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Global Project Management

0-1 years
1.75-2 Lacs P.A.
10 Jan. 8, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Position: Project Manager
Industry Type: Clinical Research / Contract Research
Department: Project & Program Management
Employment Type: Full-Time, Permanent
Role Category: Other Program / Project Management

Role & Responsibilities:

  • Strong planning and organizational skills, with the ability to manage multiple priorities independently.
  • Build and maintain effective relationships with all functional units across all Cliantha Research sites.
  • Knowledge of basic regulatory guidelines for conducting BA/BE studies.
  • Excellent customer service skills and the ability to understand and apply technical manuals.
  • Create, plan, and monitor all project activities in the PM database, ensuring accuracy at all times.
  • Identify interdependencies for all projects and facilitate communication among functional areas as needed.
  • Understand the time-sensitive nature of critical path project activities and notify relevant teams and management of issues.
  • Work with management to establish project interim milestones and ensure projects stay on schedule, including reporting structures like CS-BE and FDA tables.
  • Provide first-level support for software problems related to the PM database and document issues and solutions.
  • Solicit feedback from end users to ensure the database meets the organization’s needs.
  • Identify opportunities and recommend solutions to enhance or improve current business processes.
  • Provide basic training to end users on the PM database, including cross-functional training.
  • Maintain and update analytical methods and bioequivalence studies on a monthly basis.

Preferred Candidate Profile:

  • Knowledge in BA/BE Studies with excellent English communication skills (Mandatory).
  • This opportunity is open to freshers, preferably based in Ahmedabad or Gujarat.

Educational Qualifications:

  • UG: B. Pharma (Any Specialization)
  • PG: M. Pharma (Any Specialization)

Key Skills:

  • BA/BE Studies
  • Clinical Research
  • Clinical Operations
  • GLP (Good Laboratory Practice)
  • Clinical Trials

About Cliantha Research:
Cliantha Research is a Clinical Research Organisation (CRO) providing global clinical trial solutions with a commitment to quality and regulatory compliance.

Company Info:

  • Address: TP 86, FP 28/1, Cliantha Corporate, Ahmedabad, Gujarat, India