper CRF, Taking Informed Consent with subjects and other documentation works.




SKILLS AND ABILITIES :

- Ability to make presentations.
- Ability to understand problems and solve them.
- Leadership Skills
- Team Player


ABOUT MYSELF :

My pursuit of Biotechnology has ended up in Clinical Research Management, where I feel very proud to be part of. I believe, I have the skills and the personal qualities required to successfully carry out the duties and responsibilities of a Clinical Research Professional.


TRAINING AND SEMINARS :

- Conducted a presentation on History of Clinical Research at Mir- IFCR Cochin.
- Organized a National Conference on “Challenges in Clinical Research” with Mir-IFCR India.
- Conducted a Presentation on Biosimilars at Mir- IFCR Cochin.
- Attended Seminar on “Regulations Meet Practice & Advanced GCP” conducted by Amrita Institute of Medical Science in collaboration with Pfizer.
- Special Training on “Research Methodology” by Dr. Hari Dayal, Adjunct Professor, University of North Texas.
- Training on Biostatistics by Prof. Dr Anil. C. Mathew, PSG College Coimbatore.
- Specialized training on Pharmacovigilance by Dr. Santhosh Joseph, MD (Pharmacology) MIMS, Tamil Nadu.
- Undertaken Training at Karpagam College of pharmacy, CBE in Tablet preparation and analyzing the dissolution and HPLC.

EXTRA CURRICULAR ACTIVITIES :

- Singing and listening to music (Carnatic music).
- Playing Badminton.
- Gardening.

[Guest]

I am working as CRC in a Famous hospital and managing 8 ongoing trials. I want to relocate some where. please Send details if any vacancy for these post.