Current jobs related to Clinical Research Associate - Karad - Fusion Business Solutions Pvt. Ltd.

  • Research Project Coordinator

    7 days ago

    Karad, Maharashtra, India beBeeClinicalTrial Full time ₹ 30,08,600 - ₹ 40,00,671

    Job Title: Research Project Coordinator">We are seeking a highly organized and detail-oriented professional to coordinate clinical trials. The successful candidate will be responsible for planning studies, ensuring compliance with regulatory requirements, and providing excellent support to research staff.">Study Planning: Assist in developing study...

  • Medical Officer

    1 week ago

    Karad, India Fusion Market Research Full time

    **.**.We are seeking a highly capable medical officer to manage our medical team and to supervise the healthcare services that they provide. In this role, your duties will include serving as a clinical advisor, overseeing clinical trials, and maintaining high standards of inpatient care. To ensure success, medical officers should exhibit extensive clinical...

  • Medical Coding

    4 days ago

    Karad, India Statistical Pharma Full time

    **Medical Coder Job Responsibilities**: - Accounts for coding and abstracting of patient encounters, including diagnostic and procedural information, significant reportable elements, and complications. - Researches and analyzes data needs for reimbursement. - Analyzes medical records and identifies documentation deficiencies. - Reviews and verifies...

Clinical Research Associate

2 weeks ago

Karad, India Fusion Business Solutions Pvt. Ltd. Full time

*Job Description*
As a Clinical Research Associate (CRA), you will play a vital role in the planning, executing, and monitoring clinical trials conducted within our organization. Working closely with our research teams, you will ensure compliance with regulatory requirements, adherence to study protocols, and the collection of high-quality clinical data.

*Responsibilities*
- Assist in the preparation of study protocols, informed consent forms, and other essential study documents.
- Identify and evaluate potential clinical trial sites, ensuring they meet protocol requirements and regulatory standards.
- Conduct site initiation visits to train site staff on study protocols, procedures, and data collection methods.
- Oversee the collection, documentation, and verification of clinical trial data in accordance with study protocols and regulatory guidelines.
- Ensure compliance with Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, and applicable regulations.
- Collaborate with cross-functional teams, including clinical operations, data management, and regulatory affairs, to support the successful execution of clinical trials.

**Qualifications**:*
- Bachelor's or Master's degree in Pharmacy (B.Pharm/M.Pharm) or Life Sciences (BSc/MSc).
- Effective communication and interpersonal skills.
- Knowledge of regulatory requirements and guidelines governing clinical research is a plus.

**Job Types**: Full-time, Permanent, Fresher

Pay: ₹15,985.98 - ₹45,131.51 per month

**Benefits**:

- Health insurance
- Provident Fund

Schedule:

- Day shift
- Morning shift

**Experience**:

- total work: 1 year (preferred)

Work Location: In person