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Sunday, February 11, 2018

Multiple Clinical Jobs

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Entry - Experienced Biostatisticians, Medical Writers, Medical Editors, Statistical Programming, QC Auditors, Resulting Administrators, Document Review, Clinical Applications Programmer, Clinical Data Processor, Kit Inventory, DBSS, Clinical Project Adminstrator

To Apply this job get in touch with our team - 8892773842

Senior Project Manager - Clinical Ops

Covance Inc
 9 - 14 yrs
    Clinical Development Services, Early Clinical Development (ECD)
    Reports to Title: Any leadership position with ECD (Manager to Executive Director level)

    The statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job.

    I. Job Summary:
    Oversees and manages domestic and/or international clinical trials under leadership direction. Responsibilities typically include developing and managing budgets, timelines, and quality guidelines for projects, thereby ensuring that expectations are met while identifying and mitigating risks. The Senior Project Manager also compiles and drives documentation for the project, ensuring the accuracy and quality of regulatory data.

    Essential Job Duties:
    Lead core project team and facilitate teams ability to lead extended/complete project team. Depending on size and scope of project, this job duty may be performed in collaboration with a Project Director.
    Ensure effective cross-functional teamwork among project team members including both internal and external ancillary services. 
    Serve as escalation point for project issues.
    Resolve conflicts as needed.
    Lead implementation of Six Sigma initiatives on projects as applicable.
    Monitor project schedule and scope to ensure both remain on track. Initiate and implement appropriate actions.
    Proactively engage in both quality assurance and risk management activities to ensure project deliverables are met according to both Covance and client requirements.
    Accountable for budget across assigned project(s) including the control and minimizing of write-offs. Proactively identify out of scope activities and execute necessary change orders. 
    Collaborate with finance to initiate monthly invoicing.
    Ensure that all staff allocated to assigned project(s) adheres to professional standards and SOPs.
    Initiate improvements to enhance the efficiency and the quality of the work performed on assigned projects.
    Provide performance feedback of team members to respective supervisors.
    Present at external and/or internal meetings. 
    Ensure client satisfaction.
    Define and manage project resource needs and establish succession plans for key resources. 
    Create required project plans. Implement and monitor progress against project plans and revise as necessary. 
    Responsible for appropriate issue escalation to CAIR program and/or appropriate stakeholder(s).

Immediate Requirement of Clinical Process Associate @ Bangalore

Job Description

Greetings from Technosoft Corporation !!

Immediate requirement for Clinical Process Associate at  Bangalore 

Work Location - Bangalore

Experience 0.6 months to 3 Years (In clinical research/ Patient Data Reviewing)

Contact: VANI B (9182991774) 

Candidate who are interested in the profile do share your CV/Resume at / or can drop text/call on 9182991774 

Skills required - CRC knowledge, Patient Data knowledge, ICH - GCP, ICF, Adverse Events/ SAEs, site monitoring, remote site monitoring knowledge. (eTMF - experience - not mandatory but preferred). 


Provide project related assistance for assigned complex project(s), sites and project teams. Ensure all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements and meets quality and timeline metrics.


  • Perform complex processes and tasks that eventually result in high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines
  • Establish and maintain effective project/ site communications 
    Create and maintain relevant project documents
  • Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information
  • Participate in document management (creation, review, maintenance, storage, as applicable)


  • Good knowledge of applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines
  • Strong written and verbal communication skills including good command of English language
  • Results and detail-oriented approach to work delivery and output
  • Good problem solving skills
  • Good planning, time management and prioritization skills
  • Attention to detail and accuracy in work
  • Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.
  • Proven ability to work on multiple projects balancing competing priorities
  • Ability to coach/ mentor junior colleagues

Schedule interview : If above Requirements matches to your profile can send your updated CV to / and reach at  9182991774 (drop me a text message)*

Regulatory Affairs Associate

  • To prepare applications to Marketing authorization and clinical trial. Support team for preparation of dossier for timely submissions to the regulatory authorities. 
  • Compile clinical trial applications, Import & export license submission, approval and maintenance for clinical trials per local regulations, ensuring timely submissions, follow-up with and approval from the regulatory authorities
  • Respond to regulatory queries seeking support and feedback from appropriate functions within Organization
  • Ensure regulatory compliance by managing regulatory submissions for notification and/ or approval during the course of the execution of each clinical study including preparation and submission of annual study status reports and study completion reports
  • Ensure timely registration and maintenance of all approved clinical trials in the Indian clinical trials registry (CTRI)
  • Ensuring that local labeling requirements are developed in alignment with local regulatory requirements and Organization standards
  • Participate in process improvement initiatives, and recommend process changes where necessary 

Desired Candidate Profile

    • Education: Bachelors degree or Master degree in Life Sciences or equivalent or B Pharm or M Pharm 
    • 2- 5 years of related professional experience in the pharmaceutical / biotechnology pharmaceutical or medical device industry for India registration 
    • Worked on Form 44, New Drug application for P II-II trials
    • Experience in Regulatory Affairs activities such as Preparing applications, dossiers of clinical trials, Import & export license submission, 
    • Working experience for DCGI operations
    • Knowledge of Indian regulations, directives and guidelines related to Organizations products and operations preferred. 
    • Good working experience in MS Office 
    • Strong oral and written communication skills.

 Senior CRA reqd: Qual: Tertiary qual in related science/healthcare discipline; Exp: 3+ yrs of proven Clinical Monitoring experience with CRO/ Pharma; Location: Bangalore.
 If interested please send CV to `’.

 Opening at Mumbai

Profile requirement

1.   Experience: 6-7 years

2.   Preferably SAP certified.

3.   Implementation projects: 3 – 4

4.   Sound business process knowledge

5.   Client facing role. Can manage client interaction independently.

6.   Good communicator in English.

7. Necessary to have good Funds Management expertise

Location-  Mumbai( Koparkhairane)

Pls share resume to

[1:52 PM, 2/11/2018] Ravindr CR W GROUP:
We have urgent requirement of MBBS and MD pharmacology for pharmacovigilance department in Mumbai based pharma big organisation

Location Mumbai very urgent hiring

Send m CV on

Company: Lupin

[2:02 PM, 2/11/2018]  We have urgent requirement of MBBS and MD pharmacology for pharmacovigilance department in Mumbai based pharma big organisation
Location Mumbai very urgent hiring
send m CV on
 Hiring !!!!!!! Dehradun ( Uttarakhand ) Based Pharmaceutical Company Looking President-Operation Manager along with Production, Quality Assurance, Quality Control, Production, Formulation Development, Regulatory Affairs Department
All level candidate welcome
Location: Dehradun and Gurgoan