WhatsApp Group Join Now
Telegram Group Join Now

Job highlights

Work/Life Balance

Time management

Flexibility

Problem Solving

The Clinical Project Manager will serve as the primary contact between sponsors and the organization, ensuring smooth execution of research projects. Below is an overview of the key responsibilities:

Project Management

  • Plan, execute, monitor, and complete clinical research projects across therapeutic areas.
  • Ensure all activities comply with regulatory, corporate, and sponsor requirements.
  • Develop project plans, timelines, and risk management strategies using established processes and tools.
  • Oversee financial, operational, and regulatory compliance to ensure project integrity.

Document and Tool Management

  • Coordinate with cross-functional teams to manage project-related tools and documents such as protocols, SOPs, and informed consent forms.
  • Prepare project reports and investigator updates throughout the project lifecycle.
  • Ensure proper data collection, storage, and disposal according to regulatory standards.

Team Management and Performance

  • Assign and monitor project tasks, including site monitoring, data management, safety management, and statistical analysis.
  • Ensure tasks meet quality standards and align with client and regulatory expectations.
  • Facilitate communication and performance within the project team to ensure seamless project delivery.

Client and Sponsor Support

  • Act as the primary liaison with sponsors, managing expectations and addressing concerns.
  • Plan and coordinate project meetings and assist in patient recruitment strategies.
  • Develop stakeholder training materials and provide regular project status updates to sponsors.

Qualifications

To be eligible for this role, candidates should meet the following qualifications:

  • Education:
    • Minimum of a three-year Advanced Diploma/Degree in Health Sciences, Clinical Research, or a related field.
  • Experience:
    • 1-3 years of relevant work experience in clinical trials, project management, or regulatory submissions.

Key Skills Required

  • Project Management Expertise: Experience in regulatory submissions, clinical trial management, and risk management.
  • Communication Skills: Ability to communicate effectively with clients, sponsors, and team members.
  • Detail-Oriented: Keen attention to detail to ensure accuracy in project documentation and processes.
  • Teamwork and Collaboration: Ability to foster a collaborative working environment.
  • Continuous Learning: Willingness to engage in self-development and improve skills.
  • Language Skills: Proficiency in English (reading, writing, and speaking).

This is a remote position, offering flexibility to work from home. The role involves managing multiple projects and collaborating with team members across locations.

Application Link

Featured Courses

1

CLINI INDIA

Interactive Brokers Logo

Coupon:

CLINIBHARAT (10% Discount)

Courses:

  • Data Management
  • Pharmacovigilance
  • Medical Writing
  • Medical Coding
  • Regulatory Affairs
  • Clinical Research
2

CLINIVERSITY

Interactive Brokers Logo

Coupon:

MONSSOON (20% Discount)

Courses:

  • Data Management
  • Pharmacovigilance
  • Medical Coding
  • Clinical Research
3

CLINIWINGS

Interactive Brokers Logo

Coupon:

WINGS (10% Discount)

Courses:

  • Clinical Data Management
  • Pharmacovigilance
  • Medical Writing
  • Regulatory Affairs
  • Clinical Research
Best Placements in Pune
X