Job as PRM Analyst at ICON

Post : PRM Analyst

Overview of the role    
* Recognize, exemplify and adhere to ICON's values which centers around our commitment to People, Clients and Performance.    
* As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.    
* Travel (approximately 10%) domestic and/or international.    
* The following responsibilities are expected to be competently and independently performed under the direction of the Manager of the Planning and Resource Management Department (PRM), applying theoretical knowledge and practical experience. The PRM Analyst I will directly contribute to the PRM department and share accountability for achieving department goals and objectives.

• Ensure requests requiring updates to the Resource Management database are actioned in a timely and accurate manner, according to established Service Level Agreement timelines.
• Support PRM Functional Leads according to established processes, including acting as backup during periods of absence and representing the PRM FL in resourcing discussions with operational leadership.
• Provide regular and ad hoc reports and information to operational leadership which is up to date, accurate and timely.
• Adhere to the existing process and develop competence by performing structured work assignments.
• Understand best practices and customer needs and apply this knowledge in the performance of the role.
• Work under supervision initially and become independent with experience.
• Work as backfill for colleagues in both functional lead and PRISM roles.
• Undertake other reasonably related duties as may be assigned from time to time

Role Requirements     

• To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.        
  - 6 months to 1 year experience in CRO will be an advantage.        
  - Knowledge in Clinical Research or Planning and Resource Management is desired.          
• Ability to liaise successfully with senior management, clinical project teams, other ICON departments (e.g. Finance, BD and HR) and clients if required.    
• Excellent communication and interpersonal skills.    
• Competent computer skills including knowledge of Excel and Database systems.    
• Due to the nature of this position it may be required for the employee to travel, therefore, dependent on the employee's location, the employee may be required to possess a valid Driver’s License 

Additional Information:
Location: Chennai
Reference: 042410
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CR
End Date: 5th September, 2016

Vacancy at Covance for post of Senior Associate, Drug Safety

Post: Senior Associate, Drug Safety

Job Description:
• Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or from a clinical trial. This includes, but is not limited to:

1. entry of safety data onto adverse event database(s) and tracking systems
2. review of adverse events for completeness, accuracy and appropriateness for expedited reporting
3. write patient narratives
4. code adverse events accurately using MedDRA
5. determine expectedness/listedness against appropriate label
6. identifies clinically significant information missing from initial reports and ensures its collection
7. ensure case receives appropriate medical review
8. prepare follow-up correspondence consulting the medical staff accordingly.
9. ensure all cases that require expediting reporting to worldwide regulatory agencies are processed swiftly and appropriately within required timelines
10. reporting of endpoints to clients, regulatory authorities, ethics committees, investigators and Covance project personnel, if required, within study specified timelines

Candidate Profile:
• Non-degree + 4-5 yrs relevant experience (or 2 yrs safety experience)*
• Associates Degree + 3-4 yrs relevant experience (or 1-2 yrs safety experience)*
• Associate degree RN + 2-3 yrs relevant experience (or 1-2 yrs safety experience)*
• BS/BA + 1-2 yrs relevant experience**
• MS/MA + 0 yr relevant experience**
• PharmD + 0 yrs relevant experience**

Degree preferred to be in one or more of the following disciplines: Biological Sciences, Pharmacy, Nursing, Life Sciences, and Chemistry.

Experience:
*Safety experience includes actual experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions.
*Relevant experience includes experience in the pharmaceutical, biotechnology, or CRO industry, partly in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Data Monitor, Regulatory Affairs, or Quality Assurance.

Additional Information: 
Requisition ID: 59013BR
Location: India
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Clinical Research

Invitation for the post of Product Manager - Upstream Technology in GE Healthcare

GE Healthcare, $17 billion unit of General Electric Company (NYSE: GE), employing more than 46,000 people worldwide and serving healthcare professionals in more than 100 countries. We believe in our strategy - and we'd like you to be a part of it. As a global leader, GE can bring together the best in science, technology, business and people to help solve one of the world's toughest challenges and shape a new age of healthcare.

Post: Product Manager - Upstream Technology

Purpose    
The primary responsibility of product manager role is to provide multifunctional support including to the sales team in promoting Upstream product portfolio to the biopharma industry. To provides application support in the form of technical product presentations, query resolution, coordinating with the global team and training to the industry and academia. The position is in a highly dynamic group and provides many opportunities for individual career development.

Job Description
1. The management of a designated product range(s) over its life cycle within a product portfolio of a business area in a manner that maximizes the overall return/profit to the company, within the context of company, business area and marketing plans. Ensures compliance with quality systems, regulatory requirements, and commercial change process.
2. Lead the commercial input to the product development process once the product definition is approved. Identify target market(s) for Product Models & Offerings.
3. Manages all aspects of the product (s) life cycle starting with the detailed planning phase (in development) until the product is terminated. Define Product Models and Structures. Identify Offerings Items & Structures.
4. Strategic and tactical supply management of existing products to market for multiple customers and applications.
5. Managing Platform Products fully recognizing the company benefit that can be obtained by facilitating the use of these for applications in other global business areas.
6. Maximizing the company profit over the product (s) entire life cycle.
7. Management of the cross-functional interface with product development and manufacturing.
8. Own the complete USP product portfolio- from lead generation to order closing and execution.
9. Working closely with regional managers across the country to provide support for USP product portfolio.
10. Work closely with customers in understanding the requirements and identifying the right product or product mix to meet the requirement.
11. Coordinate with global and local stake holders for successful execution of the project including FAT/SAT
12. Lead design-in activities for the reedy to process, filtration and bioreactor product portfolio.

