Senior Clinical Trial Manager

Abbott Healthcare · Mumbai · onsite · Posted 24d ago

Not disclosedFresherfulltimeSourced from Foundit

About a minute. You'll make an account on the way through.

About this role

JOB DESCRIPTION:

Plan, coordinate and oversee all start-up activities of internal disciplines (Drug supply, Regulatory, Safety, Data Management etc.) and being the main contact (supervise, steer etc.) for involved CROs and other external vendors, if applicable
Agree and/or ensure implementation of study principles and deliverables (safety, timelines, quality, milestones, budget, etc.) and follow-up to guarantee adherence
Facilitate communication and ensure adequate collaboration between all involved parties
Communicate effectively processes to in-/external service groups and clients in accordance with all applicable procedures (e.g. BIOM, Task List etc.)
Participate in teams related to trial conduct (e.g. Clinical Study team, Extended Joint Abbott- CRO Clinical Team, Drug supply team etc.) and organize/attend external key study meetings (Kick-off meeting, CRA meeting, Investigator meeting, etc) as applicable
Read, review and/or assist in preparation of core project documents (e.g. Investigator Brochure, Concise Clinical Development Plan, Protocol, Informed Consent Form) as applicable
Review key Clinical Trial Management strategies like: Communication plan / Feasibility / Patient & Site recruitment / Drug supply / EC&RA Submission, etc.

Oversee and manage with the CRO Project Manager the study conduct in order to ensure adequate and timely delivery of study data and documentation in Trial Master File (TMF):

Use efficiently tools to monitor status of e.g. patient recruitment and take corrective action if necessary
Ensure respect of agreed deliverables, and communicate efficiently within the teams (timelines, milestones, budget, quality)
Co-coordinate timely availability of all supplies important for the conduction of trials, including the re-supply of sites
Monitor data collection, cleaning and data transfer with respect to completeness, quality and timely delivery of the final results
Review audit reports and ensure issues are resolved
Participate in strategic decision making to improve recruitment
Apply operational risk management plan (if applicable)
Support activities to generate study report / dossier
Supervise and monitor the transfer and archiving of the clinical file (e.g. TMF)

The base pay for this position is

N/A

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Clinical Affairs / Statistics

DIVISION:

EPD Established Pharma

LOCATION:

India Mumbai : Mumbai Development Center - EPD

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

Not specified

MEDICAL SURVEILLANCE:

Not Applicable

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

Sourced from foundit

Skills

Drug supplyPatient Site recruitmentOperational Risk Managementregulatorydata transferClinical Trial ManagementfeasibilityData Collectioncommunication planSafety data management

JOB DESCRIPTION:

Plan, coordinate and oversee all start-up activities of internal disciplines (Drug supply, Regulatory, Safety, Data Management etc.) and being the main contact (supervise, steer etc.) for involved CROs and other external vendors, if applicable

Agree and/or ensure implementation of study principles and deliverables (safety, timelines, quality, milestones, budget, etc.) and follow-up to guarantee adherence

Facilitate communication and ensure adequate collaboration between all involved parties

Communicate effectively processes to in-/external service groups and clients in accordance with all applicable procedures (e.g. BIOM, Task List etc.)

Participate in teams related to trial conduct (e.g. Clinical Study team, Extended Joint Abbott- CRO Clinical Team, Drug supply team etc.) and organize/attend external key study meetings (Kick-off meeting, CRA meeting, Investigator meeting, etc) as applicable

Read, review and/or assist in preparation of core project documents (e.g. Investigator Brochure, Concise Clinical Development Plan, Protocol, Informed Consent Form) as applicable

Review key Clinical Trial Management strategies like: Communication plan / Feasibility / Patient & Site recruitment / Drug supply / EC&RA Submission, etc.

Oversee and manage with the CRO Project Manager the study conduct in order to ensure adequate and timely delivery of study data and documentation in Trial Master File (TMF):

Use efficiently tools to monitor status of e.g. patient recruitment and take corrective action if necessary

Ensure respect of agreed deliverables, and communicate efficiently within the teams (timelines, milestones, budget, quality)

Co-coordinate timely availability of all supplies important for the conduction of trials, including the re-supply of sites

Monitor data collection, cleaning and data transfer with respect to completeness, quality and timely delivery of the final results

Review audit reports and ensure issues are resolved

Participate in strategic decision making to improve recruitment

Apply operational risk management plan (if applicable)

Support activities to generate study report / dossier

Supervise and monitor the transfer and archiving of the clinical file (e.g. TMF)

The base pay for this position is

In specific locations, the pay range may vary from the range posted.