Medtronic Looking For Clinical Research Monitor(CRA)

Medtronic Released Job Openings On 27/11/2021.Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be..Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details are provided below. Interested and eliible candidates can  submit application along with resume. 

Vacancy Details:

Medtronic Recruiting B.E or B.Tech (Bio Medical Engineers / Bio Technology)/ B. Pharma /Bachelor’s Degree in Sciences from an accredited university.M.Tech ( Bio Medical Engineers / Bio Technology)/ M.Pharma/ Masters Bachelor’s Degree in Sciences from an accredited university / MBA Bio Technology Candidates with 3 to 7 Years experience in Clinical research and Monitoring field for Clinical Research Monitor(CRA) Position.Complete Details for the Clinical Research Monitor(CRA) as follows.

Important Details :

• Location : Gurgaon
• No of Vacancies:01 Or More
• Details of Salary: NA.
• Opening date for online Application: 27/11/2021
• Mode of application :Online
• How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps

Related Job: Torrent Pharmaceuticals Walk In 28th Nov 2021 For B. Sc,B. Pharm,M.Sc,M. Pharm 

Job Description/Skills Required

Medtronic Clinical research teamgives the opportunity for an incumbent to be part of clinical trials at the site and headquater level and focus on developing efficient clinical practices.

• Monitors progress of clinical trials at the site level or headquarters and ensures that they are conducted, recorded and reported in accordance with the protocol, standard operating procedures (SOP), good clinical practices (GCP), and other applicable regulatory requirements.
• Develops and maintains liaison with clinical investigators, clinical research organizations (CRO), affiliated hospitals, and research institutions to initiate and expedite clinical studies on products that have investigational new drug or medical devices approval.
• Responsible for reviewing adverse event cases with investigators, determining and monitoring time, budget, schedules, preparing study documents, and issuing status reports.
• May assist with design, development, and monitoring of clinical evaluation projects.
• Trains investigators and site personnel.
• Includes headquarter and field clinical research associates (CRA).
• Implements and prepares the clinical development strategy as outlined by the clinical teams.
• May contact and recommend qualified investigators to perform studies and initiate clinical trials.
• Ensures recruitment and retention of patients.

Nice to Have

• Manage projects assigned and works with other stakeholders to achieve desired results.
• Deliver and oversee the projects – from design to implementation – while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education.
• Strong learning agility and problem solving skills.
• Demonstrates integrity and recognized as a role model by their peers and manager.
• Strong interpersonal and presentation skills.
• Highly optimistic and indomitable spirit.
• Excellent communicator with a good command of written and spoken English.
• Excellent computer skills with experience of Microsoft Word/ Outlook/ Excel/ PowerPoint.
• Willingness to travelGood interpersonal skills.

Click here for Official notification and Apply