Quality Specific Goals:
1. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position
2. Complete all planned Quality & Compliance training within the defined deadlines
3. Identify and report any quality or compliance concerns and take immediate corrective action as required
4. Lead quality: improve product reliability, implement and operationalize the QMS, zero enforcement actions through effective QMS management and inspection readiness.
5. Establish a commitment to quality and communicate the importance of meeting statutory, regulatory and customer requirements. Ensure quality policy is understood, implemented and maintained at all levels of the organization. Establish and communicate quality objectives that are measurable and consistent with the quality policy.
6. Maintain adequate organizational structures and adequate resources of sufficiently trained personnel. Ensure qualified personnel relative to assigned responsibilities. Ensure appropriate responsibility, independence and authority of all personnel who manage, perform and assess work affecting quality.

Required Qualifications: 
1.Master’s Degree in science/technology/Life Sciences/Biochemistry/Biotechnology/Microbiology with 6-10+ years of experience in biopharmaceutical industry in field of upstream operations.
2. Ph.D in Life Sciences/Biochemistry/ Biotechnology/ Microbiology with 4-7 years of experience in biopharmaceutical industry in field of upstream operations.
3. Excellent oral and written communications skills
4. Strong analytical and process skills
5. Strong project management skills
6. Strong communication skills
7. Ability to work effectively within a matrix environment

Candidate Profile
1. PhD in Biological Sciences, MBA
2.Prior hands-on experience in Upstream process development/manufacturing using single use technology.
3. CMO or Pharmaceutical Industry experience
4. Innovation – develop new ideas through collaboration and execute on creative ideas
5. Team oriented – ability to motivate and work well with diverse, cross-functional teams
6. Proven ability to work globally
7. Proven ability to influence and negotiate internally and with customers.

Additional Information:
Experience: 6-10 years
Job Number: 2640579
Location: Bangalore, India
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Product Management
End Date: 5th July, 2016

Required for Clinical Data Analyst III in Parexel

Post: Clinical Data Analyst III

Job Description
The role of the Clinical Data Analyst III (CDAIII) is to independently perform all clinical data processing activities from database set-up through database lock on assigned projects, commensurate with experience and/or project role. May also be responsible for coordinating a moderate team or multiple small size protocols as the Primary CDA, if assigned, with moderate to minimal supervision.

Candidate Profile
Moderate to considerable Clinical data management; clinical and/ or research experience with solid understanding of clinical trials methodology and terminology is desired.

Additional Information:
Location: Bangalore, Karnataka
Functional Area: CR
Requisition: pare-10047129
Industry Type: Pharma/ Biotech/Clinical Research
Employment Type: Full Time
Job Type: Regular
End Date: 16th May, 2016

Job as B.Pharm/B.Sc/D.Pharm as Office Executive in AvansCure LifeSciences

Post: Office Executive

Job Description
Office Executive work:
1. Call Interaction with clients /vendors
2. Responding mails of clients /vendors
3. Presentations
4. Data updates

Candidate Profile:
Required B Pharm /B. Sc. /D Pharm for Gurgaon (New Delhi) office, should be fluent in English, should have Good communication skills with knowledge of computer basics (internet, excel, word, pdf, ppt, etc.), Fresher can also apply.

Additional Information:
Location: India
Qualification: B.Pharm/B.Sc/D.Pharm
Functional Area: Other
Industry Type: Pharma/ Biotech/Clinical Research
Employment Type: Full Time
Job Type: Regular
End Date: 16th May, 2016

Phone: Mr. Ravi Balwani- 9828487490
Send your resume to info@avanscure.com

Recruitment of Product Specialist in Novo Nordisk | B.Pharm/B.Sc

Post: Product Specialist - India Affiliate

Job Description
About the department
Sales is responsible for the successful implementation of long term and short term marketing strategies in the field and establish true diabetes leadership in all therapies which caters to every segment in the society. Also ,the department maximises sales force effectiveness by implementing robust tools and processes. 

• You will join an ambitious team of field executives responsible for promoting our brand to doctors and conducting prescription audits.
• You will especially focus on increasing sales and market share by educating the users about benefits of our products.
• You will be given a number of different responsibilities and experience a variety of tasks,working with both internal and external stakeholders.

Qualification
You hold an academic degree in B Pharmacy /B Science with 1+ years of pharmaceutical sales experience. You have excellent communication & influencing skills. You are flexible and result oriented with a 'can-do' attitude. You must be prepared to invest significant personal effort in your work and proactively take ownership of your areas of responsibility. You are fluent in both written and spoken English.

Additional Information:
Experience: 1+ Years
Qualification: B.Pharm, B.Sc
Industry Type: Pharma/ Biotech/Clinical ResearchFunctional Area: Field Sales 
Location: Faridabad-Haryana
Requisition ID: 38634BR
Last Date: 2 April 2016