Urgent Requirement on Technical Project Manager - Web @ Richmond, Virginia

Hello Dear, Greetings.

This is Chandra from Nixsol Inc.,

 

We have an Urgent Requirement on  Technical Project Manager - Web  

 

Technical Project Manager - Web  

Location : Richmond, Virginia 

Duration : 1 + Year  

 

Job Description:
A project Manager will work with Client  to develop Microsoft Project Plan to track transition applications and websites from one vendor to multiple vendors.  The PM will need excellent communication skills, application development knowledge.  Must be excellent working in team environment, working with customers, and be able to handle some decision making.  

Skills:
2-5 years demonstrated Project Management to include the following

·         to coordinate activities to meet project deadlines and budgets.

·         Knowledge of BA skills for understanding an documenting user requirements.

·         Position requires extensive knowledge and leadership experience in web applications; development, tools, and software, including payment processing protocols.

·         Ability to work with technical and non-technical people often conveying complex technical information.

·         Excellent verbal communication skills.

·         Experience in working on multiple projects with an extensive variety of stakeholders and multiple vendors.

·         Demonstrated skills in building effective, professional relationships across a broad spectrum of roles including customers, stakeholders, technical teams, and vendors.

·         Knowledge of web and payment portals, payment methods, electronic gateways, and associate web tools.  

·         Knowledge of system architectural design of hardware for hosting environments required to support web applications.

 

ü  5-10 years - demonstrated ability to use Microsoft Office such as Microsoft Excel.
5-10 years Application development to include the following

ü  Knowledge of the following tools/platforms:  Perl 5; Visual Studio 2003, 2005, 2008, 2010; Adobe Captivate; Adobe Life Cycle, or equivalent tools.

ü  Practiced in the following programming languages:  VB.Net; C#.Net; Asp; Flex

ü  Knowledge of Database such as Informix, SQL, Oracle and familiar with database normalization.

Education and certifications
Degree in information technology or related field desirable; other education and/or progressive experience may substitute.
PMP certified at least 2 years - (Must be current). 

 

Give me the details listed below:

Full Name:
Availability to start-----:
Availability for interview:
Visa Status (US Citizen, GC Holder, H1b or TN holder): 
Contact Number:
E-mail Address:
Re-location:
Current Location (Place & State):
Last 4 SSN:
(Date of Birth) Date & Month:
2 Professional References  (Name/ Project Name/ Title/Email ID/ Contact number):

 

Regards,
Chandra K.

Nixsol Inc.,
53 Knightsbridge Road

Suite # 216

Piscataway, NJ 08854.
(:(732)-832-7933
6:(732)-909-2424
*:chandra@nixsol.com

Gtalk & IM: AccMgrInUSA

Open Jobs : Nixsol Jobs Blog

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Direct Client Urgent Requirement on Lead Clinical Data Managers @ East Hanover, NJ

Hello Dear, Greetings.

This is Chandra from Nixsol Inc.,

 

We have an Urgent Requirement on  Lead Clinical Data Managers

 

LEAD CLINICAL DATA MANAGERS

Location: East Hanover, NJ

 

To Lead and Manage project activities at Study level at assigned client sites for Clinical Data Management and ensure efficient coordination among Study Teams and Data Management Teams.

 

JOB SPECIFICATIONS

 

1. Qualification

Graduate / Post-Graduate degree in Life Sciences/ Pharmacy/Project Management

Over 6 years of total experience with organization including over 3-5 years as a clinical data manager.

 

2. Special Skills and Knowledge

ICH - Good Clinical Practice

Detailed breadth of CDM experience and knowledge

Understanding of clinical trial and systems regulations for key health authorities

Ability to lead/supervise a team as well as mentor / direct team members

Overall advanced knowledge of Clinical Trial Methodology

Advanced Project Management Skills experience

Good knowledge of drug development process

Demonstrated strong focus on Quality

Demonstrated ability to support team members through Coaching & Mentoring

Good attention to Detail

 

Key Competencies

Leadership

Listening, Communication

Negotiation / Influencing

Communication Skills – Written & Verbal

Problem Solving & Decision Making

Risk Management

Proactive

Flexible

 

JOB ROLE

 

Key Accountabilities:

- Act as a single point of contact for all data management center deliverables during the Study Set-up, conduct and close-out phases

- Create/Provide input to project Data Management Plan

- Provide input/review the DM components in the protocol.

 

Creation of the Case Report Form from global standards and creation of protocol specific case report form modules by coordinating with sponsor’s protocol team and review of the same

 

- Accountable for the creation/review/maintenance of the CRF completion guidelines, edit check specifications leveraging global standard validations

- Accountable for database review, testing and UAT of edit checks for assigned studies

- Accountable for monitoring study progress and timely locking and freezing of database.

- Responsible for Project Management of the study and accountable for all study deliverables from end to end.

- Ensure adherence to Client SOPs

- Provide guidance and supervision to the study teams.

- Clarify, manage and successfully implement customer expectations, resolving conflicts whilst pursuing win-win scenarios

- Monitor quality and efficiency across functions to identify trends and opportunities for improvements. Ensure sharing of learning across geographies

- Manage relationships with Client at both the operations level and with functional peers

- Ensure project milestones are met according to agreed upon timelines with high quality

- Coordinate and work closely with offshore Trial Data Managers/Therapeutic Area Managers to ensure that study deliverables are met as per the timelines and with high quality.

- Review resource estimates for data management activity for allocated studies

- Participate in Study Kick Off meetings and lead all study related meetings during the Study Set-up phase /Conduct/Close out.

- Support both protocol and procedural training to external vendors and investigator’s site whenever required

- Coordinate to provide support for Data Safety Monitoring Board and all other vendors including Investigator’s site and the clients internal teams

- Act the as primary contact for all data management problems, issues and questions from study teams and be responsible for issues resolutions

- Responsible for tracking the various data management activities using study reports/metrics.

 

Give me the details listed below:

Full Name:
Availability to start-----:
Availability for interview:
Visa Status (US Citizen, GC Holder, H1b or TN holder): 
Contact Number:
E-mail Address:
Re-location:
Current Location (Place & State):
Last 4 SSN:
(Date of Birth) Date & Month:
2 Professional References  (Name/ Project Name/ Title/Email ID/ Contact number):

 

Regards,

Chandra

Nixsol Inc.|  53 Knightsbridge Road Suite # 216 |  Piscataway, NJ 08854. | Open Jobs : Nixsol Jobs Blog

Office: (732)-832-7933 |  Fax: (732)-909-2424 |  Email: chandra@nixsol.com   | Gtalk : AccMgrInUSA |  www.nixsol.com 

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