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4 Job openings at Croissance Clinical Research
Business Development

India

0 years

INR Not disclosed

On-site

Full Time

Basic Function and Scope of Responsibilities To develop marketing materials including website, brochures, banners/ back-drops, newsletters, power-point presentations, email marketing. Management of company website, social media pages and online marketing/ advertisement. Brand Building, launching and executing pre/on/post conference campaigns. Provide Inputs/Develop presentation for bid defense of proposals. Persistent follow up with prospects and clients. Responsible for all brand promotion activities, brand visibility and popularity. Support in updating of database, collating data and documents for marketing. Regular updates of the Pharma and CRO industry to the BD team and assist them in research and development activities. Planning, coordinating and hosting all the business meetings. Responsible for all kind of security issues. To prepare the list of important domestic and international conferences and working toward the registration for short listed conferences. Establish and develop a relationship with the customer organization Sales calls (Dealing directly with customers through telephone. Responding promptly to customer inquiries) & Market Research Qualifying the customer and generates sales as well generate lead. Determine new opportunities which include project sales as well as staff augmentation based on customer need. Perform potential client research through cold callings, mailings and business conversation through social media. Listen attentively to clients need and give proper solutions. Responsible for calling prospective clients & explain them about the services. Responsible to leverage on the existing customer base and expand into the US market. Job Types: Full-time, Permanent Benefits: Provident Fund Schedule: Day shift Monday to Friday Supplemental Pay: Yearly bonus Language: English (Preferred) Work Location: In person Application Deadline: 15/06/2025

Senior Driver

India

0 years

INR 0.22 - 0.23 Lacs P.A.

On-site

Full Time

Job Summary: We are seeking a reliable and experienced Senior Driver to manage and carry out driving assignments with professionalism and safety. The Senior Driver will be responsible for operating company vehicles, transporting goods or personnel, training junior drivers, and ensuring all transport operations comply with safety and traffic regulations. Key Responsibilities: Operate company vehicles (e.g., light or heavy-duty vehicles) in a safe and efficient manner. Transport personnel, goods, or materials to designated locations as scheduled. Maintain vehicle cleanliness, functionality, and report mechanical issues promptly. Keep accurate logs of mileage, fuel use, and maintenance. Mentor and supervise junior drivers, offering guidance and on-the-job training. Ensure compliance with company policies, traffic laws, and safety standards. Coordinate with logistics or dispatch teams for scheduling and delivery tasks. Assist in route planning to optimize time and fuel efficiency. Handle minor vehicle troubleshooting and first-aid emergencies if required. Represent the company professionally when interacting with clients or partners. Qualifications: High school diploma or equivalent. Valid [Insert Country/State] driver’s license appropriate for vehicle type (e.g., CDL for heavy vehicles). Minimum [X] years of professional driving experience, including long-distance or high-profile assignments. Clean driving record with no major traffic violations. Job Types: Full-time, Permanent Pay: ₹22,000.00 - ₹23,000.00 per month Benefits: Provident Fund Schedule: Day shift Work Location: In person Application Deadline: 19/06/2025 Expected Start Date: 18/06/2025

Clinical Data Manager

Hyderābād

0 years

INR 1.8 - 3.515 Lacs P.A.

On-site

Full Time

Organizing Kick-off meetings with the client co-ordination with the functional Head.  Responsible for allocating the project/Study to team members.  Responsible for Review and Internal approval of Data Management Plan (DMP), Case Report Form (CRF), and Edit check Specification Document (ESD).  Responsible for Review and Internal approval of Data Entry Guidelines, Self-Evident Correction Document (SEC).  Internal approval of Annotated CRF (aCRF) and Functional Design Specification (FDS) Document.  Responsible for preparing and training the SOP’s.  Responsible for approval of database screens, Edit checks designed in database and DCF/Query tracker.  Internal Quality Control for all Data Management Documents like Data Management Plan, Annotated CRF, Functional Design Specification Document, and Edit check Specification Document.  Responsible for Issuing the Database Test Certificate.  Responsible for Database Lock and Unlock procedures.  Responsible for exporting the data to SAS team for analysis.  Responsible for Review and approval of Master Data Management File (MDMF).  Responsible for Data Management Presentation in Investigator meeting.  Providing inputs for proposal development in co-ordination with the Function Head Job Types: Full-time, Permanent Benefits: Provident Fund Schedule: Day shift Work Location: In person Application Deadline: 22/06/2025

Manager Clinical Operations

India

0 years

INR 1.88976 - 6.972 Lacs P.A.

On-site

Full Time

· Training the teams and new employees regularly and periodically. · Negotiating the study budgets with the Principal Investigator and executing the Clinical Trial Agreement. · Assigning and Managing the project team as per the study requirement. · Development and Revision of departmental SOPs. · Reviews CRA Site Visit documents (follow up letters and reports). · Reviews and Approves the travelling plan and budgets of the monitors. · Updating the sponsor about the progress of the study as agreed in the contract. · Participating in telecoms with the clients and kick of meetings. · Hosting the external audits. · Preparing Monitoring plan for the CRA as per the study specifications and protocol and training the CRA on the same. · Training the team on study related documents. · Managing and coordinating all regional CRA activities. · To perform co-monitoring visits to ensure quality of data generated · If required accompanying the CRA’s in Qualification visit, Site Initiation Visit and Monitoring visits. · Organize and present at Investigator Meetings/ Internal meetings. · Development of project management plan, risk management plans. · Review the Ethics Committee dossiers as required. Review of power point presentations prepared by CRA for investigator meetings, Site Initiation visits. Job Types: Full-time, Permanent Pay: ₹15,748.50 - ₹58,100.22 per month Benefits: Provident Fund Schedule: Day shift Work Location: In person Application Deadline: 30/06/2025 Expected Start Date: 07/07/2025

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